Naive Human T Cells Are Activated and Proliferate in Response to the Heme Oxygenase-1 Inhibitor Tin Mesoporphyrin

被引:31
作者
Burt, Trevor D. [1 ,2 ]
Seu, Lillian [2 ,3 ]
Mold, Jeffrey E. [2 ]
Kappas, Attallah [5 ]
McCune, Joseph M. [2 ,4 ]
机构
[1] Univ Calif San Francisco, Div Neonatol, Dept Pediat, San Francisco, CA 94110 USA
[2] Univ Calif San Francisco, Dept Med, Div Expt Med, San Francisco Gen Hosp, San Francisco, CA 94110 USA
[3] Univ Calif San Francisco, Dept Bioengn & Therapeut Sci, San Francisco, CA 94110 USA
[4] Univ Calif San Francisco, Dept Microbiol & Immunol, San Francisco, CA 94110 USA
[5] Rockefeller Univ, Rockefeller Univ Hosp, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
ANTIGEN-PRESENTING CELLS; CARBON-MONOXIDE SUPPRESS; OXIDATIVE STRESS; HOMEOSTATIC PROLIFERATION; IN-VIVO; EXPRESSION; TOLERANCE; PROTEIN; INDUCTION; MOUSE;
D O I
10.4049/jimmunol.0903127
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Heme oxygenase-1 (HO-1) and its catabolic by-products have potent anti-inflammatory activity in many models of disease. It is not known, however, if HO-1 also plays a role in the homeostatic control of T cell activation and proliferation. We demonstrate here that the HO-1 inhibitor tin mesoporphyrin (SnMP) induces activation, proliferation, and maturation of naive CD4(+) and CD8(+) T cells via interactions with CD14(+) monocytes in vitro. This response is dependent upon interactions of T cells with MHC class I and II on the surface of CD14(+) monocytes. Furthermore, CD4(+)CD25(+)FoxP3(+) regulatory T cells were able to suppress this proliferation, even though their suppressive activity was itself impaired by SnMP. Given the magnitude of the Ag-independent T cell response induced by SnMP, we speculate that HO-1 plays an important role in dampening nonspecific T cell activation. Based on these findings, we propose a potential role for HO-1 in the control of naive T cell homeostatic proliferation. The Journal of Immunology, 2010, 185: 5279-5288.
引用
收藏
页码:5279 / 5288
页数:10
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