Disturbed B-lymphocyte selection in autoimmune lymphoproliferative syndrome

Blood. 2016 May 5;127(18):2193-202. doi: 10.1182/blood-2015-04-642488. Epub 2016 Feb 23.

Abstract

Fas is a transmembrane receptor involved in the maintenance of tolerance and immune homeostasis. In murine models, it has been shown to be essential for deletion of autoreactive B cells in the germinal center. The role of Fas in human B-cell selection and in development of autoimmunity in patients carrying FAS mutations is unclear. We analyzed patients with either a somatic FAS mutation or a germline FAS mutation and somatic loss-of-heterozygosity, which allows comparing the fate of B cells with impaired vs normal Fas signaling within the same individual. Class-switched memory B cells showed: accumulation of FAS-mutated B cells; failure to enrich single V, D, J genes and single V-D, D-J gene combinations of the B-cell receptor variable region; increased frequency of variable regions with higher content of positively charged amino acids; and longer CDR3 and maintenance of polyreactive specificities. Importantly, Fas-deficient switched memory B cells showed increased rates of somatic hypermutation. Our data uncover a defect in B-cell selection in patients with FAS mutations, which has implications for the understanding of the pathogenesis of autoimmunity and lymphomagenesis of autoimmune lymphoproliferative syndrome.

Keywords: ALPS and B cells; ALPS and B-lymphocytes; ALPS and Rizzi; autoimmune lymphoproliferative syndrome and B cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Apoptosis
  • Autoimmune Lymphoproliferative Syndrome / immunology*
  • Autoimmunity
  • B-Lymphocyte Subsets / immunology*
  • Cell Line, Transformed
  • Cell Transformation, Neoplastic
  • Child
  • Clonal Selection, Antigen-Mediated*
  • Codon, Nonsense
  • Female
  • Frameshift Mutation
  • Germ-Line Mutation
  • Heterozygote
  • Humans
  • Immunologic Memory
  • Loss of Heterozygosity
  • Male
  • Mutation*
  • Sequence Analysis, DNA
  • Somatic Hypermutation, Immunoglobulin
  • V(D)J Recombination
  • fas Receptor / deficiency
  • fas Receptor / genetics
  • fas Receptor / physiology*

Substances

  • Codon, Nonsense
  • FAS protein, human
  • fas Receptor