Antibody Affinity Shapes the Choice Between Memory and Germinal Center B Cell Fates

Overview

Journal Cell

Publisher Cell Press

Specialty Cell Biology

Date 2020 Oct 30

PMID 33125897

Citations 103

Authors

Charlotte Viant

Georg H J Weymar

Amelia Escolano

Spencer Chen

Harald Hartweger

Melissa Cipolla

Anna Gazumyan

Michel C Nussenzweig

Affiliations

Soon will be listed here.

Abstract

Immunological memory is required for protection against repeated infections and is the basis of all effective vaccines. Antibodies produced by memory B cells play an essential role in many of these responses. We have combined lineage tracing with antibody cloning from single B cells to examine the role of affinity in B cell selection into germinal centers (GCs) and the memory B cell compartment in mice immunized with an HIV-1 antigen. We find that contemporaneously developing memory and GC B cells differ in their affinity for antigen throughout the immune response. Whereas GC cells and their precursors are enriched in antigen binding, memory B cells are not. Thus, the polyclonal memory B cell compartment is composed of B cells that were activated during the immune response but whose antigen binding affinity failed to support further clonal expansion in the GC.

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