Use of Anthrax Vaccine in the United States: Recommendations of the Advisory Committee on Immunization Practices, 2019
Recommendations and Reports / December 13, 0019 / 68(4);1–14
William A. Bower, MD1; Jarad Schiffer, MS2; Robert L. Atmar, MD3; Wendy A. Keitel, MD4; Arthur M. Friedlander, MD5; Lindy Liu, MPH1; Yon Yu, PharmD6; David S. Stephens, MD7; Conrad P. Quinn, PhD8; Katherine Hendricks, MD1 (View author affiliations)View suggested citation
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- Risk for Exposure to Anthrax
- Summary of Key Findings
- Recommendations for Prevention of Anthrax Among Persons with Potential Risk for Exposure: PrEP
- Recommendations for Prevention of Anthrax Among Persons with Suspected or Known Exposure: PEP
- Vaccine Adverse Events Reporting and Additional Information
- Future Directions
- Advisory Committee on Immunization Practices
- ACIP Anthrax Vaccine Work Group
This report updates the 2009 recommendations from the CDC Advisory Committee on Immunization Practices (ACIP) regarding use of anthrax vaccine in the United States (Wright JG, Quinn CP, Shadomy S, Messonnier N. Use of anthrax vaccine in the United States: recommendations of the Advisory Committee on Immunization Practices [ACIP)], 2009. MMWR Recomm Rep 2010;59[No. RR-6]). The report 1) summarizes data on estimated efficacy in humans using a correlates of protection model and safety data published since the last ACIP review, 2) provides updated guidance for use of anthrax vaccine adsorbed (AVA) for preexposure prophylaxis (PrEP) and in conjunction with antimicrobials for postexposure prophylaxis (PEP), 3) provides updated guidance regarding PrEP vaccination of emergency and other responders, 4) summarizes the available data on an investigational anthrax vaccine (AV7909), and 5) discusses the use of anthrax antitoxins for PEP.
Changes from previous guidance in this report include the following: 1) a booster dose of AVA for PrEP can be given every 3 years instead of annually to persons not at high risk for exposure to Bacillus anthracis who have previously received the initial AVA 3-dose priming and 2-dose booster series and want to maintain protection; 2) during a large-scale emergency response, AVA for PEP can be administered using an intramuscular route if the subcutaneous route of administration poses significant materiel, personnel, or clinical challenges that might delay or preclude vaccination; 3) recommendations on dose-sparing AVA PEP regimens if the anthrax vaccine supply is insufficient to vaccinate all potentially exposed persons; and 4) clarification on the duration of antimicrobial therapy when used in conjunction with vaccine for PEP.
These updated recommendations can be used by health care providers and guide emergency preparedness officials and planners who are developing plans to provide anthrax vaccine, including preparations for a wide-area aerosol release of B. anthracis spores. The recommendations also provide guidance on dose-sparing options, if needed, to extend the supply of vaccine to increase the number of persons receiving PEP in a mass casualty event.
Anthrax is an acute febrile illness caused by infection with Bacillus anthracis. The mortality rate, even with treatment, ranges from <2% for cutaneous anthrax (1) to 45% for inhalation anthrax (2) and 92% for anthrax meningitis (3). B. anthracis is a zoonotic pathogen that primarily infects sheep, goats, cattle, and other herbivores. Humans become infected after exposure to infected animals or contaminated animal products or, rarely, as a complication from injection drug use (4). B. anthracis is also a tier 1 select agent and is considered one of the bioterrorism agents that is most likely to be used because it is relatively easy to acquire from the natural environment, mass produce, and disseminate as spores via aerosolization (5).
Anthrax vaccine adsorbed (AVA) (BioThrax) is licensed for preexposure prophylaxis (PrEP) for adults aged 18–65 years at high risk for exposure to B. anthracis (6). The dosage approved by the U.S. Food and Drug Administration (FDA) is 0.5 mL administered intramuscularly (IM) at 0, 1, and 6 months with boosters at 6 and 12 months after completion of the primary series and at 12-month intervals thereafter. AVA also is licensed for postexposure prophylaxis (PEP) in combination with antimicrobials for adults aged 18–65 years with suspected or known exposure to aerosolized B. anthracis spores. The dosage approved by FDA is 0.5 mL administered subcutaneously (SC) at 0, 2, and 4 weeks. For persons not included in the FDA-approved indication for PEP, AVA will be available for PEP use for children, pregnant women, nursing mothers and older adults (i.e., ≥66 years) under appropriate emergency use regulatory provisions. Although data are lacking on the immune impact of mixing the IM and SC routes of administration, as might occur when switching from PrEP to PEP, switching between routes would be unlikely to adversely impact immunity because both routes provide adequate immunity.
AV7909 (AVA plus CpG 7909 adjuvant) is a second-generation anthrax vaccine produced by Emergent BioSolutions that is in a phase 3 trial (https://clinicaltrials.govexternal icon). The CpG 7909 adjuvant binds to the Toll-like receptor 9 to enhance the immune response to coadministered antigens (primarily B. anthracis protective antigen) (7,8). The PEP schedule, under clinical evaluation for AV7909, is 0.5 mL AVA with 0.25 mg CpG 7909 adjuvant administered IM at 0 and 2 weeks postexposure, combined with antimicrobials.
Since the publication in 2010 of the Advisory Committee on Immunization Practices (ACIP) recommendations for use of anthrax vaccine in the United States (9), published studies have 1) addressed the efficacy, immunogenicity, and reactogenicity of the recommended and alternate dose-sparing schedules of AVA; 2) estimated AVA efficacy in humans from data on animal efficacy and human antibody levels by using a correlates of protection model; and 3) evaluated whether developing chronic illnesses or having adverse pregnancy outcomes are associated with previous AVA receipt. In addition, AV7909 phase 1 and 2 clinical trials have demonstrated the potential of AV7909 for use as the vaccine component of PEP (PEP-Vx) (10–12).
Given these newly available data, CDC asked ACIP to revise the recommendations for use of anthrax vaccines in the United States. These revised recommendations address the IM versus SC administration of AVA for PEP and the use of reduced-schedule and half-dose AVA during public health emergencies, shortening the duration of antimicrobials given in conjunction with PEP-Vx, and extending the AVA PrEP booster dose interval after the initial priming and booster series. This report provides recommendations and guidance regarding the use of AVA for PrEP and PEP and updates the ACIP anthrax vaccination recommendations published in 2002 and 2010. This report also describes available data for AV7909 because of its potential for prelicensure emergency use during a large-scale anthrax public health emergency if the AVA supply is inadequate. This report can be used by health care providers to update the current practice for providing anthrax vaccine for PrEP and PEP and can be used by emergency preparedness partners to develop emergency vaccine response plans in preparation for a wide-area aerosolized release of B. anthracis spores.
During March 2017–January 2019, the ACIP Anthrax Vaccines Work Group (AVWG), which comprises professionals from academic medicine (internal medicine, pediatrics, obstetrics, and infectious disease specialists), federal and state public health entities, and medical societies, participated in monthly telephone conferences facilitated by CDC. During these meetings, AVWG reviewed relevant scientific evidence and evaluated the quality of the evidence assessing the 1) immunogenicity and safety of an extended booster dose interval for PrEP in persons not at high risk for exposure to B. anthracis but who might have a future high risk for exposure; 2) benefits and harms of the IM versus SC route of administration for PEP-Vx; 3) benefits and harms of AVA dose-sparing schedules (i.e., 2 full doses or 3 half doses) for PEP-Vx if vaccination demands were to exceed vaccine supply after a wide-area aerosolized release of B. anthracis spores; 4) immunogenicity and safety of AV7909, based on available data; and 5) use of anthrax antitoxin for PEP in conjunction with anthrax vaccine.
