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Sifting through CD8+ T Cell Memory
DOI:10.1016/j.immuni.2016.12.005.png)
摘要
En 中文
In this issue of Immunity, Gerlach et al. (2016) describe three distinct memory CD8(+) T cell subsets based upon expression of the fractalkine receptor CX3CR1. Their findings revise the paradigm of effector and central memory T cells by revealing a subset of CD8(+) memory T cells defined by intermediate levels of expression of CX3CR1 that conducts tissue surveillance.
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期刊
IF:
26.3
论文数:
6.4K
被引数:
7.5W
机构
引用论文
Lineage relationship and protective immunity of memory CD8 T cell subsets记忆性CD8 T细胞亚群的谱系关系和保护性免疫
NATURE IMMUNOLOGY
IF27.6
The Chemokine Receptor CX3CR1 Defines Three Antigen-Experienced CD8 T Cell Subsets with Distinct Roles in Immune Surveillance and Homeostasis
IMMUNITY
IF26.3
Protective Capacity of Memory CD8+ T Cells Is Dictated by Antigen Exposure History and Nature of the Infection
IMMUNITY
IF26.3
Phenotypic and Functional Alterations in Circulating Memory CD8 T Cells with Time after Primary Infection
PLOS PATHOGENS
IF4.9
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