The regulatory T cell family : distinct subsets and their interrelations
Journal of immunology. Bd. 171. H. 12. Bethesda, Md.: American Assoc. of Immunologists 2003 S. 6323 - 6327
Erscheinungsjahr: 2003
ISBN/ISSN: 0022-1767
Publikationstyp: Zeitschriftenaufsatz
Sprache: Englisch
| Geprüft: | Bibliothek |
Inhaltszusammenfassung
The immune system, a highly effective and dynamic cellular network, protects a host from pathogens. Therefore, the immune system must distinguish self from nonself structures, but also between harmful and innocuous foreign Ags to prevent nonessential and self-destructive immune responses. The induction of Ag-specific T cell tolerance and its maintenance in the periphery are critical to prevent autoaggressive immune responses. A still growing body of evidence reveals that specific T ce...The immune system, a highly effective and dynamic cellular network, protects a host from pathogens. Therefore, the immune system must distinguish self from nonself structures, but also between harmful and innocuous foreign Ags to prevent nonessential and self-destructive immune responses. The induction of Ag-specific T cell tolerance and its maintenance in the periphery are critical to prevent autoaggressive immune responses. A still growing body of evidence reveals that specific T cell populations that have suppressive/ regulatory properties tightly control autoaggressive immune responses. Among the CD4 regulatory T cells (Tregs)3 basically two different subsets of Tregs can be differentiated by their distinct suppressive mechanisms. Naturally occurring CD4CD25 Tregs exert their suppressive effects obviously via cell contact by membrane-bound molecules although the nature of these molecules is still elusive. The suppressive capacity of the second subset, Th3 and type 1 T regulatory (Tr1) cells, is contact independent and is based mainly on cytokines such as IL-10 and TGF-. It seems that these cells, in contrast to naturally occurring CD4CD25 Tregs, represent altered states of differentiation rather than a unique cell lineage. However, the interrelationship of these distinct subsets of CD4 Tregs is currently a matter of debate.» weiterlesen» einklappen
Autoren
Klassifikation
DFG Fachgebiet:
2.21 - Mikrobiologie, Virologie und Immunologie
DDC Sachgruppe:
Medizin