作者
Abishek Chandrashekar, Jinyan Liu, Amanda J Martinot, Katherine McMahan, Noe B Mercado, Lauren Peter, Lisa H Tostanoski, Jingyou Yu, Zoltan Maliga, Michael Nekorchuk, Kathleen Busman-Sahay, Margaret Terry, Linda M Wrijil, Sarah Ducat, David R Martinez, Caroline Atyeo, Stephanie Fischinger, John S Burke, Matthew D Slein, Laurent Pessaint, Alex Van Ry, Jack Greenhouse, Tammy Taylor, Kelvin Blade, Anthony Cook, Brad Finneyfrock, Renita Brown, Elyse Teow, Jason Velasco, Roland Zahn, Frank Wegmann, Peter Abbink, Esther A Bondzie, Gabriel Dagotto, Makda S Gebre, Xuan He, Catherine Jacob-Dolan, Nicole Kordana, Zhenfeng Li, Michelle A Lifton, Shant H Mahrokhian, Lori F Maxfield, Ramya Nityanandam, Joseph P Nkolola, Aaron G Schmidt, Andrew D Miller, Ralph S Baric, Galit Alter, Peter K Sorger, Jacob D Estes, Hanne Andersen, Mark G Lewis, Dan H Barouch
发表日期
2020/8/14
期刊
Science
卷号
369
期号
6505
页码范围
812-817
出版商
American Association for the Advancement of Science
简介
An understanding of protective immunity to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is critical for vaccine and public health strategies aimed at ending the global coronavirus disease 2019 (COVID-19) pandemic. A key unanswered question is whether infection with SARS-CoV-2 results in protective immunity against reexposure. We developed a rhesus macaque model of SARS-CoV-2 infection and observed that macaques had high viral loads in the upper and lower respiratory tract, humoral and cellular immune responses, and pathologic evidence of viral pneumonia. After the initial viral clearance, animals were rechallenged with SARS-CoV-2 and showed 5 log10 reductions in median viral loads in bronchoalveolar lavage and nasal mucosa compared with after the primary infection. Anamnestic immune responses after rechallenge suggested that protection was mediated by immunologic …
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