B cell-targeted therapies in Sjögren's syndrome

Autoimmun Rev. 2010 Feb;9(4):224-8. doi: 10.1016/j.autrev.2009.08.001. Epub 2009 Aug 9.

Abstract

Sjögren's syndrome (SS) or autoimmune epithelitis is characterized by focal lymphocytic infiltrates surrounding the tubular epithelium of exocrine glands and by overactivity of the B-cell population. Although T cells were long considered the main effectors in SS, recent findings indicating a key role for B cells have prompted studies of treatments designed to deplete the B-cell population. Among molecules that can be targeted to achieve B-cell depletion, CD20 and CD22 are surface antigens expressed specifically by B lymphocytes; and the cytokine B-cell-activating factor belonging to the TNF family (BAFF) is a TNF receptor ligand involved in B-cell differentiation, survival, and activation. The aim of this review is to discuss the clinical outcomes of SS patients treated with B-cell depletion.

Publication types

  • Review

MeSH terms

  • Antibodies, Monoclonal / pharmacology
  • Antibodies, Monoclonal / therapeutic use*
  • Antigens, CD20 / immunology
  • B-Cell Activating Factor / immunology
  • B-Lymphocytes / drug effects
  • B-Lymphocytes / immunology*
  • B-Lymphocytes / metabolism
  • Cell Differentiation / drug effects
  • Cell Proliferation / drug effects
  • Humans
  • Immunotherapy*
  • Lymphocyte Activation / drug effects
  • Lymphocyte Depletion
  • Protein Engineering
  • Randomized Controlled Trials as Topic
  • Recombinant Fusion Proteins / pharmacology
  • Recombinant Fusion Proteins / therapeutic use*
  • Sialic Acid Binding Ig-like Lectin 2 / immunology
  • Sjogren's Syndrome / immunology*
  • Sjogren's Syndrome / therapy

Substances

  • Antibodies, Monoclonal
  • Antigens, CD20
  • B-Cell Activating Factor
  • Recombinant Fusion Proteins
  • Sialic Acid Binding Ig-like Lectin 2
  • TNFSF13B protein, human