Use of a Modified Preexposure Prophylaxis Vaccination Schedule to Prevent Human Rabies: Recommendations of the Advisory Committee on Immunization Practices — United States, 2022
Weekly / May 6, 2022 / 71(18);619–627
Please note: This report has been corrected.
Agam K. Rao, MD1; Deborah Briggs, PhD2; Susan M. Moore, PhD2; Florence Whitehill, DVM1,3; Doug Campos-Outcalt, MD4; Rebecca L. Morgan, PhD5; Ryan M. Wallace, DVM1; José R. Romero, MD6; Lynn Bahta, MPH7; Sharon E. Frey, MD8; Jesse D. Blanton, DrPH1 (View author affiliations)View suggested citation
What is already known about this topic?
Rabies is a zoonotic infection that is nearly always fatal. Preexposure prophylaxis (PrEP) is recommended for certain persons at high risk for exposure.
What is added by this report?
During 2019–2021, the Advisory Committee on Immunization Practices made multiple updates to the rabies PrEP recommendations, including the following: a 2-dose (days 0 and 7) intramuscular rabies vaccination series replaced the 3-dose schedule, a one-time titer or booster dose was advised for persons with risk for only recognized rabies exposures, risk categories were redefined, and the minimum acceptable rabies antibody titer was changed to 0.5 IU/mL.
What are the implications for public health practice?
The updates are as efficacious as previous recommendations and might facilitate improved adherence to vaccination recommendations.
Views equals page views plus PDF downloads
Human rabies is an acute, progressive encephalomyelitis that is nearly always fatal once symptoms begin. Several measures have been implemented to prevent human rabies in the United States, including vaccination of targeted domesticated and wild animals, avoidance of behaviors that might precipitate an exposure (e.g., provoking high-risk animals), awareness of the types of animal contact that require postexposure prophylaxis (PEP), and use of proper personal protective equipment when handling animals or laboratory specimens. PEP is widely available in the United States and highly effective if administered after an exposure occurs. A small subset of persons has a higher level of risk for being exposed to rabies virus than does the general U.S. population; these persons are recommended to receive preexposure prophylaxis (PrEP), a series of human rabies vaccine doses administered before an exposure occurs, in addition to PEP after an exposure. PrEP does not eliminate the need for PEP; however, it does simplify the rabies PEP schedule (i.e., eliminates the need for rabies immunoglobulin and decreases the number of vaccine doses required for PEP). As rabies epidemiology has evolved and vaccine safety and efficacy have improved, Advisory Committee on Immunization Practices (ACIP) recommendations to prevent human rabies have changed. During September 2019–November 2021, the ACIP Rabies Work Group considered updates to the 2008 ACIP recommendations by evaluating newly published data, reviewing frequently asked questions, and identifying barriers to adherence to previous ACIP rabies vaccination recommendations. Topics were presented and discussed during six ACIP meetings. The following modifications to PrEP are summarized in this report: 1) redefined risk categories; 2) fewer vaccine doses in the primary vaccination schedule; 3) flexible options for ensuring long-term protection, or immunogenicity; 4) less frequent or no antibody titer checks for some risk groups; 5) a new minimum rabies antibody titer (0.5 international units [IUs]) per mL); and 6) clinical guidance, including for ensuring effective vaccination of certain special populations.
Transmission of rabies virus occurs when saliva or neural tissue from an infected mammal is introduced into a person or another animal through, for example, a bite or contact with mucous membranes (1). Worldwide, approximately 59,000 human rabies deaths occur each year (2). The canine rabies virus variant (CRVV) is the most common source of human rabies infections, accounting for approximately 98% of cases, including some cases among U.S. travelers (3). In the United States, CRVV has been eliminated (3), but wildlife rabies remains endemic, accounting for approximately 5,000 reported rabid animals each year (4). Specific wildlife rabies virus variants (RVVs) associated with mesocarnivores (small to midsized animals whose diet includes 50%–70% meat) are endemic in distinct geographically confined locations in 42 U.S. states and Puerto Rico (4). In contrast, bat RVVs are widely distributed throughout the United States, with only Hawaii being rabies-free (3). During January 2000–December 2020, 52 cases of human rabies were diagnosed in the United States, 38 of which were indigenously acquired (i.e., from rabies exposures that occurred in the United States) (4); none were in persons who had previously received PrEP.
