T cell costimulation by CD28, CTLA-4, and ICOS.
- Author:
Kyung Mi LEE
1
Author Information
- Publication Type:Review
- MeSH: Antigen-Presenting Cells; Biology; Receptors, Antigen, T-Cell; T-Lymphocytes
- From:Immune Network 2001;1(2):95-103
- CountryRepublic of Korea
- Language:Korean
- Abstract: T cells play a central role in the initiation and regulation of the immune response to foreign antigens. Full activation of T cells requires the engagement of T cell receptor complex (TCR) and the binding of a second costimulatory receptor to its ligand expressed on antigen presenting cells (APC). Among the molecules known to provide costimulatory function, CD28 has been the most dominant and potent costimulatory molecule. However, the function of CD28 is becoming more complex due to the recent discovery of its structural homologue, CTLA-4 and ICOS. This review summarizes the biology and physiologic function of each of these receptors, and further focuses on the biochemical mechanism underlying the function of these receptors. Complete understanding of the CD28/CTLA-4/ICOS costimulatory pathway will provide the basis for developing new therapeutic approaches for immunological dieseases.