A scientific literature search was conducted through a systematic review for studies involving human subjects or for animal studies that met criteria for the Animal Rule (13,14) that reported primary data on important health outcomes related to AVA or AV7909 published after 2008. The previous ACIP review summarized the data through 2008 (9). Databases searched in February 2017 included Medline (OVID), Embase (OVID), CAB Abstracts (OVID), Global Health (OVID), CINAHL (Ebsco), Econlit (Ebsco), Cochrane Library, Clinical Trials.gov, FedRip (Ebsco), the U.S. Department of Defense (DoD) Technical Information Center, NTIS:NTRL, Scopus, WHOLIS, and WorldCat. Search terms included anthrax vaccine, AVA, Biothrax, Nuthrax, AV7909, CpG DNA, CpG 7909, CpG motifs, CpG oligodeoxynucleotide, Anthim, Anthrasil, obiltoxaximab, and raxibacumab. In addition, the work group reviewed unpublished data from the CDC Anthrax Vaccine Research Program, unpublished data from the vaccine manufacturer, and results of studies from the Vaccine Analytic Unit, which is a CDC-led collaboration with DoD and FDA that assessed potential associations of AVA with development of chronic conditions (15). The review of vaccine safety also included adverse events reported to the Vaccine Adverse Event Reporting System (VAERS) after AVA administration for January 1, 2009, through June 30, 2017 (16). To qualify as a candidate for inclusion in the review, a study had to present immunogenicity or safety data on AVA, AV7909, or infectious disease vaccines that used CpG 7909 adjuvant. Studies were excluded if they lacked mention of either AVA or AV7909 for the prevention of anthrax, lacked primary data, or were outside the time frame of interest.
Data were abstracted and summarized for immunogenicity outcomes of interest, including seroconversion, geometric mean concentration (GMC) of anti-protective antigen immunoglobulin G (anti-PA IgG, determined by enzyme-linked immunosorbent assay), geometric mean titer (GMT) of toxin neutralization activity (TNA), effective dose 50 (ED50) levels, and GMT of TNA neutralization factor 50 (NF50) levels. Data also were abstracted and summarized for safety outcomes of interest, including injection site adverse events, systemic adverse events, and serious adverse events. Quality of evidence was evaluated and presented in tabular format using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach (17).
Evidence that had been summarized for and reviewed by AVWG was publicly presented at the ACIP meetings in June 2017, October 2017, February 2018, June 2018, October 2018, and February 2019 (18). After a public comment period, ACIP voting members at the June 2018 and February 2019 meetings unanimously approved the proposed recommendations.
Risk for Exposure to Anthrax
The risk for exposure to aerosolized B. anthracis spores in the United States is very low (19). Anthrax is only endemic in a few sparsely populated areas in the western United States (20). Certain occupations and other activities place persons at higher risk for exposure (21). These include laboratory work that involves bioproduction of large quantities, volumes, or high concentrations of B. anthracis spores and activities with a high potential for exposure to aerosolized B. anthracis spores, such as military deployment to areas designated by DoD as posing a high risk for anthrax exposure and emergency response activities after release of B. anthracis spores (9).
The possibility exists of an intentional wide-area aerosolized release of B. anthracis spores over a densely populated area in the United States. In 2001, letters containing B. anthracis spores sent through the U.S. Postal Service led to 22 cases of anthrax, five of which were fatal (22). In addition, certain countries and terrorist groups have explored the use of anthrax as a bioweapon (23–25). An aerosolized release of B. anthracis spores over densely populated areas could become a mass-casualty incident (26). However, previously developed, publicly available clinical recommendations only addressed clinical management using conventional standards of care (27). To prepare for the possibility of an anthrax mass-casualty incident, when the number of patients is likely to exceed the ability of the health care infrastructure to provide conventional standards of care and supplies might not meet demand, the U.S. government has stockpiled equipment and therapeutics (i.e., medical countermeasures) for anthrax prevention and treatment and provided recommendations for their use (28). The U.S. government’s Strategic National Stockpile stores anthrax vaccine to be used with antimicrobials for PEP of persons with known or potential exposure to B. anthracis spores, as well as therapeutics and supplies for anthrax treatment. Animal models have shown that although 5–30 days of antimicrobials might be insufficient to prevent anthrax after single exposures or reexposures to B. anthracis spores, the addition of vaccine substantially enhances efficacy (29–31). In the event of a large-scale release of B. anthracis spores, the Strategic National Stockpile will distribute medical countermeasures to affected states, and state and local public health agencies will then dispense antimicrobials to and vaccinate numerous at-risk persons. Antimicrobials are given long enough (up to 60 days) to prevent infection until the vaccine can elicit a protective immune response (29).
Summary of Key Findings
Anthrax Vaccine Adsorbed
Because human efficacy studies of inhalation anthrax are unethical, the effectiveness of AVA for PEP cannot be directly assessed in humans. For this situation, FDA allows the use of the Animal Rule, a set of regulations that allow approval of products critical for the protection of public health and national security based on efficacy data only in animals combined with immunogenicity and safety data in animals and humans (32). Under the Animal Rule, AVA vaccine-induced antibody levels were extrapolated from vaccine efficacy studies conducted in animals to predict vaccine effectiveness in humans (33). Statistical modeling was used to establish the relation between survival of AVA-vaccinated animals challenged with B. anthracis spores and their antibody levels at the time of infectious challenge. This relation was applied to postvaccination antibody levels in humans to estimate the probability of human survival at selected time points (34).
Route of Administration and Immunogenicity of AVA for PEP
The SC route of administration of AVA is preferred in adults because SC administration results in higher antibody concentrations by week 4 than the IM route: males SC, 40.8 μg/mL (95% confidence interval [CI]: 34.0–49.1); males IM, 26.3 μg/mL (95% CI: 21.9–31.2); females SC, 60.2 μg/mL, (95% CI: 50.1–72.3), females IM, 36.0 μg/ml (95% CI: 30.0–43.1 (35). Using these antibody concentrations, survival estimates based on the correlates of protection model are 3.8% higher for the SC route (92.4%) than the IM route (88.6%) of administration at week 4 (36). However, by week 9, the antibody concentrations and predicted survival from the IM route (95.6%) and SC route (96.1%) are no longer significantly different (35).
In a wide-area aerosolized release of B. anthracis spores over a densely populated area, potentially hundreds of thousands of exposed persons might require PEP-Vx to prevent inhalation anthrax. In such a situation, rapid and efficient administration of vaccine to large numbers of persons would be a key component of the public health emergency response. Health care providers typically have more experience administering vaccines by the IM route than the SC route. In addition, during a conference call with state and local jurisdictions, many public health officials indicated that they plan to use just-in-time training for responding vaccinators during a wide-area aerosolized release of B. anthracis spores. Officials also stated during this call that training vaccinators to use the IM route was the easiest (State and local public health preparedness officials, personal communication, 2018). In addition, a study comparing the IM and SC route for AVA administration found significantly less reactogenicity (less injection site warmth, itching, erythema, induration, swelling, and nodule formation) with the IM route than with the SC route at 0, 2, and 4 weeks. In this same study, only two adverse events were more common among IM AVA recipients than SC AVA recipients: limitation of arm motion and generalized myalgia (35). Because the preponderance of injection site adverse events was associated with the SC route, concern has been raised that using this route might decrease the likelihood of patients completing the second and third doses of AVA.
Dose-Sparing Strategies for PEP-Vx
A wide-area aerosolized release of B. anthracis spores over a densely populated area could potentially require PEP-Vx of more persons than could be vaccinated with the available supply of AVA in the Strategic National Stockpile if AVA were to be administered according to the licensed regimen (0.5 mL at 0, 2, and 4 weeks) for the PEP-Vx indication. If demand were to exceed the supply, alternative AVA dose-sparing regimens might be needed to provide PEP-Vx to all persons with suspected or known exposure to aerosolized B. anthracis spores. To address this problem, studies were reviewed that estimated survival with AVA administered according to the licensed PEP-Vx schedule (3 full [0.5-ml] doses at 0, 2, and 4 weeks) versus alternate dose-sparing schedules (i.e., 2 full doses at 0 and 2 weeks, 2 full doses at 0 and 4 weeks, and 3 half [0.25-ml] doses at 0, 2, and 4 weeks) (Figure). The three groups who received an AVA dose at week 2 had higher antibody concentrations at week 4 than the one group who did not. The dose-sparing schedule of 2 full doses administered 4 weeks apart produced the highest antibody concentrations from week 6 onward after the first dose. The 3 full-dose regimen produced higher antibody concentrations than when the vaccine was administered as 3 half doses at all measured time points after week 1. The peak response was measured 2 weeks after the last dose for the licensed and dose-sparing PEP-Vx schedules and was estimated to be highly protective by the correlates of protection model (37). The predicted survival was estimated to be 97.4% (95% CI: 85.1–100) for the licensed schedule, 95.8% (95% CI: 92.2–100) for the full dose administered at 0 and 2 weeks, 98.1% (95% CI: 86.9–100) for the full dose administered at 0 and 4 weeks, and 96.1% (95% CI: 83.7–100) for the 3 half doses administered at 0, 2, and 4 weeks (Table 1). All dosing PEP-Vx schedules maintain a high level of predicted survival through week 9 (36,38).
