Peripheral tolerance is mediated by multiple mechanisms such as anergy and/or active suppression of effector T cells by T regulatory (Tr) cells. Among the CD4(+) Tr cells, T regulatory type 1 cells (Tr1) have been shown to down-modulate immune responses through production of the immunosuppressive cytokines IL-10 and TGF-beta. Tr1 cells maintain peripheral tolerance, control autoimmumity, and prevent allograft rejection and graft versus host disease (GvHD). Cellular therapy with ex vivo generated Trl cells has been proven to be effective in several preclinical models of T cell-mediated pathologies and therefore, represents a promising approach for clinical application. This review will summarize the new findings on TO cells, the recent development of methods for their ex vivo expansion, and their potential clinical relevance as cellular therapy. (c) 2006 Elsevier Ltd. All rights reserved.
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Ann & Robert H Lurie Childrens Hosp Chicago, Chicago, IL 60611 USA
Ann & Robert H Lurie Childrens Hosp Chicago, Dept Pediat, Div Allergy Immunol, Chicago, IL 60611 USAAnn & Robert H Lurie Childrens Hosp Chicago, Chicago, IL 60611 USA
Bergerson, Jenna R.
Erickson, Kristin A.
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Northwestern Univ, Dept Pediat, Feinberg Sch Med, Div Allergy Immunol, Chicago, IL 60611 USAAnn & Robert H Lurie Childrens Hosp Chicago, Chicago, IL 60611 USA
Erickson, Kristin A.
Singh, Anne Marie
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Ann & Robert H Lurie Childrens Hosp Chicago, Dept Pediat, Div Allergy Immunol, Chicago, IL 60611 USA
Northwestern Univ, Dept Pediat, Ann & Robert H Lurie Childrens Hosp Chicago, Div Allergy & Immunol,Feinberg Sch Med, Chicago, IL 60611 USAAnn & Robert H Lurie Childrens Hosp Chicago, Chicago, IL 60611 USA