TY - JOUR
T1 - CD4+ regulatory T cells in autoimmunity and allergy
AU - Curotto de Lafaille, Maria A.
AU - Lafaille, Juan J.
N1 - Funding Information:
Work in our laboratory is supported by the National Institutes of Health, the National Multiple Sclerosis Society, and the Dana and Goldsmith Foundations.
PY - 2002/12/1
Y1 - 2002/12/1
N2 - Regulatory T cells (also referred to as suppressor T cells) are important components of the homeostasis of the immune system, as impaired regulatory T cell activity can cause autoimmune diseases and atopy. It is now clear that the phrase 'regulatory T cells' encompasses more than one cell type. For instance, CD4+CD25+ regulatory T cells have received attention due to their immunosuppressive properties in vitro and in vivo, but in several instances it has been shown that CD4+CD25- T cell populations also contain potent regulatory activity. Recent progress in the field of regulatory T cells includes the discovery of the role of two tumor necrosis factor receptor (TNFR) family members (GITR and TRANCE-R/RANK) in Treg biology, the improved understanding of the role of co-stimulatory molecules and cytokines IL-10 and IL-2 in the induction and function of Tregs, and the generation of CD25+ and CD25- regulatory T cells in vivo through high-avidity T cell receptor interactions.
AB - Regulatory T cells (also referred to as suppressor T cells) are important components of the homeostasis of the immune system, as impaired regulatory T cell activity can cause autoimmune diseases and atopy. It is now clear that the phrase 'regulatory T cells' encompasses more than one cell type. For instance, CD4+CD25+ regulatory T cells have received attention due to their immunosuppressive properties in vitro and in vivo, but in several instances it has been shown that CD4+CD25- T cell populations also contain potent regulatory activity. Recent progress in the field of regulatory T cells includes the discovery of the role of two tumor necrosis factor receptor (TNFR) family members (GITR and TRANCE-R/RANK) in Treg biology, the improved understanding of the role of co-stimulatory molecules and cytokines IL-10 and IL-2 in the induction and function of Tregs, and the generation of CD25+ and CD25- regulatory T cells in vivo through high-avidity T cell receptor interactions.
UR - http://www.scopus.com/inward/record.url?scp=0036888684&partnerID=8YFLogxK
U2 - 10.1016/S0952-7915(02)00408-9
DO - 10.1016/S0952-7915(02)00408-9
M3 - Review article
C2 - 12413528
AN - SCOPUS:0036888684
SN - 0952-7915
VL - 14
SP - 771
EP - 778
JO - Current Opinion in Immunology
JF - Current Opinion in Immunology
IS - 6
ER -