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DOI 10.1016/j.celrep.2019.01.052

Медицинская библиотека · Cell reports · 2019

Dengue and Zika Virus Cross-Reactive Human Monoclonal Antibodies Protect against Spondweni Virus Infection and Pathogenesis in Mice.

Salazar Vanessa, Jagger Brett W, Mongkolsapaya Juthathip, Burgomaster Katherine E, Dejnirattisai Wanwisa, Winkler Emma S, Fernandez Estefania, Nelson Christopher A, Fremont Daved H, Pierson Theodore C, Crowe James E, Screaton Gavin R, Diamond Michael S

СтатьяПоддержка NIH: внешняя программаResearch Support, N.I.H., IntramuralПоддержка исследования: вне правительства СШАПеревод в очереди

Аннотация

Spondweni virus (SPOV) is the flavivirus that is most closely related to Zika virus (ZIKV). Although SPOV causes sporadic human infections in Africa, recently it was found in Culex mosquitoes in Haiti. To investigate the pathogenic spectrum of SPOV, we developed infection models in mice. Although two SPOV strains failed to cause disease in immunocompetent mice, each accumulated in the brain, spleen, eye, testis, and kidney when type I interferon signaling was blocked and unexpectedly caused infection, immune cell infiltration, and swelling in the ankle. In pregnant mice, SPOV replicated in the placenta and fetus but did not cause placental insufficiency or microcephaly. We identified human antibodies from ZIKV or DENV immune subjects that neutralized SPOV infection and protected against lethal challenge. Our experiments describe similarities and differences in clinical syndromes between SPOV and ZIKV and suggest that their serological relatedness has implications for antibody therapeutics and flavivirus vaccine development.

Для цитирования: Salazar Vanessa, Jagger Brett W, Mongkolsapaya Juthathip, Burgomaster Katherine E, Dejnirattisai Wanwisa, Winkler Emma S, Fernandez Estefania, Nelson Christopher A, Fremont Daved H, Pierson Theodore C, Crowe James E, Screaton Gavin R, Diamond Michael S. Dengue and Zika Virus Cross-Reactive Human Monoclonal Antibodies Protect against Spondweni Virus Infection and Pathogenesis in Mice.. Cell reports. 2019. DOI: 10.1016/j.celrep.2019.01.052.

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