In the United States, two modern cell culture vaccines are licensed for rabies PrEP and PEP: human diploid cell vaccine (HDCV; Imovax/Sanofi Pasteur)* and purified chick embryo cell vaccine (PCECV; RabAvert/Bavarian Nordic),† respectively; both are packaged for intramuscular (IM) administration (1). Each IM dose of vaccine consists of 1 mL and should be administered in the deltoid for adults, and in either the deltoid or anterolateral aspect of the thigh for children.
ACIP has recommended rabies PrEP since 1969 (5). As safe and effective modern cell culture vaccines have replaced those derived from nerve tissue and duck embryo, and as rabies epidemiology has continued to evolve (e.g., elimination of CRVV, emergence and spread of the racoon RVV, and host shifts of bat RVV to mesocarnivores in the southern United States), changes have been made to ACIP recommendations. Since 2008, when the last ACIP rabies PrEP recommendations were published, barriers affecting adherence to the recommendations have been identified, including out-of-pocket costs of rabies biologics (3-dose PrEP vaccination series is currently estimated at ≥$1,100§), confusion about which activities fall within different risk categories, and noncompliance with recommendations for repeated titer checks (6). In addition, travel medicine providers have indicated that the largest group for which PrEP is recommended (travelers to regions with endemic CRVV) might often be unable to complete the 3-dose series described in the 2008 ACIP recommendations (1) because at least 21 days are required to complete the series before initiation of travel (7).
During September 2019–November 2021, the ACIP Rabies Work Group participated in monthly or bimonthly teleconferences and considered evidence-based updates to the 2008 ACIP recommendations. The Work Group comprised experts in diverse disciplines including laboratory, public health, and clinical specialties. Data collected, analyzed, and prepared by the Work Group were deliberated by ACIP during six public meetings. With publication of this report, the recommendations become final and are the official CDC recommendations for rabies PrEP.
Recommendations for PrEP depend on the level of a person’s risk for being exposed to rabies. The Work Group redefined risk categories into five groups, with level 1 involving activities with the highest risk and level 5 involving those with the lowest risk (Table). The highest risk categories (levels 1 and 2) include exposures that might be unrecognized (i.e., not perceived by the exposed person); for example, a small scratch to the skin during an inconspicuous personal protective equipment breach might not be noticed by persons testing neural tissue from a rabid animal or conducting ecologic studies on bats in the field. For persons with risk for unrecognized exposures, checking serial titers has historically been advised to ensure maintenance of persistently elevated rabies antibody titers; in its recent discussions, ACIP upheld this guidance because the assumption is that high titers might provide some protection when PEP is not sought for an unrecognized exposure. Recognized exposures, as defined by ACIP, are those bites, scratches, and splashes for which PEP would be sought because the exposures are usually registered by a person as unusual (e.g., contact with a bat) or painful (e.g., bite or scratch from a raccoon). The Work Group concluded that most high-risk activities involving live animals (e.g., providing veterinary health care or participating in outdoor activities in countries with endemic CRVV) are associated with only recognized exposures (risk categories 3 and 4); ACIP concluded that checking serial titers for these persons is unnecessary because recognized exposures should always prompt evaluation for PEP. Rabies vaccination recommendations for each of the redefined risk categories is summarized under Recommendations.
Risk categories might change over a person’s lifetime. Some persons for whom PrEP is indicated might have elevated risk for a limited period (e.g., during a summer internship working with wildlife or a month-long vacation to a rural village where CRVV is enzootic [risk category 4]). After the event has passed, risk level and associated recommendations for such persons will change. Shifts in risk categories are explained in the management of deviations from the recommendations section under Clinical Guidance.
