Enhanced suppressive function of regulatory T cells from patients with immune-mediated diseases following successful ex vivo expansion

被引:18
|
作者
Cao, Tinghua [1 ]
Wenzel, Sally E. [2 ]
Faubion, William A. [3 ]
Harriman, Gregory [1 ]
Li, Li [1 ]
机构
[1] Therakos Inc, Raritan, NJ 08869 USA
[2] Univ Pittsburgh, Med Ctr, Div Pulm Allergy & Crit Care Med, Pittsburgh, PA 15213 USA
[3] Mayo Clin, Dept Internal Med, Div Gastroenterol & Hepatol, Rochester, MN 55905 USA
关键词
Human; Treg cells; Expansion; Suppression; Immune-mediated disease; Severe asthma; SLE; RA; MS; CD; VERSUS-HOST-DISEASE; SYSTEMIC-LUPUS-ERYTHEMATOSUS; BONE-MARROW-TRANSPLANTATION; COLLAGEN-INDUCED ARTHRITIS; AUTOIMMUNE ENCEPHALOMYELITIS; RHEUMATOID-ARTHRITIS; MULTIPLE-SCLEROSIS; ADOPTIVE TRANSFER; CUTTING EDGE; EXPRESSION;
D O I
10.1016/j.clim.2010.04.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent studies and our current data demonstrated the deficits in the numbers and/or functions of the CD4(+)CD25(+)Foxp3(+) Treg cells in the patients with autoimmune diseases, indicating that restoration of Treg cells in these patients could be a potential therapeutic approach. Here, we demonstrated that CD4(+)CD25(+)Foxp3(+) Treg cells can be purified, activated and expanded from peripheral blood of patients with immune-mediated diseases, to a similar degree to those from healthy donors. Within 3 weeks, Treg cells from most patients could be expanded ex vivo 100-2000 fold and maintained their phenotypic characteristics. Furthermore, ex vivo expanded Treg cells displayed potent and enhanced in vitro suppressive activities inhibiting T effector cell proliferation compared to Treg cells freshly purified from the same patients. The expanded Treg cells with enhanced biological function may provide an opportunity to restore the proper balance of immunity and tolerance, suggesting the potential of using Treg cell therapy for treatment of immune-mediated diseases. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:329 / 337
页数:9
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