Duration of Antimicrobial Administration in Combination with Vaccine
Since 2000, FDA has approved several oral antimicrobials (ciprofloxacin in 2000, penicillin G in 2001, doxycycline in 2001, and levofloxacin in 2004) for antimicrobial postexposure prophylaxis (PEP-Abx) of anthrax. Each PEP-Abx regimen should be administered for 60 days when not used in combination with vaccine. However, studies of nonhuman primates have demonstrated that spores can persist in the lungs many days after inhalation exposure (up to 100 days in one animal study) and that anthrax can develop after discontinuation of PEP-Abx (29,30). Because of the possibility of delayed infection from persistent spores, recommendations for PEP require use of AVA in conjunction with antimicrobial drugs. With this strategy, the antimicrobials protect against germinating spores until the vaccine can elicit a protective immune response.
Using the limited data available at the time, in 2015, FDA licensed a 3-dose regimen of AVA to be given in conjunction with recommended antimicrobials for PEP for persons potentially exposed to aerosolized B. anthracis spores (39). Newer data from a human clinical trial with AVA demonstrate that, with concurrent receipt of AVA, the duration of antimicrobial use can be shortened from the recommended 60 days (38). In the trial, persons were given one of four PEP-Vx regimens: the licensed 3-dose schedule, a dose-sparing schedule with 2 full doses at 0 and 2 weeks, a dose-sparing schedule with 2 full doses at 0 and 4 weeks, or a dose-sparing schedule with 3 half doses at 0, 2, and 4 weeks. Antibody levels predicted to be protective in humans were extrapolated from a matched nonhuman primate nonclinical trial in which 48 nonhuman primates were given 2 doses of AVA at 0 and 2 weeks and challenged with a 200 LD50 dose of B. anthracis spores at week 4. Protection provided by anti-PA IgG was modeled using logistic regression of the measured prechallenge antibody levels at week 4 in nonhuman primates versus survival of challenge (36). The nonhuman primate prediction curve was then applied to the human antibody levels to predict protection in humans (38). The estimated peak protection both for licensed and dose-sparing AVA PEP-Vx regimens occurred 2 weeks after the last AVA dose was given. All regimens are estimated to be highly protective; protection is maintained through day 60, when the antimicrobial component of PEP is recommended to end (Table 1).
Since 2008, the vast majority of AVA vaccinations (approximately 8 million doses administered to approximately 1.9 million persons) have been administered by DoD as PrEP to its service members. The PrEP route of administration was SC until FDA approved changing the PrEP route of administration to IM in December 2008. As defined by the U.S. Code of Federal Regulations, an event is classified as serious if one or more of the following conditions is reported: death, a life-threatening illness, hospitalization or prolongation of existing hospitalization, permanent disability, or a congenital anomaly or birth defect (40). From January 1, 2009, through June 30, 2017, a total of 2,439 AVA-related adverse events were reported to VAERS (16); 329 (13.5%) of these were considered serious.
During the same period, the 10 most common reported adverse events were coded as headache (14.7%), injection site erythema (13.6%), pain (12.6%), fever (11.6%), fatigue (11.5%), arthralgia (11.2%), erythema (11.2%), injection site pain (9.9%), injection site swelling (9.8%), and rash (9.4%) on the basis of coding terms from the Medical Dictionary for Regulatory Activities. VAERS has numerous strengths, such as broad national scope and early detection of possible new, rare, or unusual patterns of adverse events. However, VAERS is a spontaneous reporting system that has important limitations, including underreporting, inconsistent data quality and report completeness, and lack of an unexposed comparison group. Therefore, the data generally cannot be used to assess whether a vaccine caused an adverse event (16).
Nine studies, including clinical vaccine trials and observational studies (10,12,35,37,41–45), also assessed serious adverse events after administration of AVA, AV7909, or both in human subjects. Serious adverse events were reported in three studies (12,35,43); however, only in the Anthrax Vaccine Review Program study (35) were the serious adverse events considered possibly related to AVA. In this study, 231 adverse events were identified in recipients of approximately 8,300 doses of AVA. Six serious adverse events, none of which was fatal, were considered to be possibly related to the vaccine, including ductal carcinoma of the breast, generalized allergic reaction, new onset bilateral arthralgia of the metacarpal joints associated with positive antinuclear antibody (ANA), bilateral pseudotumor cerebri, supraspinatous tendon tear, and new onset of generalized seizures associated with aqueductal stenosis (35).
In studies from the Vaccine Analytic Unit and other groups published since 2010, no association was found between AVA receipt and the following chronic health conditions: reduction in health-related quality of life measures (46), multisystem illness (47), long-term disabilities (48,49), type 1 diabetes (50), atrial fibrillation (51), and diffuse connective tissue diseases (52). In one case-control study, an association was identified between AVA receipt and new-onset rheumatoid arthritis if a look-back period of 3 months was used (odds ratio [OR]: 3.93; 95% CI: 1.08–14.27). However, no association between AVA and rheumatoid arthritis was identified if a longer look-back period of 3 years was used (OR: 1.03; 95% CI: 0.48–2.19) (52), suggesting that AVA exposure might trigger onset of rheumatoid arthritis in persons who would eventually have developed rheumatoid arthritis later in life.
Although AVA is not intended for use during pregnancy, DoD maintains a registry of women inadvertently vaccinated while pregnant. Studies of adverse outcomes and a cohort study of birth defects using this registry did not detect any increased rates of adverse fetal or infant outcomes among women who received AVA during their first trimester compared with receipt at other time points or no receipt of AVA (53,54). Finally, because no safety data are available for AVA use in adolescents, a presidential ethics commission proposed comparing AVA safety data for the group aged 18–20 years (the youngest group) and the group aged 21–29 years. If no significant safety difference could be found between the two age groups, then evaluations could proceed in successively younger adolescents. In a study following these suggested methods, AVA was deemed safe in adults aged 18–20 years (44); no additional studies have been conducted in younger age groups. AVWG reviewed the VAERS reports and the published literature and presented their findings to the ACIP committee. On the basis of these data, the committee concluded that no clinically significant safety concerns have been identified related to receipt of AVA since 2010 (9).
AV7909 is an investigational second-generation anthrax vaccine that is under development for PEP of inhalation anthrax in conjunction with appropriate antimicrobials. AV7909 consists of the licensed AVA combined with a novel adjuvant, CpG 7909, a synthetic immunostimulatory oligodeoxynucleotide. CpG 7909 is a Toll-like receptor 9 agonist that has been demonstrated to augment Th1 responses in humans and enhance innate and adaptive immunity (7,8)
AV7909 is intended to be added to the Strategic National Stockpile. CDC has submitted a pre–Emergency Use Authorization (EUA) request to FDA to allow potential emergency use of AV7909, in conjunction with appropriate PEP-Abx, for PEP of inhalation anthrax when the supply of the currently licensed AVA is inadequate. EUA is an authority given to the FDA commissioner to legally permit the use of an unapproved medical product or unapproved use of an approved medical product (55). Under the proposed EUA, AV7909 would be administered by the IM route as a 2-dose series 2 weeks apart in conjunction with PEP-Abx for adults aged 18–65 years. Pregnant or nursing mothers, older adults (aged ≥66 years), and children (aged <18 years) should receive AVA until data to adequately support AV7909 use in these additional populations under EUA become available.
Available data indicate that AV7909 might provide the following advantages over AVA:
Two IM doses of AV7909 administered 2 weeks apart might provide protective immunity 1–2 weeks sooner than the licensed 3-dose PEP-Vx regimen of AVA.
Compared with the licensed 3-dose AVA PEP-Vx schedule, the 2-dose schedule of AV7909 PEP provides an operational advantage in a large-scale, mass vaccination response.
Adherence might be better because more persons are likely to complete the 2-dose AV7909 PEP series than the 3-dose AVA PEP series.
