Molecular analysis of original antigenic sin. I. Clonal selection, somatic mutation, and isotype switching during a memory B cell response

TitleMolecular analysis of original antigenic sin. I. Clonal selection, somatic mutation, and isotype switching during a memory B cell response
Publication TypeJournal Article
Year of Publication1989
AuthorsFish, S., Zenowich E., Fleming M., & Manser T.
JournalThe Journal of experimental medicine
Volume170
Issue4
Pagination1191-209
Date Published1989 Oct 01
ISSN0022-1007
KeywordsAnimals; Antibody Specificity; Azo Compounds; B-Lymphocytes; Base Sequence; Benzenesulfonates; Clone Cells; Epitopes; Genes, Immunoglobulin; Genes, Switch; Hybridomas; Immunoglobulin Heavy Chains; Immunoglobulin Isotypes; Immunoglobulin kappa-Chains; Immunoglobulin Variable Region; Immunologic Memory; Mice; Mice, Inbred A; Molecular Sequence Data; Mutation; p-Azobenzenearsonate
Abstract

To determine how the memory B cell population elicited to one epitope might be used in immune responses to other, structurally related epitopes, we explored the phenomenon of original antigenic sin. Strain A/J mice reproducibly respond to immunization with p-azophenylarsonate (Ars) by production of anti-Ars antibodies encoded predominantly by a single VH gene segment (VHIdCR). The structural analogue of Ars p-azophenylsulfonate (Sulf) fails alone to elicit such V regions, but can do so in A/J mice previously immunized with Ars, providing a means to specifically examine B cells capable of responding secondarily to a crossreactive antigen (i.e., memory cells). VHIdCR-expressing hybridomas were derived from the Ars-primed, Sulf-boosted original antigenic sin response of A/J mice at various times after Ars priming, and the properties of the antibodies they express and the structure of the genes encoding these antibodies were characterized. The data obtained support the following conclusions: (a) The Ars-induced memory B cell population capable of being crossreactively stimulated by Sulf is largely formed from a small fraction of all B cells participating in the anti-Ars primary response that express somatically mutated V regions; (b) the antibody repertoire and clonal composition of this population are stable over long periods of time; (c) memory B cells are capable of clonal expansion in the absence of a high rate of V gene somatic mutation; (d) the activation requirements for clonal selection of memory, versus naive B cells appear to differ; and (e) a major fraction of Ars-induced memory B cells express either IgM or IgG3 prior to and during the initial stages of the sin response.

Alternate JournalJ. Exp. Med
Refereed DesignationRefereed