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Origin and differentiation of human memory CD8 T cells after vaccination.接种疫苗后人类记忆性 CD8 T 细胞的起源与分化。
Nature. 2017 Dec 21;552(7685):362-367. doi: 10.1038/nature24633. Epub 2017 Dec 13.
2
Effector CD8 T cells dedifferentiate into long-lived memory cells.效应性 CD8 T 细胞去分化为长寿命记忆细胞。
Nature. 2017 Dec 21;552(7685):404-409. doi: 10.1038/nature25144. Epub 2017 Dec 13.
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Runx3 programs CD8 T cell residency in non-lymphoid tissues and tumours.Runx3调控CD8 T细胞在非淋巴组织和肿瘤中的驻留。
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Mitochondrial Priming by CD28.CD28介导的线粒体启动
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Dynamics of influenza-induced lung-resident memory T cells underlie waning heterosubtypic immunity.流感诱导的肺驻留记忆T细胞动态变化是异源亚型免疫力下降的基础。
Sci Immunol. 2017 Jan 6;2(7). doi: 10.1126/sciimmunol.aag2031.
6
Resident memory T cells in the skin mediate durable immunity to melanoma.皮肤中的驻留记忆T细胞介导对黑色素瘤的持久免疫。
Sci Immunol. 2017 Apr 14;2(10). doi: 10.1126/sciimmunol.aam6346.
7
Chromatin states define tumour-specific T cell dysfunction and reprogramming.染色质状态决定肿瘤特异性T细胞功能障碍和重编程。
Nature. 2017 May 25;545(7655):452-456. doi: 10.1038/nature22367. Epub 2017 May 17.
8
Antigen-inexperienced memory CD8 T cells: where they come from and why we need them.未接触过抗原的记忆性CD8 T细胞:它们的来源及我们需要它们的原因。
Nat Rev Immunol. 2017 Jun;17(6):391-400. doi: 10.1038/nri.2017.34. Epub 2017 May 8.
9
Skin-resident CD4+ T cells protect against Leishmania major by recruiting and activating inflammatory monocytes.驻留皮肤的CD4+ T细胞通过招募和激活炎性单核细胞来抵御硕大利什曼原虫。
PLoS Pathog. 2017 Apr 18;13(4):e1006349. doi: 10.1371/journal.ppat.1006349. eCollection 2017 Apr.
10
Epigenetic landscapes reveal transcription factors that regulate CD8 T cell differentiation.表观遗传景观揭示了调节CD8 T细胞分化的转录因子。
Nat Immunol. 2017 May;18(5):573-582. doi: 10.1038/ni.3706. Epub 2017 Mar 13.

理解 T 细胞记忆中的亚群多样性。

Understanding Subset Diversity in T Cell Memory.

机构信息

Center for Immunology, Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN 55414, USA.

Department of Microbiology and Immunology, University of Minnesota, Minneapolis, MN 55414, USA.

出版信息

Immunity. 2018 Feb 20;48(2):214-226. doi: 10.1016/j.immuni.2018.02.010.

DOI:10.1016/j.immuni.2018.02.010
PMID:29466754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5863745/
Abstract

Considerable advances have been made in recent years in understanding the generation and function of memory T cells. Memory T cells are typically parsed into discreet subsets based on phenotypic definitions that connote distinct roles in immunity. Here we consider new developments in the field and focus on how emerging differences between memory cells with respect to their trafficking, metabolism, epigenetic regulation, and longevity may fail to fit into small groups of "memory subsets." Rather, the properties of individual memory T cells fall on a continuum within each of these and other parameters. We discuss how this continuum influences the way that the efficacy of vaccination is assessed, as well as the suitability of a memory population for protective immunity.

摘要

近年来,人们在理解记忆 T 细胞的产生和功能方面取得了重大进展。记忆 T 细胞通常根据表型定义划分为离散的亚群,这些定义暗示了它们在免疫中的不同作用。在这里,我们考虑该领域的新进展,并重点关注记忆细胞在其迁移、代谢、表观遗传调控和寿命方面的新兴差异如何无法归入少数“记忆亚群”。相反,单个记忆 T 细胞的特性在这些和其他参数中的每一个参数内都处于连续统上。我们讨论了这种连续统如何影响疫苗效力评估的方式,以及记忆群体对保护性免疫的适宜性。