Novel Treatment of a Vaccinia Virus Infection from an Occupational Needlestick — San Diego, California, 2019
Weekly / October 25, 2019 / 68(42);943–946
Erin R. Whitehouse, PhD1,2; Agam K. Rao, MD1; Yon C. Yu, PharmD3; Patricia A. Yu, MPH3; Margaret Griffin, MPH4; Susan Gorman, PharmD4; Kristen A. Angel, MPH5; Eric C. McDonald, MD5; Anna Liza Manlutac6; Marie A. de Perio, MD7; Andrea M. McCollum, PhD1; Whitni Davidson, MPH1; Kimberly Wilkins1; Eddy Ortega1; Panayampalli S. Satheshkumar, PhD1; Michael B. Townsend, PhD1; Marcia Isakari, MD8; Brett W. Petersen, MD1 (View author affiliations)View suggested citation
What is already known about this topic?
Inadvertent exposure to the virus Vaccinia, an orthopoxvirus used in biomedical research, can cause considerable injury and time lost from work. Vaccination is recommended for laboratorians using replication-competent vaccinia virus; however, laboratories set their own policies.
What is added by this report?
Tecovirimat, a novel antiviral approved for treatment of smallpox, and vaccinia immunoglobulin were used to safely treat an occupational exposure in an unvaccinated laboratorian who was excluded from work for 4 months.
What are the implications for public health practice?
Laboratories should ensure that workers are informed of the risks associated with manipulation of vaccinia virus and should counsel workers about the potential benefits of vaccination received according to current guidelines.
Views equals page views plus PDF downloads
- PDF pdf icon[126K] [PDF]
Vaccinia virus (VACV) is an orthopoxvirus used in smallpox vaccines, as a vector for novel cancer treatments, and for experimental vaccine research (1). The Advisory Committee on Immunization Practices (ACIP) recommends smallpox vaccination for laboratory workers who handle replication-competent VACV (1). For bioterrorism preparedness, the U.S. government stockpiles tecovirimat, the first Food and Drug Administration–approved antiviral for treatment of smallpox (caused by variola virus and globally eradicated in 1980*,†) (2). Tecovirimat has activity against other orthopoxviruses and can be administered under a CDC investigational new drug protocol. CDC was notified about an unvaccinated laboratory worker with a needlestick exposure to VACV, who developed a lesion on her left index finger. CDC and partners performed laboratory confirmation, contacted the study sponsor to identify the VACV strain, and provided oversight for the first case of laboratory-acquired VACV treated with tecovirimat plus intravenous vaccinia immunoglobulin (VIGIV). This investigation highlights 1) the misconception among laboratory workers about the virulence of VACV strains; 2) the importance of providing laboratorians with pathogen information and postexposure procedures; and 3) that although tecovirimat can be used to treat VACV infections, its therapeutic benefit remains unclear.
In December 2018, a healthy female laboratorian aged 26 years, after injecting VACV into the tail of a mouse, sustained a needlestick injury to her left index finger from the same needle. The worker immediately rinsed her finger with water for 15 minutes, notified her supervisors, and visited a local emergency department at the recommendation of a supervisor. In September 2018, before starting working with VACV, she received one-on-one counseling with an occupational health physician about the risks associated with working with VACV and was offered vaccination with ACAM2000 (Emergent BioSolutions), but she declined.
Between days 2 and 9 post infection, the patient was evaluated by two community physicians; neither advised her to observe contact precautions to prevent auto-inoculation or secondary transmission. On day 10, she was evaluated at an occupational health clinic with swelling and a single vesicular lesion at the needlestick site. The treating physician contacted CDC and the County of San Diego Health and Human Services Agency, which advised monitoring her for evidence of worsening infection. On day 12, she was treated at a university-based emergency department for fever (100.9°F [38.3°C]), left axillary lymphadenopathy, malaise, pain, and worsening edema of her finger. Health care providers were concerned about progression to compartment syndrome (excessive pressure in an enclosed muscle space, resulting from swelling after an injury), joint infection, or further spread. The specific VACV strain had not been determined, and its effect on the severity of the infection could not be predicted. Because of concern about her worsening symptoms, on day 12, the patient received a single 6,000 IU/kg dose of VIGIV and was started on a 14-day course of twice-daily (600 mg per dose) oral tecovirimat. She also received clindamycin and cephalexin because of concern about possible secondary bacterial infection. Within 48 hours of treatment initiation, the fever and lymphadenopathy resolved, and the local pain and edema decreased. During treatment with tecovirimat and antibiotics, the patient experienced mild side effects (i.e., nausea, loss of appetite, fatigue, myalgia, and pruritus), and pain in her left finger and arm. The occupational health office excluded the patient from laboratory work for approximately 4 months because of local necrosis and the risk for VACV transmission. Areas of necrotic tissue did not fully resolve until day 94 (Figure). Although the patient was not adequately counseled about transmission risk until 10 days after her injury, no secondary transmission or auto-inoculation occurred.
