Low-Dose IL-2 for In Vivo Expansion of CD4+ and CD8+ Regulatory T Cells in Nonhuman Primates

被引:24
作者
Aoyama, A. [1 ]
Klarin, D. [1 ]
Yamada, Y. [1 ]
Boskovic, S. [1 ]
Nadazdin, O. [1 ]
Kawai, K. [1 ]
Schoenfeld, D. [2 ]
Madsen, J. C. [1 ]
Cosimi, A. B. [1 ]
Benichou, G. [1 ]
Kawai, T. [1 ]
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Transplant Ctr, Boston, MA 02115 USA
[2] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Biostat, Boston, MA USA
关键词
Immunotherapy; interleukin-2; nonhuman primates; T-regulatory cells; INTERLEUKIN-2; THERAPY; HIV-INFECTION; TOLERANCE; DISEASES;
D O I
10.1111/j.1600-6143.2012.04133.x
中图分类号
R61 [外科手术学];
学科分类号
摘要
IL-2 is a known potent T cell growth factor that amplifies lymphocyte responses in vivo. This capacity has led to the use of high-dose IL-2 to enhance T cell immunity in patients with AIDS or cancer. However, more recent studies have indicated that IL-2 is also critical for the development and peripheral expansion of regulatory T cells (Tregs). In the current study, low-dose IL-2 (1 million IU/m2 BSA/day) was administered to expand Tregs in vivo in naive nonhuman primates. Our study demonstrated that low-dose IL-2 therapy significantly expanded peripheral blood CD4+ and CD8+ Tregs in vivo with limited expansion of non-Treg cells. These expanded Tregs are mainly CD45RA- Foxp3 high activated Tregs and demonstrated potent immunosuppressive function in vitro. The results of this preclinical study can serve as a basis to develop Treg immunotherapy, which has significant therapeutic potential in organ/cellular transplantation.
引用
收藏
页码:2532 / 2537
页数:6
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