T Cell Development and Function

被引:11
|
作者
Adu-Berchie, Kwasi [1 ,2 ]
Obuseh, Favour O. [2 ,3 ]
J. Mooney, David [1 ,2 ,4 ]
机构
[1] Harvard Univ, John A Paulson Sch Engn & Appl Sci, Cambridge, MA USA
[2] Harvard Univ, Wyss Inst Biolog Inspired Engn, Boston, MA USA
[3] Harvard-MIT Hlth Sci & Technol, Cambridge, MA USA
[4] Harvard Univ, John A Paulson Sch Engn & Appl Sci, 29 Oxford St, Cambridge, MA 02138 USA
基金
英国惠康基金; 美国国家卫生研究院;
关键词
T cells; immunology; cancer; immunotherapy; development; function; EXTRACELLULAR-MATRIX; SUPPRESSOR-CELLS; LYMPH-NODE; DENDRITIC CELLS; CANCER; MICROENVIRONMENT; DIFFERENTIATION; EXHAUSTION; METASTASIS; SENESCENCE;
D O I
10.1089/rej.2023.0015
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
T cells play critical roles in the immune system, including in responses to cancer, autoimmunity, and tissue regeneration. T cells arise from common lymphoid progenitors (CLPs) that differentiate from hematopoietic stem cells in the bone marrow. CLPs then traffic to the thymus, where they undergo thymopoiesis through a number of selection steps, resulting in mature single positive naive CD4 helper or CD8 cytotoxic T cells. Naive T cells are home to secondary lymphoid organs like lymph nodes and are primed by antigen-presenting cells, which scavenge for both foreign and self-antigens. Effector T cell function is multifaceted, including direct target cell lysis and secretion of cytokines, which regulate the functions of other immune cells (refer to "Graphical Abstract"). This review will discuss T cell development and function, from the development of lymphoid progenitors in the bone marrow to principles that govern T cell effector function and dysfunction, specifically within the context of cancer.
引用
收藏
页码:126 / 138
页数:13
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