Laboratory verification of VACV infection was performed to rule out other sources of infection, given that the needle pierced a mouse’s tail before piercing the patient’s skin. Swabs collected from the surface of the lesion on days 10 and 12 were submitted to the County of San Diego Public Health Laboratory. Neither sample contained sufficient material for testing. On day 13, the lesion suppurated, and a swab was obtained. Nonvariola orthopoxvirus DNA signatures were amplified using real-time polymerase chain reaction (PCR) testing (Table) (3). Additional samples collected from the lesion amplified VACV-specific DNA signatures by real-time PCR. VACV was also obtained by viral culture. Serial serum samples were collected and anti-orthopoxvirus immunoglobulin G and immunoglobulin M antibodies were both present by postexposure day 25 (4). The positive immunoglobulin G finding on day 25 and 32 likely reflected administration of VIGIV.
Occupational Health Investigation
Neither the patient nor the occupational health physician could specify the concentration or strain of VACV preparation used by the patient. Upon inquiry, the study sponsor informed investigators that one of two genetically altered Western Reserve strains could have been involved.§ The patient was injecting multiple groups of mice with different strains and did not recall which strain she used when the needlestick injury occurred.
Although the patient had declined vaccination when it was initially offered, during this investigation she reported that she did not appreciate the extent of infection that could occur with VACV when vaccination was first offered. She also cited the challenges of managing the infectious lesion at the vaccination site and potential vaccination adverse events as factors contributing to her initial decision to decline vaccination.
This case was the first use of tecovirimat for a laboratory-acquired VACV infection. Tecovirimat was well tolerated by the patient with mild side effects, even with concurrently administered antibiotics. The patient’s clinical course was similar to previously reported VACV needlestick injuries, but the recovery period was longer (earlier cases resolved within 1–2 months) (5–8). The VACV strains used by the patient are not known to have heightened virulence, but whether the clinical course would have worsened without VIGIG or tecovirimat is not known. The independent effect of tecovirimat on the clinical course cannot be determined, and whether its use for similar VACV infections would be warranted is not known.
ACIP recommends vaccination for laboratorians who work with replication-competent VACV, unless vaccination is medically contraindicated (1); however, laboratories working with VACV set their own policies. ACAM2000 is a live-virus vaccine that produces an infectious vaccination site lesion. The vaccine has very low and known risk of complications for the vaccinee and close contacts (1). Appropriate vaccination site care requires careful monitoring of the site and adherence to infection control precautions until the crust separates and a new layer of skin forms.
Counseling before working with VACV needs to include benefits of vaccination, risks of working with VACV in the laboratory, vaccination-associated adverse events, care of the vaccination site, and contraindications to vaccination. Even with counseling, laboratorians might have incomplete understanding of the risks and benefits of vaccination. If the vaccine is medically contraindicated, occupational health providers and laboratorians need to carefully weigh whether continued work with replication-competent VACV is prudent. The complexity of managing a vaccination site might dissuade laboratorians from choosing to receive vaccination. However, accidental inoculations often occur in fingers or eyes, causing infections that present special concern for complications, and clinical management can be difficult (8). In addition, laboratory exposures, unlike vaccination, do not have a controlled route of exposure or controlled dose. Previous occupationally acquired VACV infections in unvaccinated workers have required hospitalization, antibiotics for secondary infections, debridement of wounds, and monitoring for functional loss of joints, digits, and vision (5,8). In one case in which recent vaccination did not fully prevent infection, it did reduce the risk for complications, decrease lesion size, and lead to faster recovery (7).
Laboratorians might also underestimate the infection risk from genetically altered, purportedly attenuated VACV strains. Recombinant VACV strains can contain genetic inserts that have unknown or adverse effects on virulence, infectivity, and wound healing (9). Most reports of laboratory-acquired VACV infections were caused by thymidine kinase–deletion strains, which are sometimes mistakenly thought to be avirulent or unlikely to cause human infections (5,8–10).
Researchers working with orthopoxviruses need to have information about the virus strains with which they are working and be provided with procedures to follow in the event of an exposure. Information about the specific strain of the VACV can help health care providers and public health officials determine the risks for complications and develop appropriate treatment plans should an infection occur. Laboratories need to implement biosafety policies and procedures and ensure that all personnel are adequately trained and aware of the risks associated with the work they perform (10). It is important that biosafety information be posted in the laboratory and adequate disinfectant is available. Providing adequate counseling to laboratorians on vaccination and prompt postexposure assessments requires coordination among laboratories, research universities, and medical providers. In the case reported here, the patient did not initiate contact precautions to prevent auto-inoculation or secondary transmission until treated by an occupational health specialist 10 days after the exposure. Clear postexposure procedures can help ensure prompt care by providers knowledgeable about the treatment of VACV exposures, including implementation of infection control practices to prevent secondary transmission.