The initial phase 1 clinical trial assessed immunogenicity of AVA alone and AVA plus CpG 7909 in 69 healthy adults aged 18–45 years (12). Vaccinations were administered IM on weeks 0, 2 (±1 day), and 4 (±2 days). The CpG group received AVA plus 1 mg of CpG 7909. The results showed that the peak GMT of TNA for the AV7909 group was 8.8-fold higher than that observed for the AVA-alone group; antibody peaked at week 6 in both arms. By week 3, GMT in the CpG group exceeded the peak GMT in the AVA group (reached at week 6). The TNA results paralleled those observed with anti-PA IgG, and in both assays the differences between AVA and AV7909 were statistically significant. Analysis of the phase 2 TNA threshold of protection data for AV7909 revealed that addition of the CpG 7909 adjuvant to AVA improved the kinetics and magnitude of the immune response (56). A 2-dose AV7909 regimen with 0.25 mg of CpG 7909 administered IM resulted in a similar serological response at week 9 compared with a 3-dose AVA regimen administered IM and achieved a peak response by week 4 versus week 6 for AVA.
Adverse events were assessed in three clinical trials available at the time of this review, including a total of 241 subjects who were administered at least 1 dose of AVA plus CpG 7909 in varying dose combinations (10,12,45). The most common adverse events, reported in ≥20% of persons receiving AV7909 across these clinical trials, were injection site reactions (e.g., mild to moderate pain, tenderness, and arm motion limitation); these typically resolved within 48 hours of administration. Systemic reactogenicity manifested primarily as mild to moderate fatigue, muscle ache, and headache. No deaths or serious adverse events assessed as being causally associated have been reported in AV7909 clinical studies.
In healthy adults aged 18–50 years who received CpG 7909-adjuvanted experimental vaccines for malaria and hepatitis B in the 0.25-mg dose that is combined with AVA in AV7909 (57,58), local and systemic reactions were similar to those observed in the groups who received malaria and hepatitis B vaccines without CpG 7909, and the proportion of subjects who dropped out because of adverse events did not differ between treatment and control groups (58). Reasons for discontinuation included rash, positive ANA, generalized pruritus, urticaria, and fever. These clinical trial reports suggested that these adverse events might be a result of activation of proinflammatory innate immune responses at the injection site. Theoretically, CpG 7909 could trigger the onset of autoimmune disease, possibly as a result of nonspecific T or B lymphocyte activation. Some studies reported mild to moderate increases in anti–double-stranded DNA antibody, rheumatoid factor, or positive ANA results. However, these increases in immune markers were typically transient. No adverse events suggesting autoimmune disease have been reported in the reviewed published data on CpG 7909-adjuvanted infectious disease vaccine trials (57–61). No safety data are available for CpG 7909-adjuvanted vaccines, including AV7909 among special populations (e.g., children, persons aged >65 years, and pregnant women).
Recommendations for Prevention of Anthrax Among Persons with Potential Risk for Exposure: PrEP
ACIP previously recommended AVA PrEP for prevention of anthrax in persons at high risk for exposure to B. anthracis (e.g., members of the U.S. military deployed to areas designated by DoD as high risk for exposure, laboratory workers who work with high concentrations of B. anthracis, and persons such as farmers, veterinarians, and livestock handlers who might handle infected animals or contaminated animal products) (9). In this report, ACIP recommends that a booster dose of AVA PrEP be given every 3 years to persons who are not at high risk for exposure to B. anthracis who have previously completed the 3-dose primary and the initial 2-dose boosters AVA series and want to maintain protection.
The PrEP schedule for persons at high risk for exposure to B. anthracis is AVA administered IM as a priming series at 0, 1, and 6 months, with booster doses at 12 and 18 months and annually thereafter. If the vaccination schedule is interrupted, the series does not need to be restarted. After the priming series is completed, persons can work in high-risk areas of exposure with appropriate personal protective equipment and biosafety measures. Documentation of seroconversion is not required. If biosafety or respiratory protection measures are breached and exposure to aerosolized B. anthracis spores might have occurred, a 30-day course of PEP-Abx is recommended, regardless of whether PrEP has been fully or partially completed.
Because of the lack of a quantifiable risk, emergency and other responders are not recommended to receive routine PrEP vaccination. However, emergency responders, because of the requirements of their occupation, might be exposed to aerosolized B. anthracis spores and thus may opt to receive the vaccine on a voluntary basis. For persons who are not currently at high risk for exposure to B. anthracis but who might be at high risk in the future (e.g., persons involved in emergency response activities), published data (35) support a booster dose interval of >1 year. Thus, a booster dose of AVA can be given every 3 years to persons not at high risk for exposure to B. anthracis who have previously received the initial AVA priming and booster series and who want to maintain protection. After completing the initial 3-dose priming and booster series, persons who have not received a booster dose in the last 12 months and need to enter an area where B. anthracis is suspected to be present in the environment or be in use should be given an IM booster dose and then either wait 2 weeks to enter the high-risk area or, if required to enter immediately, take PEP-Abx for 2 weeks. While in a high-risk area, a booster dose should be given within 1 year of the last booster dose.
Persons who are exposed to aerosolized B. anthracis spores but have not completed the initial priming and booster series for AVA should receive additional AVA doses and PEP-Abx. The number of vaccine doses and duration of PEP-Abx will vary in a manner commensurate with the number of previously received doses (Table 2).
Recommendations for Prevention of Anthrax Among Persons with Suspected or Known Exposure: PEP
ACIP recommends AVA for use in adults aged 18–65 years to be given in conjunction with a course of antimicrobials (Table 3) to prevent infection after suspected or known exposure to aerosolized B. anthracis spores. Antimicrobial duration details are provided (Table 4). The vaccine is given at a dose of 0.5 mL SC at 0, 2, and 4 weeks postexposure, unless the emergency response requires a change to the IM route or use of dose-sparing regimens. If the PEP-Vx schedule is interrupted, the series does not need to be restarted. Instead, subsequent doses should be administered as soon as possible, and the series should be finished.
Route of Administration
ACIP recommends the SC route of administration rather than the IM route for PEP because higher antibody concentrations are achieved by 4 weeks after AVA vaccination. However, during a large-scale emergency response, AVA for PEP can be administered using an IM route if the SC route of administration poses significant materiel, personnel, or clinical challenges that might delay or preclude vaccination. In addition, persons who experienced adverse events from AVA that was administered SC may elect to receive subsequent vaccine doses IM after consultation with a health care provider. Doses of AVA inadvertently administered by the IM route rather than the SC route do not need to be repeated by the SC route.
Dose-Sparing PEP Regimens
ACIP recommends use of dose-sparing PEP regimens if the anthrax vaccine supply is insufficient to vaccinate all potentially exposed persons. The 2 full-dose strategy will expand the existing vaccine supply by 50%, and the 3 half-dose strategy will expand the supply by 100%. Immediately after a wide-area aerosolized release of B. anthracis spores, the preferred dose-sparing PEP regimen might not be apparent until the size of the event is determined. All dose-sparing PEP-Vx regimens are estimated to provide high levels of protection 2 weeks after the last dose (Table 5). Existing data indicated that 2 doses administered 2 weeks apart or 4 weeks apart are effective; therefore, the 2-dose schedule should be ≥2 weeks apart and ≤4 weeks apart, recognizing that full protection is not achieved until 2 weeks after the second dose (37).
Antimicrobial Duration in Conjunction with FDA-Licensed or Dose-Sparing PEP Regimens of AVA
ACIP recommends that in immunocompetent adults (e.g., healthy, nonpregnant adults aged 18–65 years), PEP-Abx both for the licensed and dose-sparing PEP-Vx regimens can be discontinued 42 days after initiation of vaccine if AVA is administered on schedule for both the licensed and dose-sparing PEP-Vx regimens (Table 4). If the AVA series cannot be completed, then antimicrobial therapy should continue for 60 days. However, the second dose of AVA is critical for producing high antibody concentrations. To account for delays in initial vaccination that might occur because of the emergency situation, antimicrobial administration should be initiated as soon as possible and continued for 42 days after the first dose or 2 weeks after the last dose of the vaccine series, whichever comes last. No data on humans are available to suggest that PEP-Abx should be given for >60 days, which is the recommended duration for PEP-Abx when given without vaccine. Thus, PEP-Abx should not be given for >60 days, regardless of the timing of last vaccine dose.
The shortening of PEP-Abx duration from 60 days to 42 days, or 2 weeks after the last dose of vaccine, applies to healthy adults aged 18–65 years. Persons with immunocompromising conditions that might interfere with their ability to develop an adequate immune response or populations for whom data on immune response to AVA are lacking (e.g., children, pregnant women, and adults aged ≥65 years) should continue to receive PEP-Abx for 60 days concurrently with AVA.
