Somatic diversification of the B cell repertoire requires two cell subsets

Scand J Immunol. 2018 Mar;87(3). doi: 10.1111/sji.12640. Epub 2018 Jan 22.

Abstract

Evolution found itself in a Catch-22 situation when selecting for the somatically derived paratopic repertoire of the humoral immune system. The B cell BCR repertoire can only be somatically diversified from a substrate of paratopes that is encoded in the germline. In order for the cells expressing that substrate to also be a target of germline selection, their BCRs must, independently, be of selective value by being expressed in a functionally important way in each individual. A somatically derived repertoire scrambles this substrate so that its specificities are lost, making it unselectable in the germline. Consequently, evolution faced an incompatibility. Here, we explore what it takes to resolve it.

Keywords: B cell subsets; BCR; evolution; paratopic repertoire.

MeSH terms

  • Antibodies / immunology
  • B-Lymphocyte Subsets / cytology*
  • B-Lymphocyte Subsets / immunology
  • Binding Sites, Antibody / immunology*
  • Cell Differentiation / immunology*
  • Cell Lineage / immunology
  • Genes, Immunoglobulin
  • Humans
  • Immunity, Humoral / immunology
  • Immunoglobulin Variable Region / genetics
  • Immunoglobulin Variable Region / immunology*
  • Single-Domain Antibodies / genetics
  • Single-Domain Antibodies / immunology*

Substances

  • Antibodies
  • Immunoglobulin Variable Region
  • Single-Domain Antibodies