Molecules involved in T-B co-stimulation and B cell homeostasis: possible targets for an immunological intervention in autoimmunity

Expert Opin Biol Ther. 2005 Sep;5 Suppl 1:S61-71. doi: 10.1517/14712598.5.1.s61.

Abstract

The deepened knowledge of co-stimulatory mechanisms within the immunological synapse and the emerging biological principles governing B cell homeostasis provide a plethora of new possibilities to selectively block or enhance immune responses. These mechanisms are highly relevant to the development of new treatment modalities for autoimmune diseases. Here we review approaches to antagonise members of the CD28-B7 superfamily as well as the TNF receptor ligand superfamily members, BAFF and APRIL, and their corresponding receptors on B cells (BAFF-R, TACI and BCMA). The proof of principle that such manipulations have indeed profound consequences for the human immune response comes from genetically manipulated mouse models, and, more importantly, from human immunodeficiency syndromes. Thus, the recent discovery of deletions in the ICOS, BAFF-R and TACI genes leading to disturbances in late B cell differentiation and hypogammaglobulinaemia underline the potential impact of targeting these molecules for therapeutic strategies in autoimmune disorders.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antibodies, Monoclonal / pharmacology
  • Antibodies, Monoclonal / therapeutic use
  • Autoimmune Diseases / drug therapy
  • Autoimmune Diseases / metabolism
  • B-Lymphocytes / drug effects
  • B-Lymphocytes / metabolism
  • B7-1 Antigen / immunology
  • B7-1 Antigen / metabolism
  • CD28 Antigens / immunology
  • CD28 Antigens / metabolism
  • Cell Communication
  • Cell Differentiation
  • Common Variable Immunodeficiency / drug therapy
  • Common Variable Immunodeficiency / metabolism
  • Humans
  • Receptors, Tumor Necrosis Factor / antagonists & inhibitors
  • Receptors, Tumor Necrosis Factor / immunology
  • Receptors, Tumor Necrosis Factor / metabolism
  • Recombinant Fusion Proteins / pharmacology
  • Recombinant Fusion Proteins / therapeutic use
  • Signal Transduction
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / metabolism*
  • Tumor Necrosis Factor Inhibitors
  • Tumor Necrosis Factors / immunology
  • Tumor Necrosis Factors / metabolism

Substances

  • Antibodies, Monoclonal
  • B7-1 Antigen
  • CD28 Antigens
  • Receptors, Tumor Necrosis Factor
  • Recombinant Fusion Proteins
  • Tumor Necrosis Factor Inhibitors
  • Tumor Necrosis Factors