Antibody evolution to SARS-CoV-2 after single-dose Ad26.COV2.S vaccine in humans

人类接种单剂Ad26.COV2.S疫苗后针对SARS-CoV-2的抗体演变

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作者:Alice Cho # ,Frauke Muecksch # ,Zijun Wang # ,Tarek Ben Tanfous ,Justin DaSilva ,Raphael Raspe ,Brianna Johnson ,Eva Bednarski ,Victor Ramos ,Dennis Schaefer-Babajew ,Irina Shimeliovich ,Juan P Dizon ,Kai-Hui Yao ,Fabian Schmidt ,Katrina G Millard ,Martina Turroja ,Mila Jankovic ,Thiago Y Oliveira ,Anna Gazumyan ,Christian Gaebler ,Marina Caskey ,Theodora Hatziioannou ,Paul D Bieniasz ,Michel C Nussenzweig

Abstract

The single-dose Ad.26.COV.2 (Janssen) vaccine elicits lower levels of neutralizing antibodies and shows more limited efficacy in protection against infection than either of the two available mRNA vaccines. In addition, Ad.26.COV.2 has been less effective in protection against severe disease during the Omicron surge. Here, we examined the memory B cell response to single-dose Ad.26.COV.2 vaccination. Compared with mRNA vaccines, Ad.26.COV.2 recipients had significantly lower numbers of RBD-specific memory B cells 1.5 or 6 mo after vaccination. Despite the lower numbers, the overall quality of the memory B cell responses appears to be similar, such that memory antibodies elicited by both vaccine types show comparable neutralizing potency against SARS-CoV-2 Wuhan-Hu-1, Delta, and Omicron BA.1 variants. The data help explain why boosting Ad.26.COV.2 vaccine recipients with mRNA vaccines is effective and why the Ad26.COV2.S vaccine can maintain some protective efficacy against severe disease during the Omicron surge.

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