4.6 Article

Cutting Edge: Mincle Is Essential for Recognition and Adjuvanticity of the Mycobacterial Cord Factor and its Synthetic Analog Trehalose-Dibehenate

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JOURNAL OF IMMUNOLOGY
卷 184, 期 6, 页码 2756-2760

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AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.0904013

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资金

  1. Deutsche Forschungsgemeinschaft [SFB796, TP B6, SFB576, SFB643, FOR832]
  2. European Union [LSHP-CT-2003-503367]
  3. Deutsche Krebshilfe
  4. Wellcome Trust
  5. National Health and Medical Research Council, Australia [455947, 597452, 481945]

向作者/读者索取更多资源

The mycobacterial cord factor trehalose-6,6-dimycolate (TDM) and its synthetic analog trehalose-6,6-dibehenate (TDB) are potent adjuvants for Th1/Th17 vaccination that activate Syk-Card9 signaling in APCs. In this study, we have further investigated the molecular mechanism of innate immune activation by TDM and TDB. The Syk-coupling adapter protein FcR gamma was essential for macrophage activation and Th17 adjuvanticity. The FcR gamma-associated C-type lectin receptor Mincle was expressed in macrophages and upregulated by TDM and TDB. Recombinant Mincle-Fc fusion protein specifically bound to the glycolipids. Genetic ablation or Mincle abolished TDM/TDB-induced macrophage activation and induction of T cell immune responses to a tuberculosis subunit vaccine. Macrophages lacking Mincle or FcR gamma were impaired in the inflammatory response to Mycobacterium bovis bacillus Calmette-Guerin. These results establish that Mincle is a key receptor for the mycobacterial cord factor and controls the Th1/Th17 adjuvanticity of TDM and TDB. The Journal of Immunology, 2010, 184: 2756-2760.

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