A correlate of protection for rabies antibody titers has not been defined. The minimum antibody level historically recommended by ACIP is one that results in complete neutralization of rabies virus at a 1:5 serum dilution by the rapid fluorescent focus inhibition test. This is approximately equivalent to a titer of 0.1–0.3 IU/mL. Stakeholders have advocated for a specific titer value in IU/mL units of measure (rather than a range) and, ideally, one that aligns with current global guidance (i.e., that of the World Health Organization) (8). Although no infections among vaccinated persons occurred with the previous ACIP cut-off titer, most published studies use 0.5 IU/mL as a correlate of protection. This level is now endorsed by ACIP and replaces the previous minimum acceptable rabies antibody titer. The higher value provides a more conservative limit for indicating inadequate response to rabies vaccination and the need for booster doses (9).
Although there is no established correlate of protection for rabies, induction of a peak antibody response at or above the minimum acceptable antibody titer level (≥0.5 IU/mL) in response to rabies vaccine is an indirect measure of protection (i.e., immunogenicity). Primary immunogenicity refers to immunogenicity that peaks 2–4 weeks after completing the recommended vaccination or vaccinations and elicits an anamnestic response to rabies virus exposures. Since publication of the 2008 ACIP recommendations (1), scientists have been evaluating data concerning the efficacy of shorter rabies PrEP dosing regimens.
Subject matter experts performed a systematic review of scientific evidence published during 1965–2019 for a 2-dose primary vaccination series (doses administered on days 0 and 7) compared with the 3-dose series (doses administered on days 0, 7, and 21 or 28), which is indicated in the 2008 ACIP recommendations (1). Data showed that an anamnestic response after the 2-dose series occurs at 3 years (10); however, an anamnestic response >3 years after the 2-dose series has not been evaluated. In the absence of data confirming an anamnestic response, the Work Group evaluated methods of inferring long-term immunogenicity (i.e., an anamnestic response >3 years after the 2-dose primary vaccination series). Checking a titer or titers was considered one way of inferring long-term immunogenicity as described in the PrEP schedule and long-term immunogenicity section that follows. As an alternative to a titer check, a second systematic review was conducted to evaluate a booster dose after the 2-dose series compared with no booster dose. The Work Group used an adapted Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach to determine the certainty of evidence for immunogenicity rated on a scale of 1 (high certainty) to 4 (very low certainty). Within the evidence to recommendations (EtR) framework, ACIP considered the importance of rabies as a public health problem; the benefits and harms (including GRADE-assessed evidence); the target populations’ values and preferences; and issues of resource use, acceptability to stakeholders, feasibility of implementation, and anticipated impact on health equity.
PrEP schedule and primary immunogenicity. The systematic review identified 12 studies that enrolled a combined total of 1,401 subjects. Studies evaluating both IM and intradermal vaccination were included because primary immunogenicity is similar for both routes of administration (11). Using the GRADE approach, the Work Group concluded with moderate (level 2) certainty that the primary immunogenicity of the 2-dose (days 0 and 7) IM schedule is comparable to that of the 3-dose (days 0, 7, and 21 or 28) IM schedule (risk ratio = 1.00 [95% CI = 0.99–1.01]).¶ ACIP deliberated whether the 2-dose (days 0 and 7) IM PrEP schedule should replace the 3-dose schedule for all persons for whom rabies PrEP is indicated based on this finding and other findings within the EtR framework**: the target population’s acceptability of the 2-dose series, feasibility of implementing the 2-dose series, minimal resource use, and anticipated increase in health equity because the 2-dose series is less expensive than the 3-dose series.
PrEP schedule and long-term immunogenicity. Serial antibody titer checks are recommended for persons at elevated risk for unrecognized exposures. During recent discussions, ACIP upheld this recommendation advising that rabies antibody titers be checked every 6 months for persons in risk category 1 and every 2 years for persons in risk category 2. As previously noted, the main reason to maintain high titers is to provide some protection from unrecognized exposures; however, high titers also ensure an anamnestic response after an exposure (i.e., long-term immunogenicity).
