4.6 Article

Cutting Edge: Resident Memory CD8 T Cells Express High-Affinity TCRs

期刊

JOURNAL OF IMMUNOLOGY
卷 195, 期 8, 页码 3520-3524

出版社

AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1501521

关键词

-

资金

  1. PML Consortium, LLC
  2. National Institutes of Health [R01 NS088367, R01 AI102543, T32 AI007610, F31 NS083336, R01 AI096879, NS071518, F31 NS081828]

向作者/读者索取更多资源

Tissue-resident memory T (T-RM) cells serve as vanguards of antimicrobial host defense in nonlymphoid tissues, particularly at barrier epithelia and in organs with nonrenewable cell types (e.g., brain). In this study, we asked whether an augmented ability to sense Ag complemented their role as early alarms of pathogen invasion. Using mouse polyomavirus, we show that brain-resident mouse polyomavirus-specific CD8 T cells, unlike memory cells in the spleen, progressively increase binding to MHC class I tetramers and CD8 coreceptor expression. Using the two-dimensional micropipette adhesion-frequency assay, we show that TRM cells in brain, as well as in kidney, express TCRs with up to 20-fold higher affinity than do splenic memory T cells, whereas effector cells express TCRs of similar high affinity in all organs. Together, these data demonstrate that TRM cells retain high TCR affinity, which endows them with the high Ag sensitivity needed for front-line defense against infectious agents.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据