Mitochondria-dependent apoptosis in T-cell homeostasis

Curr Opin Investig Drugs. 2005 Nov;6(11):1095-102.

Abstract

T-cell homeostasis is maintained by balancing the proliferation and destruction of lymphocytes at multiple steps during the life of an individual. Regulated mitochondria-dependent apoptosis is essential for both the development and the subsequent maintenance of the immune system, in that it keeps the total number of lymphocytes constant. Firstly, during thymic development, sequential stages of T-cell maturation require strict control of T-cell selection, and secondly, apoptosis is essential in controlling the massive expansion of antigen-specific T-cells after their activation. Failure in each of these steps can lead to pathologies, while drugs that target apoptosis could have therapeutic benefit.

Publication types

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

MeSH terms

  • Animals
  • Antiviral Agents / therapeutic use
  • Apoptosis / drug effects
  • Apoptosis / immunology*
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / therapy*
  • Benzamides
  • Clonal Deletion
  • HIV Infections / immunology
  • HIV Infections / therapy
  • Homeostasis / immunology*
  • Humans
  • Imatinib Mesylate
  • Immunotherapy, Active*
  • Leukemia / drug therapy
  • Leukemia / immunology
  • Leukemia / metabolism
  • Lymphocyte Activation
  • Mitochondria / drug effects
  • Mitochondria / immunology*
  • Mitochondria / metabolism
  • Piperazines / therapeutic use
  • Protein Kinase Inhibitors / therapeutic use
  • Pyrimidines / therapeutic use
  • Signal Transduction / drug effects
  • Signal Transduction / immunology
  • T-Lymphocytes / drug effects
  • T-Lymphocytes / immunology*
  • T-Lymphocytes / metabolism
  • Thymus Gland / cytology
  • Thymus Gland / immunology

Substances

  • Antiviral Agents
  • Benzamides
  • Piperazines
  • Protein Kinase Inhibitors
  • Pyrimidines
  • Imatinib Mesylate