For persons at sustained risk for only recognized exposures (risk category 3), checking serial antibody titers (as recommended for risk groups 1 and 2) was determined unnecessary; a one-time check of rabies antibody titer during years 1–3 after the 2-dose primary series was deemed appropriate assurance of long-term immunogenicity for persons with this risk. The rationale for this conclusion is that data indicate that an antibody titer ≥0.5 IU/mL 1 year after a rabies PrEP schedule is a marker for long-term immunogenicity (12,13), and the 2-dose series is known to be protective for at least 3 years (10).
As an alternative to the one-time titer check for risk category 3, the systematic review identified observational data from two studies that showed a booster dose triggered an anamnestic response up to 3 years after the 2-dose series. Because the third dose of the PrEP series recommended in the 2008 ACIP recommendations is given as early as day 21 and is known to provide long-term immunogenicity, a booster dose administered from day 21 to year 3 after the primary series was considered. Using the GRADE methodology, the Work Group concluded with low (level 3) certainty that a one-time booster dose of rabies vaccine during day 21–year 3 after the primary vaccination series provides better long-term immunogenicity than no booster dose; low certainty was determined because the data were not from randomized controlled trials comparing the booster with no booster.†† After evaluating these data, ACIP considered an IM booster dose of rabies vaccine during day 21–year 3 after completing the 2-dose series as an alternative to a titer check, for persons with sustained and elevated risk for recognized rabies exposures (i.e., those in risk category 3) from day 21 to year 3 after completing the 2-dose series. The rationale for the recommendation§§ within the EtR framework included the public health importance of rabies, moderately substantial desirable anticipated effect from administering a booster dose, minimal anticipated undesirable effects, acceptability to stakeholders, and feasibility of implementing the booster dose.
After considering the evidence, ACIP recommended all persons for whom rabies PrEP is indicated receive 2 IM doses of HDCV or PCECV on days 0 and 7. In addition, persons in the newly defined risk category 1 should have rabies antibody titers checked every 6 months, and those in the newly defined risk category 2 should have rabies antibody titers checked every 2 years; a booster dose should be administered if titers are <0.5 IU/mL at the time of these titer checks (Table). ACIP recommended persons in risk category 3 either have rabies antibody titers checked during years 1–3 after completion of the 2-dose primary series (and a booster dose if the titer is <0.5 IU/mL) or preemptively receive a one-time IM booster dose of rabies vaccine during day 21–year 3 after completion of the 2-dose primary series (Figure). These recommendations apply both to immunocompetent and immunocompromised persons; however, PrEP administered to immunocompromised persons requires additional considerations as described in the approach to PrEP section under the following Clinical Guidance.
The Work Group identified additional considerations that are essential to effective administration of rabies PrEP. These include coadministration of PrEP and chloroquine (or drugs related to chloroquine), the approach to PrEP in special populations, and management of deviations from the ACIP recommendations.
Coadministration of IM rabies PrEP and chloroquine or drugs related to chloroquine. Recent data show that although concomitant administration of chloroquine and IM rabies PrEP is associated with a significant reduction in rabies antibody titer, the reduced levels remain >0.5 IU/mL (14). This finding is of uncertain clinical significance because immunocompetent persons who receive chloroquine and rabies vaccines would presumably mount rabies antibody titer levels ≥0.5 IU/mL and therefore not require management that differs from that for persons who did not receive concomitant rabies vaccine. However, out of an abundance of caution and because rabies is nearly always fatal, clinicians might consider avoiding chloroquine when rabies vaccine is being administered. If avoidance is not possible, ensuring that a patient’s rabies antibody titer is ≥0.5 IU/mL no sooner than 1 week (preferably 2–4 weeks) after completion of the series will confirm that vaccination was effective. No impact on efficacy was observed in the same study when other antimalarials (i.e., Malarone [atovaquone plus proguanil] and doxycycline) were administered with IM rabies PrEP. Limited anecdotal reports suggest mefloquine does not impair rabies vaccine effectiveness (15); however, large-scale trials are needed to evaluate this hypothesis.