Corresponding author: Erin R. Whitehouse, EWhitehouse@cdc.gov, 404-718-7234.
1Division of High Consequence Pathogens and Pathology, National Center for Emerging and Zoonotic Infectious Diseases, CDC; 2Epidemic Intelligence Service, CDC; 3Division of Preparedness and Emerging Infections, National Center for Emerging and Zoonotic Infectious Diseases, CDC; 4Division of Strategic National Stockpile, Assistant Secretary for Preparedness and Response, U.S. Department of Health and Human Services; 5County of San Diego Health and Human Services Agency, San Diego, California; 6County of San Diego Public Health Laboratory, San Diego, California; 7Division of Field Studies and Engineering, National Institute for Occupational Safety and Health, CDC; 8Center of Occupational and Environmental Medicine, University of California San Diego Health, San Diego, California
All authors have completed and submitted the International Committee of Medical Journal Editors form for disclosure of potential conflicts of interest. Marcia Isakari’s institution received consulting fees for posttreatment laboratory testing of this patient by the contract research organization sponsored by the study manufacturer of vaccinia virus. No other potential conflicts of interest were disclosed.
* https://apps.who.int/iris/handle/10665/39253external icon.
† https://apps.who.int/iris/handle/10665/68285external icon.
§ One strain had a deletion of the thymidine kinase gene; the second had a deletion of the thymidine kinase gene and insertion of mouse hydroxyprostaglandin dehydrogenase 15-(NAD) gene.
- Petersen BW, Harms TJ, Reynolds MG, Harrison LH. Use of vaccinia virus smallpox vaccine in laboratory and health care personnel at risk for occupational exposure to orthopoxviruses—recommendations of the Advisory Committee on Immunization Practices (ACIP), 2015. MMWR Morb Mortal Wkly Rep 2016;65:257–62. CrossRefexternal icon PubMedexternal icon
- Grosenbach DW, Honeychurch K, Rose EA, et al. Oral tecovirimat for the treatment of smallpox. N Engl J Med 2018;379:44–53. CrossRefexternal icon PubMedexternal icon
- Li Y, Olson VA, Laue T, Laker MT, Damon IK. Detection of monkeypox virus with real-time PCR assays. J Clin Virol 2006;36:194–203. CrossRefexternal icon PubMedexternal icon
- Karem KL, Reynolds M, Braden Z, et al. Characterization of acute-phase humoral immunity to monkeypox: use of immunoglobulin M enzyme-linked immunosorbent assay for detection of monkeypox infection during the 2003 North American outbreak. Clin Diagn Lab Immunol 2005;12:867–72. PubMedexternal icon
- CDC. Laboratory-acquired vaccinia exposures and infections—United States, 2005–2007. MMWR Morb Mortal Wkly Rep 2008;57:401–4. PubMedexternal icon
- Davies E, Peake L, Woolard D, et al. Laboratory-acquired vaccinia virus infection—Virginia, 2008. MMWR Morb Mortal Wkly Rep 2009;58:797–800. PubMedexternal icon
- Hsu CH, Farland J, Winters T, et al. Laboratory-acquired vaccinia virus infection in a recently immunized person—Massachusetts, 2013. MMWR Morb Mortal Wkly Rep 2015;64:435–8. PubMedexternal icon
- MacNeil A, Reynolds MG, Damon IK. Risks associated with vaccinia virus in the laboratory. Virology 2009;385:1–4. CrossRefexternal icon PubMedexternal icon
- Mempel M, Isa G, Klugbauer N, et al. Laboratory acquired infection with recombinant vaccinia virus containing an immunomodulating construct. J Invest Dermatol 2003;120:356–8. CrossRefexternal icon PubMedexternal icon
- Su CP, de Perio MA, Cummings KJ, McCague AB, Luckhaupt SE, Sweeney MH. Case investigations of infectious diseases occurring in workplaces, United States, 2006–2015. Emerg Infect Dis 2019;25:397–405. CrossRefexternal icon PubMedexternal icon
FIGURE. Progression of vaccinia virus infection at 11, 25, 57, and 94 days after an occupational needlestick exposure in December 2018 — San Diego, California, January–April 2019
Suggested citation for this article: Whitehouse ER, Rao AK, Yu YC, et al. Novel Treatment of a Vaccinia Virus Infection from an Occupational Needlestick — San Diego, California, 2019. MMWR Morb Mortal Wkly Rep 2019;68:943–946. DOI: http://dx.doi.org/10.15585/mmwr.mm6842a2external 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 email@example.com.