4.5 Article

Loss of CD8 and TCR binding to class I MHC ligands following T cell activation

期刊

INTERNATIONAL IMMUNOLOGY
卷 17, 期 12, 页码 1607-1617

出版社

OXFORD UNIV PRESS
DOI: 10.1093/intimm/dxh340

关键词

activation; CTL; tetramer

资金

  1. NIAID NIH HHS [AI52163, T32 AI007313] Funding Source: Medline

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The capacity of T cells to bind peptide/MHC ligands changes with T cell development and differentiation. Here we study changes in peptide/MHC multimer binding following T cell activation. Surprisingly, T cell activation caused a marked reduction in specific peptide/MHC Class I multimer binding, which was distinct from transient TCR down-regulation, and was especially dramatic for engagement with low-affinity peptide/MHC ligands. Direct CD8-Class I interactions were also profoundly and rapidly impaired following T cell stimulation, even though surface CD8 alpha and CD8 beta levels were unchanged after activation, suggesting that decreased CD8 co-receptor binding contributes to this effect. Finally, we show that enzymatic desialylation restores much of the multimer binding on activated T cells, suggesting that altered glycosylation may inhibit TCR/CD8 binding to peptide/MHC ligands. These radical changes in activated T cells' ability to perceive peptide/MHC ligands may contribute to selective outgrowth of clones with high affinity for the stimulatory ligand.

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