Approach to PrEP in special populations, including persons suspected or confirmed to be immunocompromised. Modern rabies vaccines are inactivated and have been safely administered to persons of all ages, including pregnant women and immunocompromised persons. An adequate immune response is anticipated among all immunocompetent persons (including elderly immunocompetent persons) who receive rabies vaccines in accordance with the ACIP recommendations. For this reason, proof of primary immunogenicity through laboratory confirmation is not advised for immunocompetent persons after the following actions: completion of the 2-dose primary series; administration of booster doses for serial titers <0.5 IU/mL (risk categories 1 and 2) or the one-time titer <0.5 IU/mL (risk category 3); and administration of a one-time booster dose (risk category 3).
However, among persons with primary or secondary immunodeficiencies, the immune response to vaccines, including rabies vaccines, can be suboptimal. ACIP recommends that, when possible, vaccination be delayed until a temporary immunocompromising condition has resolved or immunosuppressive medications can be withheld.¶¶ If an immunocompromising condition cannot be temporarily reversed, rabies vaccines can be administered, but antibody titer should be checked no sooner than 1 week (preferably 2–4 weeks) (10) after completion of the 2-dose PrEP series and all booster doses (including those administered within 3 years of the primary series and in response to a low titer during the serial titer checks recommended for risk categories 1 and 2). If the titer is <0.5 IU/mL, a booster dose should be administered, followed by a subsequent titer check. If two such booster doses fail to elicit an acceptable antibody titer, local or state public health authorities should be consulted for case-specific guidance. Participation in high-risk activities by persons confirmed or suspected to be immunocompromised should be avoided until the laboratory-confirmed minimum acceptable antibody titer is achieved or until public health authorities provide alternative guidance. Of note, if deviations in the ACIP recommendations occur as described in management of deviation section below, a titer check is recommended regardless of immune status.
Management of deviations from the recommendations. Unavoidable delays of a few days from the recommended date of the second dose of the 2-dose primary series are clinically inconsequential. The effect of longer lapses of 2 weeks or more is unknown. When substantial delays occur, local and state public health authorities should be consulted for guidance. The second dose of the primary series should not be administered before the recommended interval between doses has elapsed; if it is inadvertently administered earlier, local and state public health authorities should be consulted for guidance.
Persons who have not previously received rabies PrEP should identify the risk category based on their activities. If their activities change over time, the recommendations of the new risk category should be followed to ensure long-term immunogenicity. Persons in risk category 3 who do not obtain the titer check or booster dose recommended by ACIP within the specified interval can be realigned with the ACIP recommendations (i.e., they should first have a random titer checked regardless of their immune status); for some, titers remain ≥0.5 IU/mL (16) and a booster dose is not required. However, for those whose titer is <0.5 IU/mL, a booster should be administered and then titers checked no sooner than 1 week (preferably 2–4 weeks) later. Once a titer of 0.5 IU/mL is achieved, these persons should be managed the same as persons who, consistent with the ACIP recommendations, had the recommended titer or booster within 3 years of the 2-dose primary vaccination series vaccine (Figure).
Persons who have not realigned with the ACIP recommendations and have a rabies exposure require the same PEP that is recommended for persons who did not receive PrEP (i.e., rabies immunoglobulin and 4 IM doses of rabies vaccine on days 0, 3, 7, and 14) (17). After this, they are considered to have been previously vaccinated, and in response to any subsequent exposure, only require 2 doses of rabies vaccine on days 0 and 3. Similarly, persons whose risk was categorized as category 4 (e.g., because of short-term animal care work), might later in life shift to risk category 3 (e.g., because they are pursuing a veterinary career). Shifts from risk category start highlight4end highligh4 to risk category start highlight3end highlight should be managed through realignment with the ACIP recommendations described; if realignment is not done, an exposure to rabies virus should be managed with rabies immunoglobulin and the 4-dose rabies vaccine series (doses administered on days 0, 3, 7, and 14)
More persons who are recommended to receive rabies PrEP might be vaccinated because the 2-dose series recommended in these updates is associated with lower out-of-pocket costs and takes less time to complete. Persons with only short-term (≤3 years) risk for rabies (risk category 4) require no additional titer or booster doses, and last-minute travelers who previously were not vaccinated because the 3-dose series required ≥21 days might now be vaccinated because only 1 week is needed to complete the 2-dose primary series.
