| Literature DB >> 29343437 |
Kevin R McCarthy1, Akiko Watanabe2, Masayuki Kuraoka2, Khoi T Do1, Charles E McGee3, Gregory D Sempowski3, Thomas B Kepler4, Aaron G Schmidt1, Garnett Kelsoe5, Stephen C Harrison6.
Abstract
Human B cell antigen-receptor (BCR) repertoires reflect repeated exposures to evolving influenza viruses; new exposures update the previously generated B cell memory (Bmem) population. Despite structural similarity of hemagglutinins (HAs) from the two groups of influenza A viruses, cross-reacting antibodies (Abs) are uncommon. We analyzed Bmem compartments in three unrelated, adult donors and found frequent cross-group BCRs, both HA-head directed and non-head directed. Members of a clonal lineage from one donor had a BCR structure similar to that of a previously described Ab, encoded by different gene segments. Comparison showed that both Abs contacted the HA receptor-binding site through long heavy-chain third complementarity determining regions. Affinities of the clonal-lineage BCRs for historical influenza-virus HAs from both group 1 and group 2 viruses suggested that serial responses to seasonal influenza exposures had elicited the lineage and driven affinity maturation. We propose that appropriate immunization regimens might elicit a comparably broad response.Entities:
Keywords: B cell repertoire; clonal selection; convergent evolution; influenza hemagglutinin
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Year: 2018 PMID: 29343437 PMCID: PMC5810956 DOI: 10.1016/j.immuni.2017.12.009
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 43.474