Cytotoxic CD4+ T-cells during HIV infection: Targets or weapons?

被引:16
|
作者
Sanchez-Martinez, Alexandra [1 ]
Perdomo-Celis, Federico [1 ]
Acevedo-Saenz, Liliana [1 ,2 ]
Rugeles, Maria T. [1 ]
Velilla, Paula A. [1 ]
机构
[1] Univ Antioquia, Fac Med, Grp Inmunovirol, Medellin, Colombia
[2] Univ CES, Fac Enfermeria, Grp Invest Enfermeria CES, Medellin, Colombia
关键词
CD4; Cytotoxic; CD107a; Granzyme B; Perforin; HIV; COMBINATION ANTIRETROVIRAL THERAPY; EFFECTOR FUNCTIONS; ANTIGEN; REPLICATION; RESPONSES; CD4+; EXPRESSION; IDENTIFICATION; INDUCTION; RECONSTITUTION;
D O I
10.1016/j.jcv.2019.08.004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Classically, CD4(+) T-cells have been referred as cytokine-producing cells and important players in immune responses by providing soluble factors that potentiate several effector immune functions. However, it is now evident that CD4(+) T-cells can also elaborate cytotoxic responses, inducing apoptosis of target cells. Cytotoxic CD4(+) T cells (CD4(+) CTLs), exhibit cytolytic functions that resemble those of CD8(+) T-cells; in fact, there is evidence suggesting that they may have a role in the control of viral infections. In this article, we discuss the role of CD4(+) CTLs during HIV infection, where CD4(+) CTLs have been associated with viral control and slow disease progression. In addition, we address the implication of CD4(+) CTLs in the context of antiretroviral therapy and the partial reconstitution of CD8(+) T-cells effector function.
引用
收藏
页码:17 / 23
页数:7
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