The updates might also facilitate improved adherence to evidence-based ACIP recommendations. As previously mentioned, in the past, some persons recommended to have serial titers checked did not adhere to those recommendations; with this update, many such persons now have the option of a one-time titer check or a one-time booster dose (i.e., a one-time action with two options for accomplishing it). As described in the EtR framework, some persons might prefer the titer option because of the potentially lower cost if a booster is not indicated (i.e., titer is ≥0.5 IU/mL); others might prefer the convenience of proceeding directly to a booster dose. The wide interval during which the titer or booster options can be taken might defray up-front costs and allow persons more time to determine whether they expect risk for rabies >3 years. Appointments for the titer check or booster dose can be scheduled at the time of the 2-dose primary series to ensure adherence to the recommendations.
Persons who received the 3-dose PrEP schedule recommended by ACIP in the past and whose activities place them within risk category 3 require no further titer checks or booster doses; the last vaccine dose they receive as part of the 3-dose series is equivalent to the option provided in these updates for a booster dose during day 21 to year 3. However, frequency of serial titer checks (risk categories 1 and 2) is unchanged, regardless of whether the 2-dose or 3-dose primary series was received by a person.
A consequence of the updated minimum acceptable rabies antibody titer (0.5 IU/mL) is that when titers are checked, more persons might require a booster dose than with the previous minimum acceptable rabies antibody titer level. ACIP concluded that the benefits of the new acceptable titer outweighed this theoretical concern.
Ongoing studies are needed to confirm long-term immunogenicity of the 2-dose PrEP series >3 years after the primary series. Studies are also needed to evaluate the frequency of and need for titer checks for persons in risk categories 1 and 2 and to examine efficacy of PrEP among immunocompromised persons.
Catherine M. Brown, Bureau of Infectious Disease and Laboratory Sciences, Massachusetts Department of Public Health; Sally Slavinski, New York City Department of Health and Mental Hygiene; Matt Zahn, Orange County Public Health; David R. Shlim, Jackson Hole Travel and Tropical Medicine; Elizabeth Barnett, Boston Medical Center; James J. Stevermer, Department of Family and Community Medicine, University of Missouri; Michael A. Pentella, State Hygienic Laboratory, University of Iowa; Paula E. Agger, Robin Levis, Center for Biologics Evaluation and Research, Food and Drug Administration; Pedro L. Moro, Division of Healthcare Quality Promotion, National Center for Emerging and Zoonotic Infectious Diseases, CDC; Kristina M. Angelo, Division of Global Migration and Quarantine, National Center for Emerging and Zoonotic Infectious Diseases, CDC; Jamie Loehr, Cayuga Family Medicine; Eun-Chung Park, National Institutes of Health; Julie Emili, Robert Stirling, Linlu Zhao, National Advisory Committee on Immunization, Public Health Agency of Canada; Karl M. Hess, Chapman University School of Pharmacy; Gregory J. Moran, Olive View-University of California, Los Angeles Medical Center.
Jesse Bonwitt, James Ellison, Michelle Kautz, Jessica MacNeil, Anna Mandra, Faisal S. Minhaj, Brett W. Petersen, Panayampalli S. Satheshkumar, Caroline Schrodt, Erin Whitehouse.
Corresponding author: Agam K. Rao, email@example.com, 404-639-3330.
1National Center for Emerging and Zoonotic Infectious Diseases, CDC; 2Kansas State University College of Veterinary Medicine, Manhattan, Kansas; 3Epidemic Intelligence Service, CDC; 4University of Arizona College of Medicine, Phoenix, Arizona; 5Department of Health Research Methods, Evidence and Impact, McMaster University, Hamilton, Ontario; 6Arkansas Department of Health; 7Minnesota Department of Health; 8Saint Louis University School of Medicine, St. Louis, Missouri.
