Impact of epitope density on CD8+ T cell development and function

被引:10
作者
Cosma, Gabriela L. [1 ]
Eisenlohr, Laurence C. [2 ,3 ]
机构
[1] Thomas Jefferson Univ, Dept Microbiol & Immunol, Philadelphia, PA 19107 USA
[2] Univ Penn, Perelman Sch Med, Philadelphia, PA 19104 USA
[3] Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Res Inst, Philadelphia, PA 19104 USA
关键词
CD8+T cell; MHC class I; Antigen processing and presentation; Epitope density; Immunological synapse; HIGH-AVIDITY CTL; DENDRITIC CELLS; IN-VIVO; IMMUNOLOGICAL SYNAPSE; TCR MICROCLUSTERS; ANTIGEN; IMMUNODOMINANCE; RESPONSES; ACTIVATION; MEMORY;
D O I
10.1016/j.molimm.2019.03.010
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Effective immune responses against intracellular pathogens and tumors frequently rely upon CD8+ cytotoxic T lymphocytes (CTLs). In turn, cn. detection of foreign material from viruses and bacteria depends on antigen presentation by the MHC class I pathway. The underpinnings of antigen processing and presentation and, subsequent T cell activation and immunological memory development, have been extensively studied, leading to a better understanding of the balance between antigen dose, context, and, the T cell activation threshold. Still, the complexity of this process leads to apparent contradictions that hinder construction of rational strategies for generating optimal CD8 + T cell responses in a variety of settings. In this review we consolidate the current knowledge around the effects of peptide MHC I complex (pMHC) density and kinetics on CD8 + T cell responses and function during the acute phase of an infection.
引用
收藏
页码:120 / 125
页数:6
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