The Fas/CD95 receptor regulates the death of autoreactive B cells and the selection of antigen-specific B cells

G. Koncz, Anne Odile Hueber

Research output: Article

29 Citations (Scopus)

Abstract

Cell death receptors have crucial roles in the regulation of immune responses. Here we review recent in vivo data confirming that the Fas death receptor (TNFSR6) on B cells is important for the regulation of autoimmunity since the impairment of only Fas function on B cells results in uncontrolled autoantibody production and autoimmunity. Fas plays a role in the elimination of the non-specific and autoreactive B cells in germinal center, while during the selection of antigen-specific B cells different escape signals ensure the resistance to Fas-mediated apoptosis. Antigen-specific survival such as BCR or MHCII signal or coreceptors (CD19) cooperating with BCR inhibits the formation of death inducing signaling complex. Antigen-specific survival can be reinforced by antigen-independent signals of IL-4 or CD40 overproducing the anti-apoptotic members of the Bcl-2 family proteins.

Original languageEnglish
Article numberArticle 207
JournalFrontiers in Immunology
Volume3
Issue numberJUL
DOIs
Publication statusPublished - 2012

Fingerprint

CD95 Antigens
B-Lymphocytes
Antigens
Death Domain Receptors
Autoimmunity
Death Domain Receptor Signaling Adaptor Proteins
Germinal Center
Interleukin-4
Autoantibodies
Cell Death
Apoptosis
Proteins

ASJC Scopus subject areas

  • Immunology
  • Immunology and Allergy

Cite this

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