All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. Susan M. Moore reports directorship (until September 2020) of the not-for-profit Kansas State University rabies laboratory, which performs rabies serology testing; presidency of Compass Rabies Consulting, LLC, during September 2020–January 2022, and in that role, receipt of consulting fees for advice on rabies serology testing, interpretation, and quality assurance; and since January 2022, affiliation with the University of Missouri to build a not-for-profit One Health Laboratory that will include rabies serology testing. No other potential conflicts of interest were disclosed.
- Manning SE, Rupprecht CE, Fishbein D, et al.; Advisory Committee on Immunization Practices Centers for Disease Control and Prevention. Human rabies prevention—United States, 2008: recommendations of the Advisory Committee on Immunization Practices. MMWR Recomm Rep 2008;57(No. RR-3):1–28. PMID:18496505external icon
- Hampson K, Coudeville L, Lembo T, et al. Estimating the global burden of endemic canine rabies. PLoS Negl Trop Dis 2015;9:e0003709. https://doi.org/10.1371/journal.pntd.0003709external icon
- Pieracci EG, Pearson CM, Wallace RM, et al. Vital signs: trends in human rabies deaths and exposures—United States, 1938–2018. MMWR Morb Mortal Wkly Rep 2019;68:524–8. https://doi.org/10.15585/mmwr.mm6823e1external icon PMID:31194721external icon
- Ma X, Monroe BP, Wallace RM, et al. Rabies surveillance in the United States during 2019. J Am Vet Med Assoc 2021;258:1205–20. https://doi.org/10.2460/javma.258.11.1205external icon PMID:33978439external icon
- CDC. Collected recommendations of the Public Health Service Advisory Committee on Immunization Practices. MMWR Morb Mortal Wkly Rep 1969;18:17–20.
- Blanton JD, Colwell E, Walden CL, et al. Rabies exposures and pre-exposure vaccination practices among individuals with an increased risk of rabies exposure in the United States. J Am Vet Med Assoc 2018;252:1491–502. https://doi.org/10.2460/javma.252.12.1491external icon PMID:29889644external icon
- Yates JA, Rao SR, Walker AT, et al.; Global TravEpiNet Consortium. Characteristics and preparation of the last-minute traveler: analysis of vaccine usage in the Global TravEpiNet Consortium. J Travel Med 2019;26:taz031. https://doi.org/10.1093/jtm/taz031external icon PMID:31044254external icon
- World Health Organization. WHO expert consultation on rabies: TRS no. 982. Geneva Switzerland: World Health Organization; 2013. https://www.who.int/publications/i/item/WHO-TRS-982external icon
- Moore SM. Challenges of rabies serology: defining context of interpretation. Viruses 2021;13:1516. https://doi.org/10.3390/v13081516external icon PMID:34452381external icon
- Soentjens P, Andries P, Aerssens A, et al. Preexposure intradermal rabies vaccination: a noninferiority trial in healthy adults on shortening the vaccination schedule from 28 to 7 days. Clin Infect Dis 2019;68:607–14. https://doi.org/10.1093/cid/ciy513external icon PMID:29939243external icon
- Recuenco S, Warnock E, Osinubi MOV, Rupprecht CE. A single center, open label study of intradermal administration of an inactivated purified chick embryo cell culture rabies virus vaccine in adults. Vaccine 2017;35:4315–20. https://doi.org/10.1016/j.vaccine.2017.06.083external icon PMID:28688782external icon
- Strady A, Lang J, Lienard M, Blondeau C, Jaussaud R, Plotkin SA. Antibody persistence following preexposure regimens of cell-culture rabies vaccines: 10-year follow-up and proposal for a new booster policy. J Infect Dis 1998;177:1290–5. https://doi.org/10.1086/515267external icon PMID:9593014external icon
- Mansfield KL, Andrews N, Goharriz H, et al. Rabies pre-exposure prophylaxis elicits long-lasting immunity in humans. Vaccine 2016;34:5959–67. https://doi.org/10.1016/j.vaccine.2016.09.058external icon PMID:27997343external icon
- Endy TP, Keiser PB, Cibula D, et al. Effect of antimalarial drugs on the immune response to intramuscular rabies vaccination using a postexposure prophylaxis regimen. J Infect Dis 2020;221:927–33. https://doi.org/10.1093/infdis/jiz558external icon PMID:31743394external icon