Potential Emergency Use of AV7909
Because of supply concerns and the investigational status of AV7909, AVA should be prioritized over AV7909 for PEP-Vx of potential exposure to aerosolized B. anthracis spores. However, the limited amount of phase 2 safety and immunogenicity data indicate that AV7909 appears to be safe and effective. The benefits of an effective vaccine that can prevent anthrax outweigh the known potential risks for adverse events in persons potentially exposed to aerosolized B. anthracis spores. Therefore, if supplies of AVA are exhausted or unavailable, AV7909 is an option for PEP of persons exposed to aerosolized B. anthracis spores under an EUA granted by FDA. As with AVA, antimicrobials (Tables 3 and 4) should be taken in conjunction with AV7909. Additional AV7909 data on safety, immunogenicity, and biocompatibility with antimicrobials will be reviewed by ACIP as they become available, and recommendations on potential preferential use will be updated as needed.
No data are available on the immunogenicity or safety of AV7909 for children or other special populations. However, a phase 2 clinical trial is being conducted to assess the safety and immunogenicity of AVA and AV7909 in adults aged >65 years compared with adults aged 18–50 years (62). In the absence of such data, AVWG considered it reasonable to anticipate that risks and benefits of PEP-Vx for children or special populations would be similar to those for the general adult population. Therefore, if AVA is not available, emergency use of AV7909 under an appropriate regulatory mechanism should be considered for all populations with known or potential exposure to aerosolized B. anthracis spores. Should an anthrax exposure event occur that necessitates AV7909 use while it remains under development and is not yet licensed, ACIP will convene an emergency meeting to review available data for specific recommendations on AV7909 emergency use.
No studies have been conducted on the interchangeability of AVA and AV7909. When feasible, doses of the same vaccine type should be used to complete a series. However, vaccination should not be deferred because the previously used vaccine type is unavailable. When a vaccine series uses a combination of AVA and AV7909, 3 total doses of anthrax vaccine should be administered and used in conjunction with appropriate antimicrobials (Tables 3 and 5).
Antitoxin Use for PEP
Three licensed anthrax antitoxins are available from the Strategic National Stockpile: anthrax immune globulin intravenous (AIGIV) (63), obiltoxaximab (Anthim) (64), and raxibacumab (ABthrax) (65). AIGIV is a polyclonal antibody, whereas obiltoxaximab and raxibacumab are both monoclonal antibodies. All work by binding to protective antigen, which blocks movement of toxins into cells and therefore the effects of toxins within the cells. All three antitoxins are indicated in all adults and children for the treatment of inhalation anthrax due to B. anthracis, in combination with appropriate antimicrobial drugs.
Obiltoxaximab and raxibacumab also have an indication for PEP of inhalation anthrax due to B. anthracis when alternative therapies are not available or are not appropriate. In these situations, obiltoxaximab or raxibacumab may be considered to help prevent inhalation anthrax. The predicted effectiveness of both antitoxins for this indication is based solely on efficacy studies conducted in animal models of inhalation anthrax (66,67).
Data indicate that raxibacumab can be coadministered with AVA for PEP without affecting vaccine immunogenicity (68). No data are available to assess whether obiltoxaximab coadministered with AVA impairs vaccine immunogenicity. AIGIV does not have a PEP indication because coadministration of AIGIV and AVA in a rabbit model has been shown to significantly reduce the development of an immune response to AVA (68).
Vaccine Adverse Events Reporting and Additional Information
Surveillance for serious adverse events is important for all antimicrobials, biologics, and vaccines. All clinically significant adverse events after receipt of antimicrobials or anthrax antitoxin for PEP or treatment of anthrax should be reported to the MedWatch Program (https://www.fda.gov/safety/medwatch-fda-safety-information-and-adverse-event-reporting-programexternal icon or 888-463-6332). All clinically significant adverse events after receipt of either AVA or AV7909 should be reported to VAERS (https://vaers.hhs.govexternal icon or 800–822–7967). Additional information about anthrax and anthrax vaccines is available at https://www.cdc.gov/anthrax.
Research priorities for future studies on anthrax vaccines should include assessment of immunogenicity and safety in special populations, such as children, older adults, and pregnant and nursing mothers; additional evaluations of the dose-sparing schedules; evaluation of the interchangeability of AVA and AV7909; determination of the optimal booster schedule to provide long-term protection after receiving the PEP vaccine schedule; testing of the stability of AVA and AV7909 outside the cold chain; assessment of whether coadministration of obiltoxaximab with AVA impairs vaccine immunogenicity; and the optimal duration of antimicrobial use in postexposure settings. Studies are planned to evaluate the effect of longer intervals between PrEP boosters on vaccine responses. On approval of AV7909 as a licensed vaccine, the additional data leading to the licensure of AV7909 will be reviewed by ACIP, and recommendations will be updated as needed.
Marissa Persons, Modupe Osinubi, Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, CDC; Amanda Cohn, Jessica MacNeil, Office of the Director, National Center for Immunization and Respiratory Diseases, CDC. Advisory Committee on Immunization Practices (ACIP) member roster for March 2017–January 2019 is available at https://www.cdc.gov/vaccines/acip/committee/members.html.
Advisory Committee on Immunization Practices
Membership as of February 27, 2019
Chair: José R. Romero, MD, University of Arkansas for Medical Sciences and Arkansas Children’s Hospital, Little Rock, Arkansas.
Executive Secretary: Amanda Cohn, MD, National Center for Immunization and Respiratory Diseases, CDC, Atlanta, Georgia.
Members: Robert L. Atmar, MD, Baylor College of Medicine, Houston, Texas; Kevin A. Ault, MD, University of Kansas Medical Center, Kansas City, Kansas; Henry Bernstein, DO, Zucker School of Medicine at Hofstra/Northwell Cohen Childrens’ Medical Center, New Hyde Park, New York; Echezona Ezeanolue, MD, University of Nevada, Las Vegas, Nevada; Sharon E. Frey, MD, Saint Louis University Medical School, Saint Louis, Missouri; Stefan Gravenstein, MD, Providence Veterans Administration Hospital, Providence, Rhode Island; Paul Hunter, MD, City of Milwaukee Health Department, Milwaukee, Wisconsin; Grace M. Lee, MD, Lucile Packard Children’s Hospital, Stanford University School of Medicine, Stanford, California; Veronica V. McNally, JD, Fanny Strong Foundation, West Bloomfield, Michigan; Kelly Moore, MD, Vanderbilt University School of Medicine, Nashville, Tennessee; José R. Romero, MD, University of Arkansas for Medical Sciences and Arkansas Children’s Hospital, Little Rock, Arkansas; David Stephens, MD, Emory University School of Medicine, Atlanta, Georgia; Peter Szilagyi, MD, University of California, Los Angeles (UCLA), Los Angeles, California; Helen Keipp Talbot, MD, Vanderbilt University, Nashville, Tennessee; Emmanuel Walter, Jr., MD, Duke University School of Medicine, Durham, North Carolina.
Ex Officio Members: Mary Beth Hance, Centers for Medicare and Medicaid Services; Eric Deussing, MD, Department of Defense; Jane A. Kim, MD, Department of Veterans Affairs; Doran Fink, MD, Food and Drug Administration; Narayan Nair, MD, Health Resources and Services Administration; Thomas Weiser, MD, Indian Health Service; Tammy Beckham, National Vaccine Program Office; John Beigel, MD, National Institutes of Health.
