Galectin-9 binding to Tim-3 renders activated human CD4+ T cells less susceptible to HIV-1 infection

被引:106
作者
Elahi, Shokrollah [1 ]
Niki, Toshiro [2 ,3 ]
Hirashima, Mitsuomi [2 ,3 ]
Horton, Helen [1 ,4 ,5 ]
机构
[1] Seattle Biomed Res Inst Seattle Biomed, Viral Vaccine Program, Seattle, WA USA
[2] Kagawa Univ, Dept Immunol & Immunopathol, Takamatsu, Kagawa 760, Japan
[3] Galpharma, Res Ctr, Takamatsu, Kagawa, Japan
[4] Univ Washington, Dept Med, Seattle, WA USA
[5] Univ Washington, Dept Global Hlth Med, Seattle, WA USA
基金
美国国家卫生研究院;
关键词
EOSINOPHIL CHEMOATTRACTANT; EXPRESSION; SUPPRESSES; RESISTANCE; INHIBITION; IMMUNOLOGY; MIGRATION; EPITOPES; IMMUNITY; DEFINES;
D O I
10.1182/blood-2011-11-389585
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Galectin-9 (Gal-9) is a tandem repeat-type member of the galectin family and is a ligand for T-cell immunoglobulin mucin domain 3 (Tim-3), a type-I glycoprotein that is persistently expressed on dysfunctional T cells during chronic infection. Studies in autoimmune diseases and chronic viral infections show that Tim-3 is a regulatory molecule that inhibits Th1 type immune responses. Here we show that soluble Gal-9 interacts with Tim-3 expressed on the surface of activated CD4(+) T cells and renders them less susceptible to HIV-1 infection and replication. The Gal-9/Tim-3 interaction on activated CD4(+) T cells, leads to down-regulation of HIV-1 coreceptors and up-regulation of the cyclin-dependent kinase inhibitor p21 (also known as cip-1 and waf-1). We suggest that higher expression of Tim-3 during chronic infection has evolved to limit persistent immune activation and associated tissue damage. These data demonstrate a novel mechanism for Gal-9/Tim-3 interactions to induce resistance of activated CD4(+) T cells to HIV-1 infection and suggest that Gal-9 may play a role in HIV-1 pathogenesis and could be used as a novel microbicide to prevent HIV-1 infection. (Blood. 2012;119(18):4192-4204)
引用
收藏
页码:4192 / 4204
页数:13
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