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Protective Role of γδ T Cells in Different Pathogen Infections and Its Potential Clinical Application

Authors :
Yueshui Zhao
Ling Lin
Zhangang Xiao
Mingxing Li
Xu Wu
Wanping Li
Xiaobing Li
Qijie Zhao
Yuanlin Wu
Hanyu Zhang
Jianhua Yin
Lingling Zhang
Chi Hin Cho
Jing Shen
Source :
Journal of Immunology Research, Vol 2018 (2018)
Publication Year :
2018
Publisher :
Hindawi Limited, 2018.

Abstract

γδ T cells, a subgroup of T cells based on the γδ TCR, when compared with conventional T cells (αβ T cells), make up a very small proportion of T cells. However, its various subgroups are widely distributed in different parts of the human body and are attractive effectors for infectious disease immunity. γδ T cells are activated and expanded by nonpeptidic antigens (P-Ags), major histocompatibility complex (MHC) molecules, and lipids which are associated with different kinds of pathogen infections. Activation and proliferation of γδ T cells play a significant role in diverse infectious diseases induced by viruses, bacteria, and parasites and exert their potential effector function to effectively eliminate infection. It is well known that many types of infectious diseases are detrimental to human life and health and give rise to high incidence of illnesses and death rate all over the world. To date, there is no comprehensive understanding of the correlation between γδ T cells and infectious diseases. In this review, we will focus on the various subgroups of γδ T cells (mainly Vδ1 T cells and Vδ2 T cells) which can induce multiple immune responses or effective functions to fight against common pathogen infections, such as Mycobacterium tuberculosis, Listeria monocytogenes, influenza viruses, HIV, EBV, and HBV. Hopefully, the gamma-delta T cell study will provide a novel effective way to treat infectious diseases.

Details

Language :
English
ISSN :
23148861 and 23147156
Volume :
2018
Database :
Directory of Open Access Journals
Journal :
Journal of Immunology Research
Publication Type :
Academic Journal
Accession number :
edsdoj.886bc088017749d391ec12abe7663f14
Document Type :
article
Full Text :
https://doi.org/10.1155/2018/5081634