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Prolonged evolution of the memory B cell response induced by a replicating adenovirus-influenza H5 vaccine.

Kenta MatsudaJinghe HuangTongqing ZhouZizhang ShengByong Ha KangElise IshidaTrevor GriesmanSarah StuccioLyuba BolkhovitinovTeddy J WohlboldVeronika ChromikovaAlberto CagigiKwanyee LeungSarah F AndrewsCrystal S F CheungAlyssa A PullanoJason PlylerCinque SotoBaoshan ZhangYongping YangM Gordon JoyceYaroslav TsybovskyAdam K WheatleySandeep R NarpalaYicheng GuoSam DarkoRobert T BailerApril PooleC Jason LiangJon SmithJeff AlexanderMarc GurwithStephen A MiguelesRichard A KoupHana GoldingSurender KhuranaAdrian B McDermottLawrence ShapiroFlorian KrammerPeter D KwongMark Connors
Published in: Science immunology (2020)
Induction of an antibody response capable of recognizing highly diverse strains is a major obstacle to the development of vaccines for viruses such as HIV and influenza. Here, we report the dynamics of B cell expansion and evolution at the single-cell level after vaccination with a replication-competent adenovirus type 4 recombinant virus expressing influenza H5 hemagglutinin. Fluorescent H1 or H5 probes were used to quantitate and isolate peripheral blood B cells and their antigen receptors. We observed increases in H5-specific antibody somatic hypermutation and potency for several months beyond the period of active viral replication that was not detectable at the serum level. Individual broad and potent antibodies could be isolated, including one stem-specific antibody that is part of a new multidonor class. These results demonstrate prolonged evolution of the B cell response for months after vaccination and should be considered in efforts to evaluate or boost vaccine-induced immunity.
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