BTLA is a lymphocyte inhibitory receptor with similarities to CTLA-4 and PD-1

被引:693
作者
Watanabe, N
Gavrieli, M
Sedy, JR
Yang, JF
Fallarino, F
Loftin, SK
Hurchla, MA
Zimmerman, N
Sim, J
Zang, XX
Murphy, TL
Russell, JH
Allison, JP
Murphy, KM
机构
[1] Washington Univ, Sch Med, Howard Hughes Med Inst, Dept Pathol & Immunol, St Louis, MO 63110 USA
[2] Univ Perugia, Dept Expt Med, I-06122 Perugia, Italy
[3] Washington Univ, Sch Med, Dept Mol Biol & Pharmacol, St Louis, MO 63110 USA
[4] Univ Calif Berkeley, Howard Hughes Med Inst, Dept Mol & Cell Biol, Canc Res Lab, Berkeley, CA 94720 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/ni944
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
During activation, T cells express receptors for receiving positive and negative costimulatory signals. Here we identify the B and T lymphocyte attenuator (BTLA), an immunoglobulin domain-containing glycoprotein with two immunoreceptor tyrosine-based inhibitory motifs. BTLA is not expressed by naive T cells, but it is induced during activation and remains expressed on T helper type 1 (T(H)1) but not T(H)2 cells. Crosslinking BTLA with antigen receptors induces its tyrosine phosphorylation and association with the Src homology domain 2 (SH2)-containing protein tyrosine phosphatases SHP-1 and SHP-2, and attenuates production of interleukin 2 (IL-2). BTLA-deficient T cells show increased proliferation, and BTLA-deficient mice have increased specific antibody responses and enhanced sensitivity to experimental autoimmune encephalomyelitis. B7x, a peripheral homolog of B7, is a ligand of BTLA. Thus, BTLA is a third inhibitory receptor on T lymphocytes with similarities to cytotoxic T lymphocyte-associated antigen 4 (CTLA-4) and programmed death 1 (PD-1).
引用
收藏
页码:670 / 679
页数:10
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