A Single-Dose Intranasal ChAd Vaccine Protects Upper and Lower Respiratory Tracts against SARS-CoV-2.
СтатьяПоддержка NIH: внешняя программаНазвание и аннотация: Перевод в очереди
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Hassan Ahmed O, Kafai Natasha M, Dmitriev Igor P, Fox Julie M, Smith Brittany K, Harvey Ian B, Chen Rita E, Winkler Emma S, Wessel Alex W, Case James Brett, Kashentseva Elena, McCune Broc T, Bailey Adam L, Zhao Haiyan, VanBlargan Laura A, Dai Ya-Nan, Ma Meisheng, Adams Lucas J, Shrihari Swathi, Danis Jonathan E, Gralinski Lisa E, Hou Yixuan J, Schäfer Alexandra, Kim Arthur S, Keeler Shamus P, Weiskopf Daniela, Baric Ralph S, Holtzman Michael J, Fremont Daved H, Curiel David T, Diamond Michael S
Аннотация
The coronavirus disease 2019 pandemic has made deployment of an effective vaccine a global health priority. We evaluated the protective activity of a chimpanzee adenovirus-vectored vaccine encoding a prefusion stabilized spike protein (ChAd-SARS-CoV-2-S) in challenge studies with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and mice expressing the human angiotensin-converting enzyme 2 receptor. Intramuscular dosing of ChAd-SARS-CoV-2-S induces robust systemic humoral and cell-mediated immune responses and protects against lung infection, inflammation, and pathology but does not confer sterilizing immunity, as evidenced by detection of viral RNA and induction of anti-nucleoprotein antibodies after SARS-CoV-2 challenge. In contrast, a single intranasal dose of ChAd-SARS-CoV-2-S induces high levels of neutralizing antibodies, promotes systemic and mucosal immunoglobulin A (IgA) and T cell responses, and almost entirely prevents SARS-CoV-2 infection in both the upper and lower respiratory tracts. Intranasal administration of ChAd-SARS-CoV-2-S is a candidate for preventing SARS-CoV-2 infection and transmission and curtailing pandemic spread.