Liaison Representatives: American Academy of Family Physicians, Pamela G. Rockwell, DO, Ann Arbor, Michigan; American Academy of Pediatrics, Yvonne Maldonado, MD, Stanford, California; American Academy of Pediatrics, David Kimberlin, MD, Birmingham, Alabama; American Academy of Physician Assistants, Marie-Michèle Léger, MPH, Alexandria, Virginia; American College Health Association, Susan Even, MD, Columbia, Missouri; American College of Nurse Midwives, Carol E. Hayes, MN, Atlanta, Georgia; American College of Nurse Midwives, Pamela M. Meharry, PhD; American College of Obstetricians and Gynecologists, Linda O’Neal Eckert, MD, Seattle, Washington; American College of Physicians, Jason M. Goldman, MD, Boca Raton, Florida; American Geriatrics Society, Kenneth Schmader, MD, Durham, North Carolina; America’s Health Insurance Plans, Mark J. Netoskie, MD, Houston, Texas; American Immunization Registry Association, Rebecca Coyle, MSEd, Washington DC; American Medical Association, Sandra Adamson Fryhofer, MD, Atlanta, Georgia; American Nurses Association, Charles Rittle, MPH, Pittsburgh, Pennsylvania; American Osteopathic Association, Stanley Grogg, DO, Tulsa, Oklahoma; American Pharmacists Association, Stephan L. Foster, PharmD, Memphis, Tennessee; Association of Immunization Managers, Christine Finley, MPH, Burlington, Vermont; Association for Prevention Teaching and Research, Paul W. McKinney, MD, Louisville, Kentucky; Association of State and Territorial Health Officials, Nathaniel Smith, MD, Little Rock, Arkansas; Biotechnology Industry Organization, Phyllis A. Arthur, MBA, Washington, DC; Council of State and Territorial Epidemiologists, Christine Hahn, MD, Boise, Idaho; Canadian National Advisory Committee on Immunization, Caroline Quach, MD, Montreal, Québec, Canada; Infectious Diseases Society of America, Carol J. Baker, MD, Houston, Texas; National Association of County and City Health Officials, Matthew Zahn, MD, Santa Ana, California; National Association of County and City Health Officials, Jeffrey Duchin, MD, Seattle, Washington; National Association of Pediatric Nurse Practitioners, Patricia A. Stinchfield, MS, St. Paul, Minnesota; National Foundation for Infectious Diseases, William Schaffner, MD, Nashville, Tennessee; Mexico National Immunization Council and Child Health Program, Luis Duran, MD, Mexico; National Medical Association, Patricia Whitley-Williams, MD, New Brunswick, New Jersey; Pediatric Infectious Diseases Society, Sean O’Leary, MD, Colorado; Pediatric Infectious Diseases Society, Mark H. Sawyer, MD, San Diego, California; Pharmaceutical Research and Manufacturers of America, David R. Johnson, MD, Swiftwater, Pennsylvania; Society for Adolescent Health and Medicine, Amy B. Middleman, MD, Oklahoma City, Oklahoma; Society for Healthcare Epidemiology of America, David Weber, MD, Chapel Hill, North Carolina.
ACIP Anthrax Vaccine Work Group
ACIP Members: David S. Stephens, MD, Chair, Emory University School of Medicine, Atlanta, Georgia; Robert L. Atmar, MD, Baylor College of Medicine, Houston, Texas; Sharon E. Frey, MD, St. Louis University Medical School, St. Louis, Missouri.
Ex Officio Members: Eric Espeland, PhD, Biomedical Advanced Research and Development Authority, Washington, DC; Chia-Wei Tsai, PhD, Biomedical Advanced Research and Development Authority, Washington, DC; Amanda Zarrabian, MS, Biomedical Advanced Research and Development Authority, Washington, DC; Eric Deussing, MD, Department of Defense, Atlanta, Georgia; Alexandra Worobec, MD, Food and Drug Administration, Washington, DC; Julianne Clifford, PhD, Food and Drug Administration, Washington, DC; Judy Hewitt, PhD, National Institutes of Health, Bethesda, Maryland; Kim Taylor, PhD, National Institutes of Health, Bethesda, Maryland.
Liaison Representatives: American College of Obstetricians and Gynecologists, Richard Beigi, MD, Pittsburgh, Pennsylvania; Infectious Diseases Society of America, Kathleen Neuzil, MD, Baltimore, Maryland; American Academy of Pediatrics, James D. Campbell, MD, Golden, Colorado; National Association of County and City Health Officials, Matthew Zahn, MD, Orange, California.
Invited Consultants: Wendy Keitel, MD, Baylor College of Medicine, Houston, Texas; Arthur Friedlander, MD, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland; Phillip Pittman, MD, United States Army Medical Research Institute of Infectious Diseases, Fort Detrick, Maryland; Andy Pavia, MD, University of Utah, Salt Lake City, Utah; Stacy Hall, MSN, Louisiana Office of Public Health, New Orleans, Louisiana.
CDC Contributors: Kate Hendricks, MD, CDC, Atlanta, Georgia; Jarad Schiffer, MS, CDC, Atlanta, Georgia; Conrad Quinn, PhD, CDC, Atlanta, Georgia; Charles Rose, PhD, CDC, Atlanta, Georgia; Michael M. McNeil, MD, CDC, Atlanta, Georgia; Jennifer Wright, DVM, CDC, Atlanta, Georgia; Yon Yu, PharmD, CDC, Atlanta, Georgia; Marie de Perio, MD, CDC, Cincinnati, Ohio.
Work Group Secretariat: William Bower, MD, CDC, Atlanta, Georgia.
Corresponding author: William A. Bower, Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, CDC. Telephone: 404-639-0376; E-mail: email@example.com.
1Division of High-Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, CDC; 2Division of Bacterial Diseases, National Center for Immunization and Respiratory Diseases, CDC; 3Department of Medicine, Baylor College of Medicine, Houston, Texas; 4Department of Molecular Virology & Microbiology and Department of Medicine, Baylor College of Medicine, Houston, Texas; 5U.S. Army Medical Research Institute of Infectious Diseases, Frederick, Maryland; 6Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, CDC; 7Department of Medicine, Emory University, Atlanta, Georgia; 8Office of Laboratory Science, CDC
Conflicts of Interest
All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. No potential conflicts of interest were disclosed.
CDC Adoption of ACIP Recommendations for MMWR Recommendations and Reports, MMWR Policy Notes, and Immunization Schedules (Child/Adolescent, Adult):
Recommendations for routine use of vaccines in children, adolescents, and adults are developed by the Advisory Committee on Immunization Practices (ACIP). ACIP is chartered as a federal advisory committee to provide expert external advice and guidance to the Director of CDC on use of vaccines and related agents for the control of vaccine-preventable diseases in the civilian population of the United States. Recommendations for routine use of vaccines in children and adolescents are harmonized to the greatest extent possible with recommendations made by the American Academy of Pediatrics (AAP), the American Academy of Family Physicians (AAFP), and the American College of Obstetricians and Gynecologists (ACOG). Recommendations for routine use of vaccines in adults are harmonized with recommendations of AAFP, ACOG, and the American College of Physicians (ACP). ACIP recommendations approved by the CDC Director become agency guidelines on the date published in the Morbidity and Mortality Weekly Report (MMWR). Additional information is available at https://www.cdc.gov/vaccines/acip.
- Davies JC. A major epidemic of anthrax in Zimbabwe. The experience at the Beatrice Road Infectious Diseases Hospital, Harare. Cent Afr J Med 1985;31:176–80. PubMedexternal icon
- Holty JE, Bravata DM, Liu H, Olshen RA, McDonald KM, Owens DK. Systematic review: a century of inhalational anthrax cases from 1900 to 2005. Ann Intern Med 2006;144:270–80. CrossRefexternal icon PubMedexternal icon
- Katharios-Lanwermeyer S, Holty JE, Person M, et al. Identifying meningitis during an anthrax mass casualty incident: systematic review of systemic anthrax since 1880. Clin Infect Dis 2016;62:1537–45. CrossRefexternal icon PubMedexternal icon
- Booth MG, Hood J, Brooks TJ, Hart A; Health Protection Scotland Anthrax Clinical Network. Anthrax infection in drug users. Lancet 2010;375:1345–6. CrossRefexternal icon PubMedexternal icon
- US Department of Agriculture; CDC. Federal Select Agent Program: select agents and toxins FAQS. Washington, DC: US Department of Agriculture; Atlanta, GA: CDC. https://www.selectagents.gov/faq-general.htmlexternal icon
- US Food and Drug Administration. Full prescribing information: BioThrax (Anthrax Vaccine Adsorbed). Silver Spring, MD: US Food and Drug Administration. https://www.fda.gov/media/71954/downloadexternal icon
- Klinman DM, Xie H, Little SF, Currie D, Ivins BE. CpG oligonucleotides improve the protective immune response induced by the anthrax vaccination of rhesus macaques. Vaccine 2004;22:2881–6. CrossRefexternal icon PubMedexternal icon
- Krieg AM. Therapeutic potential of Toll-like receptor 9 activation. Nat Rev Drug Discov 2006;5:471–84. CrossRefexternal icon PubMedexternal icon
- Wright JG, Quinn CP, Shadomy S, Messonnier N. Use of anthrax vaccine in the United States: recommendations of the Advisory Committee on Immunization Practices (ACIP), 2009. MMWR Recomm Rep 2010;59(No. RR-6). PubMedexternal icon
- Hopkins RJ, Daczkowski NF, Kaptur PE, et al. Randomized, double-blind, placebo-controlled, safety and immunogenicity study of 4 formulations of anthrax vaccine adsorbed plus CPG 7909 (AV7909) in healthy adult volunteers. Vaccine 2013;31:3051–8. CrossRefexternal icon PubMedexternal icon
- Minang JT, Inglefield JR, Harris AM, et al. Enhanced early innate and T cell-mediated responses in subjects immunized with anthrax vaccine adsorbed plus CPG 7909 (AV7909). Vaccine 2014;32:6847–54. CrossRefexternal icon PubMedexternal icon
- Rynkiewicz D, Rathkopf M, Sim I, et al. Marked enhancement of the immune response to BioThrax® (anthrax vaccine adsorbed) by the TLR9 agonist CPG 7909 in healthy volunteers. Vaccine 2011;29:6313–20. CrossRefexternal icon PubMedexternal icon
- Burns DL. Licensure of vaccines using the Animal Rule. Curr Opin Virol 2012;2:353–6. CrossRefexternal icon PubMedexternal icon
- US Food and Drug Administration. Product development under the Animal Rule. Silver Spring, MD: US Food and Drug Administration. https://www.fda.gov/media/88625/downloadexternal icon.
