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Evaluation of the immunogenicity and efficacy of an rVSV vaccine against Zika virus infection in macaca nemestrina.
- Source :
- Frontiers in Virology; 2/28/2023, p1-11, 11p
- Publication Year :
- 2023
-
Abstract
- Zika virus (ZIKV) is a mosquito-borne flavivirus that causes an acute febrile illness. ZIKV can be transmitted between sexual partners and from mother to fetus. Infection is strongly associated with neurologic complications in adults, including Guillain-Barre' syndrome and myelitis, and congenital ZIKV infection can result in fetal injury and congenital Zika syndrome (CZS). Development of an effective vaccine is imperative to protect against ZIKV vertical transmission and CZS. Recombinant Vesicular Stomatitis virus (rVSV) is a highly effective and safe vector for the delivery of foreign immunogens for vaccine purposes. Here, we evaluate an rVSV vaccine expressing the full length pre-membrane (prM) and ZIKV envelope (E) proteins (rVSVDM-ZprME), shown to be immunogenic in murine models of ZIKV infection, for its capacity to induce immune responses in nonhuman primates. Moreover, we assess the efficacy of the rVSVDM-ZprME vaccine in the protection of pigtail macaques against ZIKV infection. Administration of the rVSVDM-ZprME vaccine was safe, but it did not induce robust anti-ZIKV T-cell responses, IgM or IgG antibodies, or neutralizing antibodies in most animals. Post ZIKV challenge, animals that received the rVSVDM control vaccine lacking ZIKV antigen had higher levels of plasma viremia compared to animals that received the rVSVDM-ZprME vaccine. Anti-ZIKV neutralizing Ab titers were detected in a single animal that received the rVSVDM-ZprME vaccine that was associated with reduced plasma viremia. The overall suboptimal ZIKV-specific cellular and humoral responses postimmunization indicates the rVSVDM-ZprME vaccine did not elicit an immune response in this pilot study. However, recall antibody response to the rVSVDMZprME vaccine indicates it may be immunogenic and further developments to the vaccine construct could enhance its potential as a vaccine candidate in a nonhuman primate pre-clinical model. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 2673818X
- Database :
- Complementary Index
- Journal :
- Frontiers in Virology
- Publication Type :
- Academic Journal
- Accession number :
- 174397804
- Full Text :
- https://doi.org/10.3389/fviro.2023.1108420