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TREM-1 (triggering receptor expressed on myeloid cells): A new player in acute inflammatory responses
被引:234
作者:

Colonna, M
论文数: 0 引用数: 0
h-index: 0
机构: Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA

Facchetti, F
论文数: 0 引用数: 0
h-index: 0
机构: Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
机构:
[1] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
[2] Univ Brescia, Dept Pathol, Brescia, Italy
关键词:
D O I:
10.1086/374754
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
TREM-1 (triggering receptor expressed on myeloid cells), a recently discovered receptor of the immunoglobulin superfamily, activates neutrophils and monocytes/macrophages by signaling through the adapter protein DAP12. TREM-1 is the best-characterized member of a growing family of DAP12-associated receptors that regulate the function of myeloid cells in innate and adaptive responses. TREM-1 amplifies Toll-like receptor-initiated responses against microbial challenges and potentiates the secretion of proinflammatory chemokines and cytokines in response to bacterial and fungal infections. Blockade of TREM-1 reduces inflammation and increases survival in animal models of bacterial infections that cause systemic hyperinflammatory syndromes. The TREM-1 ligands are not known. Characterization of TREM-1 natural ligands will further illuminate the mechanisms regulating innate responses against pathogens. Whatever the ligands, targeted activation or blockade of TREM-1 and its ligands may help maximize the efficacy of existing treatments for sepsis.
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页码:S397 / S401
页数:5
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