CD8 T-cell regulation by T regulatory cells and the programmed cell death protein 1 pathway

被引:11
作者
Penaloza-MacMaster, Pablo [1 ]
机构
[1] Northwestern Univ, Feinberg Sch Med, Dept Microbiol Immunol, 303 E Chicago Ave Tarry 6-728, Chicago, IL 60611 USA
关键词
immune checkpoints; immune exhaustion; immune memory; lymphocytic choriomeningitis virus; regulatory T cells; CHRONIC VIRAL-INFECTION; FRIEND RETROVIRUS INFECTION; PD-L1; EXPRESSION; CHECKPOINT BLOCKADE; TISSUE DESTRUCTION; GENE AMPLIFICATION; ANTITUMOR IMMUNITY; VIRUS-INFECTION; CANCER-PATIENTS; BREAST-CANCER;
D O I
10.1111/imm.12739
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The primary function of the immune system is to protect the host from infectious microorganisms and cancers. However, a major component of the immune response involves the direct elimination of cells in the body and the induction of systemic inflammation, which may result in life-threatening immunopathology. Therefore, the immune system has developed complex mechanisms to regulate itself with a specialized subset of CD4 T lymphocytes (referred to as regulatory T cells) and immune checkpoint pathways, such as the programmed cell death protein 1 pathway. These immune regulatory mechanisms can be exploited by pathogens and tumours to establish persistence in the host, warranting a deeper understanding of how to fine-tune immune responses during these chronic diseases. Here, I discuss various features of immune regulatory pathways and what important aspects must be considered in the next generation of therapies to reverse immune exhaustion, understanding that this process is a natural mechanism to prevent the host from destroying itself.
引用
收藏
页码:146 / 153
页数:8
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