Frontiers in Immunology (Jan 2019)

Insights From Analysis of Human Antigen-Specific Memory B Cell Repertoires

  • Hemangi B. Shah,
  • Kenneth Smith,
  • Jonathan D. Wren,
  • Jonathan D. Wren,
  • Carol F. Webb,
  • Carol F. Webb,
  • Jimmy D. Ballard,
  • Rebecka L. Bourn,
  • Judith A. James,
  • Judith A. James,
  • Mark L. Lang

DOI
https://doi.org/10.3389/fimmu.2018.03064
Journal volume & issue
Vol. 9

Abstract

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Memory B cells that are generated during an infection or following vaccination act as sentinels to guard against future infections. Upon repeat antigen exposure memory B cells differentiate into new antibody-secreting plasma cells to provide rapid and sustained protection. Some pathogens evade or suppress the humoral immune system, or induce memory B cells with a diminished ability to differentiate into new plasma cells. This leaves the host vulnerable to chronic or recurrent infections. Single cell approaches coupled with next generation antibody gene sequencing facilitate a detailed analysis of the pathogen-specific memory B cell repertoire. Monoclonal antibodies that are generated from antibody gene sequences allow a functional analysis of the repertoire. This review discusses what has been learned thus far from analysis of diverse pathogen-specific memory B cell compartments and describes major differences in their repertoires. Such information may illuminate ways to advance the goal of improving vaccine and therapeutic antibody design.

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