- Lau SC. Intradermal rabies vaccination and concurrent use of mefloquine. J Travel Med 1999;6:140–1. https://doi.org/10.1111/j.1708-8305.1999.tb00846.xexternal icon PMID:10381968external icon
- De Pijper CA, Langedijk AC, Terryn S, et al. Long-term memory response after a single intramuscular rabies booster vaccination, 10–24 years after primary immunization. J Infect Dis 2021. Epub January 27, 2021. https://doi.org/10.1093/infdis/jiab034external icon PMID:33502530external icon
- Rupprecht CE, Briggs D, Brown CM, et al. Evidence for a 4-dose vaccine schedule for human rabies post-exposure prophylaxis in previously non-vaccinated individuals. Vaccine 2009;27:7141–8. https://doi.org/10.1016/j.vaccine.2009.09.029external icon PMID:19925944external icon
FIGURE. Management of long-term immunogenicity* for hypothetical patients (A–E)†,§,¶ who received the Advisory Committee on Immunization Practices recommended 2-dose rabies preexposure prophylaxis schedule** and have sustained risk for recognized exposures (risk category 3) — Advisory Committee on Immunization Practices, United States, 2022
Abbreviations: ACIP = Advisory Committee on Immunization Practices; IM = intramuscular injection; IU = international units; PEP = postexposure prophylaxis; PrEP = preexposure prophylaxis; RIG = rabies immunoglobulin.
* Long-term immunogenicity is considered a successful anamnestic response (i.e., rapid rise in antibody levels) after an encounter with the rabies virus antigen >3 years after the primary vaccination series.
† Patient A received the recommended booster dose during day 21–year 3 and patients B and C received the recommended one-time titer check during years 1–3. Recommended options for patients A–C include 1) a one-time rabies vaccine booster dose from day 21 to 3 years after the 2-dose primary series (patient A) and 2) a one-time rabies antibody titer check 1–3 years after the 2-dose primary series (patients B and C).
§ Patient D did not receive the recommended one-time titer or booster dose but was realigned to the ACIP recommendations before an exposure occurred. Realigning involves checking a titer. If the titer is ≥0.5 IU/mL, no further action is needed, and the patient is considered realigned with the ACIP recommendations. If the titer is <0.5 IU/mL, patient D should receive a booster dose followed by an additional titer no sooner than 1 week later (preferably 2-4 weeks later) to confirm the appropriate response.
¶ Patient E did not receive the recommended one-time titer or booster dose and had an exposure before they could be realigned to the ACIP recommendations. This patient should receive RIG and the 4-dose rabies vaccine PEP series indicated for persons not previously vaccinated.
** An acceptable antibody titer (i.e., ≥0.5 IU/mL) should be confirmed after boosters are administered to immunocompromised persons.
Suggested citation for this article: Rao AK, Briggs D, Moore SM, et al. Use of a Modified Preexposure Prophylaxis Vaccination Schedule to Prevent Human Rabies: Recommendations of the Advisory Committee on Immunization Practices — United States, 2022. MMWR Morb Mortal Wkly Rep 2022;71:619–627. DOI: http://dx.doi.org/10.15585/mmwr.mm7118a2external icon.
MMWR and Morbidity and Mortality Weekly Report are service marks of the U.S. Department of Health and Human Services.
Use of trade names and commercial sources is for identification only and does not imply endorsement by the U.S. Department of Health and Human Services.
References to non-CDC sites on the Internet are provided as a service to MMWR readers and do not constitute or imply endorsement of these organizations or their programs by CDC or the U.S. Department of Health and Human Services. CDC is not responsible for the content of pages found at these sites. URL addresses listed in MMWR were current as of the date of publication.
All HTML versions of MMWR articles are generated from final proofs through an automated process. This conversion might result in character translation or format errors in the HTML version. Users are referred to the electronic PDF version (https://www.cdc.gov/mmwr) and/or the original MMWR paper copy for printable versions of official text, figures, and tables.
Questions or messages regarding errors in formatting should be addressed to firstname.lastname@example.org.