- Payne DC, Franzke LH, Stehr-Green PA, Schwartz B, McNeil MM. Development of the Vaccine Analytic Unit’s research agenda for investigating potential adverse events associated with anthrax vaccine adsorbed. Pharmacoepidemiol Drug Saf 2007;16:46–54. CrossRefexternal icon PubMedexternal icon
- Shimabukuro TT, Nguyen M, Martin D, DeStefano F. Safety monitoring in the Vaccine Adverse Event Reporting System (VAERS). Vaccine 2015;33:4398–405. CrossRefexternal icon PubMedexternal icon
- CDC. GRADE (Grading of Recommendations, Assessment, Development and Evaluation). Atlanta, GA: US Department of Health and Human Services, CDC. https://www.cdc.gov/vaccines/acip/recs/grade
- CDC. ACIP meeting information. Atlanta, GA: US Department of Health and Human Services, CDC. https://www.cdc.gov/vaccines/acip/meetings/index.html
- Bales ME, Dannenberg AL, Brachman PS, Kaufmann AF, Klatsky PC, Ashford DA. Epidemiologic response to anthrax outbreaks: field investigations, 1950–2001. Emerg Infect Dis 2002;8:1163–74. CrossRefexternal icon PubMedexternal icon
- Blackburn JK, McNyset KM, Curtis A, Hugh-Jones ME. Modeling the geographic distribution of Bacillus anthracis, the causative agent of anthrax disease, for the contiguous United States using predictive ecological [corrected] niche modeling. Am J Trop Med Hyg 2007;77:1103–10. CrossRefexternal icon PubMedexternal icon
- Anthrax in humans. In: World Health Organization. Anthrax in humans and animals. 4th ed. Geneva, Switzerland; World Health Organization; 2008:36–52. https://www.who.int/csr/resources/publications/anthrax_webs.pdfpdf iconexternal icon
- Jernigan DB, Raghunathan PL, Bell BP, et al. ; National Anthrax Epidemiologic Investigation Team. Investigation of bioterrorism-related anthrax, United States, 2001: epidemiologic findings. Emerg Infect Dis 2002;8:1019–28. CrossRefexternal icon PubMedexternal icon
- Christopher GW, Cieslak TJ, Pavlin JA, Eitzen EM. Biological warfare: a historical perspective. JAMA 1997;278:412–7.
- Cole LA. The specter of biological weapons. Sci Am 1996;275:60–5.
- Zilinskas RA. Iraq’s biological weapons: the past as future? JAMA 1997;278:418–24.
- World Health Organization. Health aspects of chemical and biological weapons, report of a WHO group of consultants. Geneva, Switzerland; World Health Organization; 1970.
- Hendricks KA, Wright ME, Shadomy SV, et al. ; Workgroup on Anthrax Clinical Guidelines. Centers for Disease Control and Prevention expert panel meetings on prevention and treatment of anthrax in adults. Emerg Infect Dis 2014;20. CrossRefexternal icon PubMedexternal icon
- Bowere WA, Hendricks K, Pillai S, Guarnizo J, Meaney Delman D. Clinical framework and medical countermeasure use during an anthrax mass-casualty incident: CDC recommendations. MMWR Recomm Rep 2015;64(No. RR-4).
- Henderson DW, Peacock S, Belton FC. Observations on the prophylaxis of experimental pulmonary anthrax in the monkey. J Hyg (Lond) 1956;54:28–36. CrossRefexternal icon PubMedexternal icon
- Friedlander AM, Welkos SL, Pitt ML, et al. Postexposure prophylaxis against experimental inhalation anthrax. J Infect Dis 1993;167:1239–42. CrossRefexternal icon PubMedexternal icon
- Vietri NJ, Purcell BK, Lawler JV, et al. Short-course postexposure antibiotic prophylaxis combined with vaccination protects against experimental inhalational anthrax. Proc Natl Acad Sci U S A 2006;103:7813–6. CrossRefexternal icon PubMedexternal icon
- US Food and Drug Administration. Pathway to licensure for protective antigen-based anthrax vaccines for a post-exposure prophylaxis indication using the Animal Rule: briefing document for the Vaccines and Related Biological Products Advisory Committee Meeting. Silver Spring, MD: US Food and Drug Administration; November 16, 2010. http://wayback.archive-it.org/7993/20170113080506/http:/www.fda.gov/downloads/AdvisoryCommittees/CommitteesMeetingMaterials/BloodVaccinesandOtherBiologics/VaccinesandRelatedBiologicalProductsAdvisoryCommittee/UCM232400.pdfpdf iconexternal icon
- Fay MP, Follmann DA, Lynn F, et al. Anthrax vaccine-induced antibodies provide cross-species prediction of survival to aerosol challenge. Sci Transl Med 2012;4:151ra126. CrossRefexternal icon PubMedexternal icon
- Schiffer JM, Chen L, Dalton S, Niemuth NA, Sabourin CL, Quinn CP. Bridging non-human primate correlates of protection to reassess the anthrax vaccine adsorbed booster schedule in humans. Vaccine 2015;33:3709–16. CrossRefexternal icon PubMedexternal icon
- Wright JG, Plikaytis BD, Rose CE, et al. Effect of reduced dose schedules and intramuscular injection of anthrax vaccine adsorbed on immunological response and safety profile: a randomized trial. Vaccine 2014;32:1019–28. CrossRefexternal icon PubMedexternal icon
- Sivko GS, Stark GV, Tordoff KP, et al. Evaluation of early immune response-survival relationship in cynomolgus macaques after anthrax vaccine adsorbed vaccination and Bacillus anthracis spore challenge. Vaccine 2016;34:6518–28. CrossRefexternal icon PubMedexternal icon
- Bernstein DI, Jackson L, Patel SM, et al. Immunogenicity and safety of four different dosing regimens of anthrax vaccine adsorbed for post-exposure prophylaxis for anthrax in adults. Vaccine 2014;32:6284–93. CrossRefexternal icon PubMedexternal icon
- Stark GV, Sivko GS, VanRaden M, et al. Cross-species prediction of human survival probabilities for accelerated anthrax vaccine adsorbed (AVA) regimens and the potential for vaccine and antibiotic dose sparing. Vaccine 2016;34:6512–7. CrossRefexternal icon PubMedexternal icon
- US Food and Drug Administration. Summary basis for regulatory action—BioThrax (Anthrax Vaccine Adsorbed). Silver Spring, MD: US Food and Drug Administration; 2015. https://www.fda.gov/media/94823/downloadexternal icon
- US Food and Drug Administration. 21 CFR Sec. 310.305 Records and reports concerning adverse drug experiences on marketed prescription drugs for human use without approved new drug applications. Federal Register 2018;5. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/CFRSearch.cfm?fr=310.305external icon
- Zhang Y, Martin SW, Rose CE Jr, et al. Evaluation of body mass index, pre-vaccination serum progesterone levels and anti-anthrax protective antigen immunoglobulin G on injection site adverse events following anthrax vaccination in women. Pharmacoepidemiol Drug Saf 2008;17:1060–7. CrossRefexternal icon PubMedexternal icon
- Ionin B, Hopkins RJ, Pleune B, et al. Evaluation of immunogenicity and efficacy of anthrax vaccine adsorbed for postexposure prophylaxis. Clin Vaccine Immunol 2013;20:1016–26. CrossRefexternal icon PubMedexternal icon
- Hopkins RJ, Howard C, Hunter-Stitt E, et al. Phase 3 trial evaluating the immunogenicity and safety of a three-dose BioThrax® regimen for post-exposure prophylaxis in healthy adults. Vaccine 2014;32:2217–24. CrossRefexternal icon PubMedexternal icon
