Early precursors and molecular determinants of tissue-resident memory CD8+ T lymphocytes revealed by single-cell RNA sequencing

被引:128
|
作者
Kurd, Nadia S. [1 ,6 ]
He, Zhaoren [2 ,3 ]
Louis, Tiani L. [1 ]
Milner, J. Justin [3 ]
Omilusik, Kyla D. [3 ]
Jin, Wenhao [2 ]
Tsai, Matthew S. [1 ]
Widjaja, Christella E. [1 ]
Kanbar, Jad N. [1 ]
Olvera, Jocelyn G. [1 ]
Tysl, Tiffani [1 ]
Quezada, Lauren K. [1 ]
Boland, Brigid S. [1 ]
Huang, Wendy J. [2 ]
Murre, Cornelis [3 ]
Goldrath, Ananda W. [3 ]
Yeo, Gene W. [2 ,4 ]
Chang, John T. [1 ,5 ]
机构
[1] Univ Calif San Diego, Dept Med, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Dept Cellular & Mol Med, La Jolla, CA 92093 USA
[3] Univ Calif San Diego, Div Biol Sci, La Jolla, CA 92093 USA
[4] Univ Calif San Diego, Inst Genom Med, La Jolla, CA 92093 USA
[5] VA San Diego Healthcare Syst, Div Gastroenterol, San Diego, CA 92161 USA
[6] Pfizer Oncol Res & Dev, Canc Immunol Discovery, La Jolla, CA 92121 USA
关键词
TERMINAL DIFFERENTIATION; NONLYMPHOID TISSUES; EFFECTOR; EXPRESSION; SUBSETS; PERSISTENCE; REPRESSION; IMMUNITY; TRIGGER; STAGE;
D O I
10.1126/sciimmunol.aaz6894
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
During an immune response to microbial infection, CD8(+) T cells give rise to distinct classes of cellular progeny that coordinately mediate clearance of the pathogen and provide long-lasting protection against reinfection, including a subset of noncirculating tissue-resident memory (TRM) cells that mediate potent protection within nonlymphoid tissues. Here, we used single-cell RNA sequencing to examine the gene expression patterns of individual CD8(+) T cells in the spleen and small intestine intraepithelial lymphocyte (siIEL) compartment throughout the course of their differentiation in response to viral infection. These analyses revealed previously unknown transcriptional heterogeneity within the siIEL CD8(+) T cell population at several stages of differentiation, representing functionally distinct TRM cell subsets and a subset of TRM cell precursors within the tissue early in infection. Together, these findings may inform strategies to optimize CD8(+) T cell responses to protect against microbial infection and cancer.
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收藏
页数:16
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