scholarly journals MECHANISM OF RECOVERY FROM SYSTEMIC VACCINIA VIRUS INFECTION

1972 ◽  
Vol 136 (2) ◽  
pp. 277-290 ◽  
Author(s):  
M. Worthington ◽  
A. S. Rabson ◽  
S. Baron

Administration of Cytoxan in doses capable of inhibiting both humoral and cellular immunity markedly potentiated primary systemic vaccinia virus infection in mice. Immunosuppressed mice did not form neutralizing antibody to vaccinia virus and had a prolonged and more severe viremia than nonimmunosuppressed control mice. Passive transfer of physiologic amounts of neutralizing antibody late in the course of infection, at a time when nonimmunosuppressed mice had similar levels of serum antibody, largely reversed the effect of Cytoxan on vaccinia virus infection. Transfer of 100 million immune spleen cells was much less effective than antibody in reversing the effect of Cytoxan on vaccinia virus infection, and mice receiving these cells did make some antibody. Serum interferon levels were not affected by Cytoxan. The results suggest an essential role for humoral antibody, but not for cellular immunity, in recovery from primary vaccinia virus infection in the mouse.

2010 ◽  
Vol 16 (6) ◽  
pp. 976-979 ◽  
Author(s):  
Jônatas S. Abrahão ◽  
André T. Silva-Fernandes ◽  
Larissa S. Lima ◽  
Rafael K. Campos ◽  
Maria I.M.C. Guedes ◽  
...  

Nature ◽  
1976 ◽  
Vol 259 (5540) ◽  
pp. 228-230 ◽  
Author(s):  
FEDERICO GARRIDO ◽  
VOLKER SCHIRRMACHER ◽  
HILLIARD FESTENSTEIN

2019 ◽  
Vol 6 (Supplement_2) ◽  
pp. S434-S434
Author(s):  
Erin R Whitehouse ◽  
Agam Rao ◽  
Yon Yu ◽  
Patricia Yu ◽  
Margaret Griffin ◽  
...  

Abstract Background Vaccinia virus, a virus similar to but less virulent than variola virus, is a component of smallpox vaccines and increasingly used for medical research. Vaccinia immunoglobulin intravenous (VIGIV) and tecovirimat are stockpiled in the U.S. Strategic National Stockpile (SNS) for potential smallpox bioterror events, but only VIGIV is licensed for vaccinia treatment. On January 12, 2019, CDC was consulted for worsening infection in a laboratory worker after a needlestick with vaccinia. Methods We investigated demographic, clinical, vaccination, and exposure history and determined likelihood of vaccinia virus infection. Identity of the specific strain was sought because some have genetic modifications that might impact virulence. Discussions among stakeholders informed treatment decisions and facilitated medication access and usage. Swabs from the lesion were tested by real-time polymerase chain reaction for orthopoxvirus DNA, which includes vaccinia. Results The affected worker was an otherwise healthy 26-year-old woman who developed a pustular lesion at the needlestick site on her left index finger (Image). The patient had been injecting vaccinia virus into a mouse and had declined nationally recommended vaccination. Edema, lymphadenopathy, and fever raised concern for severe illness; neither the patient nor occupational health were certain of the vaccinia strain type. CDC, SNS, local health departments, drug manufacturers, and clinicians rapidly collaborated to make treatment decisions based on available information and ensure delivery of both biologics and administration of tecovirimat under an expanded access investigational new drug protocol. Eventually, a wound swab tested positive and the strain was determined to be one with no known impact on virulence. Conclusion With increasing use of vaccinia in research, occupational infections may continue to occur. Health clinics should extensively counsel staff who decline vaccination and have documentation on-hand about vaccinia virus types to inform treatment decisions. This response prompted CDC to develop outreach materials specifically for occupational vaccinia exposures. Disclosures All authors: No reported disclosures.


2005 ◽  
Vol 41 (1) ◽  
pp. 59 ◽  
Author(s):  
Dania M. Vázquez-Blomquist ◽  
Diógenes Quintana-Vázquez ◽  
Ernesto Galbán Rodríguez ◽  
Antonieta M. Herrera Buch ◽  
Carlos A. Duarte Cano

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