- King JC Jr, Gao Y, Quinn CP, Dreier TM, Vianney C, Espeland EM. Evaluation of anthrax vaccine safety in 18 to 20 year olds: a first step towards age de-escalation studies in adolescents. Vaccine 2015;33:2470–6. CrossRefexternal icon PubMedexternal icon
- Hopkins RJ, Kalsi G, Montalvo-Lugo VM, et al. Randomized, double-blind, active-controlled study evaluating the safety and immunogenicity of three vaccination schedules and two dose levels of AV7909 vaccine for anthrax post-exposure prophylaxis in healthy adults. Vaccine 2016;34:2096–105. CrossRefexternal icon PubMedexternal icon
- Stewart B, Rose CE, Tokars JI, et al. Health-related quality of life in the CDC anthrax vaccine adsorbed human clinical trial. Vaccine 2012;30:5875–9. CrossRefexternal icon PubMedexternal icon
- Phillips CJ, Matyas GR, Hansen CJ, Alving CR, Smith TC, Ryan MA. Antibodies to squalene in U.S. Navy Persian Gulf War veterans with chronic multisymptom illness. Vaccine 2009;27:3921–6. CrossRefexternal icon PubMedexternal icon
- Sulsky SI, Luippold R, Garman P, et al. Disability among U.S. Army veterans vaccinated against anthrax. Vaccine 2012;30:6150–6. CrossRefexternal icon PubMedexternal icon
- Sulsky SI, Luippold RS, Garman P, Hughes H, Amoroso PJ. Risk of disability for U.S. Army personnel vaccinated against anthrax, 1998–2005. Vaccine 2011;29:6035–41. CrossRefexternal icon PubMedexternal icon
- Duderstadt SK, Rose CE Jr, Real TM, et al. Vaccination and risk of type 1 diabetes mellitus in active component U.S. military, 2002–2008. Vaccine 2012;30:813–9. CrossRefexternal icon PubMedexternal icon
- McNeil MM, Duderstadt SK, Sabatier JF, Ma GG, Duffy J. Vaccination and risk of lone atrial fibrillation in the active component United States military. Hum Vaccin Immunother 2019;15:669–76. CrossRefexternal icon PubMedexternal icon
- Bardenheier BH, Duffy J, Duderstadt SK, et al. Anthrax vaccine and the risk of rheumatoid arthritis and systemic lupus erythematosus in the U.S. military: a case-control study. Mil Med 2016;181:1348–56. CrossRefexternal icon PubMedexternal icon
- Conlin AM, Bukowinski AT, Gumbs GR; Department of Defense Birth and Infant Health Registry Team. Analysis of pregnancy and infant health outcomes among women in the National Smallpox Vaccine in Pregnancy Registry who received anthrax vaccine adsorbed. Vaccine 2015;33:4387–90. CrossRefexternal icon PubMedexternal icon
- Conlin AMS, Sevick CJ, Gumbs GR, Khodr ZG, Bukowinski AT. Safety of inadvertent anthrax vaccination during pregnancy: an analysis of birth defects in the U.S. military population, 2003–2010. Vaccine 2017;35:4414–20. CrossRefexternal icon PubMedexternal icon
- US Food and Drug Administration. Emergency use authorization of medical products and related authorities. Silver Spring, MD: US Food and Drug Administration; 2017. https://www.fda.gov/media/97321/downloadexternal icon
- National Institutes of Health. A phase 2 safety and immunogenicity study for an anthrax vaccine using 3 schedules and two dose levels. Washington, DC: National Institutes of Health; 2015. https://clinicaltrials.gov/ct2/show/results/NCT01770743?view=resultsexternal icon
- Cooper CL, Davis HL, Morris ML, et al. CPG 7909, an immunostimulatory TLR9 agonist oligodeoxynucleotide, as adjuvant to Engerix-B HBV vaccine in healthy adults: a double-blind phase I/II study. J Clin Immunol 2004;24:693–701. CrossRefexternal icon PubMedexternal icon
- Ellis RD, Martin LB, Shaffer D, et al. Phase 1 trial of the Plasmodium falciparum blood stage vaccine MSP1(42)-C1/Alhydrogel with and without CPG 7909 in malaria naïve adults. PLoS One 2010;5:e8787. CrossRefexternal icon PubMedexternal icon
- Cooper CL, Davis HL, Morris ML, et al. Safety and immunogenicity of CPG 7909 injection as an adjuvant to Fluarix influenza vaccine. Vaccine 2004;22:3136–43. CrossRefexternal icon PubMedexternal icon
- Cooper CL, Davis HL, Angel JB, et al. CPG 7909 adjuvant improves hepatitis B virus vaccine seroprotection in antiretroviral-treated HIV-infected adults. AIDS 2005;19:1473–9. CrossRefexternal icon PubMedexternal icon
- Mullen GE, Ellis RD, Miura K, et al. Phase 1 trial of AMA1-C1/Alhydrogel plus CPG 7909: an asexual blood-stage vaccine for Plasmodium falciparum malaria. PLoS One 2008;3:e2940. CrossRefexternal icon PubMedexternal icon
- US National Library of Medicine. BARDA Securing Anthrax Immunity For the Elderly (B-SAFE) study. Bethesda, MD: US National Library of Medicine. https://clinicaltrials.gov/ct2/show/NCT03518125?cond=AV7909&draw=1&rank=3external icon
- Anthim. Package insert. Pine Brook, NJ: Elusys Therapeutics; 2016. https://www.accessdata.fda.gov/drugsatfda_docs/label/2016/125509lbl.pdfpdf iconexternal icon
- Raxibacumab. Package insert. Rockville, MD: GlaxoSmithKline; 2012. https://www.accessdata.fda.gov/drugsatfda_docs/label/2012/125349s000lbl.pdfpdf iconexternal icon
- Anthrasil. Package insert. Manitoba, Canada: Emergent BioSolutions; 2015. https://www.fda.gov/media/91577/downloadexternal icon.
- Migone TS, Subramanian GM, Zhong J, et al. Raxibacumab for the treatment of inhalational anthrax. N Engl J Med 2009;361:135–44. CrossRefexternal icon PubMedexternal icon
- Yamamoto BJ, Shadiack AM, Carpenter S, et al. Obiltoxaximab prevents disseminated Bacillus anthracis infection and improves survival during pre- and postexposure prophylaxis in animal models of inhalational anthrax. Antimicrob Agents Chemother 2016;60:5796–805. CrossRefexternal icon PubMedexternal icon
- Malkevich NV, Basu S, Rudge TL Jr, et al. Effect of anthrax immune globulin on response to BioThrax (anthrax vaccine adsorbed) in New Zealand white rabbits. Antimicrob Agents Chemother 2013;57:5693–6. CrossRefexternal icon PubMedexternal icon
FIGURE. Group geometric means for anti-protective antigen immunoglobulin G enzyme-linked immunosorbent assay over time after administration of anthrax vaccine adsorbed*
Abbreviations: AVA = anthrax vaccine adsorbed; IgG = immunoglobulin G; PA = protective antigen.
* 0, 2 Full dose = 0.5 mL AVA administered at 0 and 2 weeks; 0, 4 Full dose = 0.5 mL AVA administered at 0 and 4 weeks; 0, 2, 4 Full dose = 0.5 mL AVA administered at 0, 2, and 4 weeks; 0, 2, 4 Half dose = 0.25 mL AVA administered at 0, 2, and 4 weeks; PA80 = 80% predicted protection level.
|Dose||Route of administration||Dosing schedule|
|0.5 mL (full dose)||SC or IM*||2 doses: 0 and 2–4 wks|
|0.25 mL (half dose)||SC or IM*||3 doses: 0, 2, and 4 wks|
Suggested citation for this article: Bower WA, Schiffer J, Atmar RL, et al. Use of Anthrax Vaccine in the United States: Recommendations of the Advisory Committee on Immunization Practices, 2019. MMWR Recomm Rep 0019;68(No. RR-4):1–14. DOI: http://dx.doi.org/10.15585/mmwr.rr6804a1external icon.
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