Reference Database

YearReference
2021
Low-dose Ad26.COV2.S protection against SARS-CoV-2 challenge in rhesus macaques.
He, Xuan
Chandrashekar, Abishek
Zahn, Roland
Wegmann, Frank
Yu, Jingyou
Mercado, Noe B
McMahan, Katherine
Martinot, Amanda J
Piedra-Mora, Cesar
Beecy, Sidney
Ducat, Sarah
Chamanza, Ronnie
Huber, Sietske Rosendahl
van Heerden, Marjolein
van der Fits, Leslie
Borducchi, Erica N
Lifton, Michelle
Liu, Jinyan
Nampanya, Felix
Patel, Shivani
Peter, Lauren
Tostanoski, Lisa H
Pessaint, Laurent
Van Ry, Alex
Finneyfrock, Brad
Velasco, Jason
Teow, Elyse
Brown, Renita
Cook, Anthony
Andersen, Hanne
Lewis, Mark G
Schuitemaker, Hanneke
Barouch, Dan H
Cell 2021 06 24;184: 3467-3473.e11
Abstract

We previously reported that a single immunization with an adenovirus serotype 26 (Ad26)-vector-based vaccine expressing an optimized SARS-CoV-2 spike (Ad26.COV2.S) protected rhesus macaques against SARS-CoV-2 challenge. To evaluate reduced doses of Ad26.COV2.S, 30 rhesus macaques were immunized once with 1 × 10, 5 × 10, 1.125 × 10, or 2 × 10 viral particles (vp) Ad26.COV2.S or sham and were challenged with SARS-CoV-2. Vaccine doses as low as 2 × 10 vp provided robust protection in bronchoalveolar lavage, whereas doses of 1.125 × 10 vp were required for protection in nasal swabs. Activated memory B cells and binding or neutralizing antibody titers following vaccination correlated with protective efficacy. At suboptimal vaccine doses, viral breakthrough was observed but did not show enhancement of disease. These data demonstrate that a single immunization with relatively low dose of Ad26.COV2.S effectively protected against SARS-CoV-2 challenge in rhesus macaques, although a higher vaccine dose may be required for protection in the upper respiratory tract.

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