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|a dc
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|a Tostanoski, Lisa H.
|e author
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|a Massachusetts Institute of Technology. Department of Biological Engineering
|e contributor
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|a Wegmann, Frank
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|a Martinot, Amanda J.
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|a Loos, Carolin
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|a McMahan, Katherine
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|a Mercado, Noe B.
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|a Yu, Jingyou
|e author
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|a Chan, Chi N.
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|a Bondoc, Stephen
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|a Starke, Carly E.
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|a Nekorchuk, Michael
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|a Busman-Sahay, Kathleen
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|a Piedra-Mora, Cesar
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|a Wrijil, Linda M.
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|a Ducat, Sarah
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|a Custers, Jerome
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|a Atyeo, Caroline
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|a Fischinger, Stephanie
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|a Burke, John S.
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|a Feldman, Jared
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|a Hauser, Blake M.
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|a Caradonna, Timothy M.
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|a Bondzie, Esther A.
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|a Dagotto, Gabriel
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|a Gebre, Makda S.
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|a Jacob-Dolan, Catherine
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|a Lin, Zijin
|e author
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|a Mahrokhian, Shant H.
|e author
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|a Nampanya, Felix
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|a Nityanandam, Ramya
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|a Pessaint, Laurent
|e author
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|a Porto, Maciel
|e author
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|a Ali, Vaneesha
|e author
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|a Benetiene, Dalia
|e author
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|a Tevi, Komlan
|e author
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|a Andersen, Hanne
|e author
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|a Lewis, Mark G.
|e author
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|a Schmidt, Aaron G.
|e author
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|a Lauffenburger, Douglas A
|e author
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|a Alter, Galit
|e author
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|a Estes, Jacob D.
|e author
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|a Schuitemaker, Hanneke
|e author
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|a Zahn, Roland
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|a Barouch, Dan H.
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|a Ad26 vaccine protects against SARS-CoV-2 severe clinical disease in hamsters
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|c 2020-09-08T21:07:15Z.
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|z Get fulltext
|u https://hdl.handle.net/1721.1/127202
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|a Coronavirus disease 2019 (COVID-19) in humans is often a clinically mild illness, but some individuals develop severe pneumonia, respiratory failure and death. Studies of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in hamsters and nonhuman primates have generally reported mild clinical disease, and preclinical SARS-CoV-2 vaccine studies have demonstrated reduction of viral replication in the upper and lower respiratory tracts in nonhuman primates. Here we show that high-dose intranasal SARS-CoV-2 infection in hamsters results in severe clinical disease, including high levels of virus replication in tissues, extensive pneumonia, weight loss and mortality in a subset of animals. A single immunization with an adenovirus serotype 26 vector-based vaccine expressing a stabilized SARS-CoV-2 spike protein elicited binding and neutralizing antibody responses and protected against SARS-CoV-2-induced weight loss, pneumonia and mortality. These data demonstrate vaccine protection against SARS-CoV-2 clinical disease. This model should prove useful for preclinical studies of SARS-CoV-2 vaccines, therapeutics and pathogenesis.
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|a Article
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|t Nature Medicine
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