Natural killer cell heterogeneity: cellular dysfunction and significance in HIV-1 immuno-pathogenesis

被引:15
作者
Ansari, A. Wahid [1 ,2 ,3 ]
Ahmad, Fareed [1 ]
Meyer-Olson, Dirk [1 ]
Kamarulzaman, Adeeba [2 ,3 ]
Jacobs, Roland [1 ]
Schmidt, Reinhold E. [1 ]
机构
[1] Hannover Med Sch, Dept Clin Immunol & Rheumatol, D-30625 Hannover, Germany
[2] Univ Malaya, Ctr Excellence Res AIDS CERiA, Kuala Lumpur 50603, Malaysia
[3] Univ Malaya, Dept Med, Fac Med, Kuala Lumpur 50603, Malaysia
关键词
Innate immunity; CD56 dim and bright; Granzyme B; Antibody-dependent cellular cytotoxicity; Highly active antiretroviral therapy; HUMAN NK CELLS; CLASS-I MOLECULES; C-VIRUS-INFECTION; T-CELLS; DENDRITIC CELLS; MEDIATED CYTOTOXICITY; HLA-B; RECEPTOR REPERTOIRES; ACTIVATING RECEPTOR; NKG2D RECEPTOR;
D O I
10.1007/s00018-015-1911-5
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
Natural killer (NK) cells are innate immune effectors that provide first line of defence against viruses. Human NK cells are heterogeneous in nature, and their functions rely on a dynamic balance between germ-line-encoded activating and inhibitory receptors. HIV-1 infection results in altered NK cell receptor repertoire and impaired effector functions including the ability to lyse virus-infected cells and secretion of antiviral cytokine IFN-gamma. Over the last decade, additional NK cell subset-specific molecules have been identified, leading to emergence of a more complex cellular diversity than previously thought. Herein, we discuss NK cell subset redistribution, altered receptor repertoire and influence of interaction of polymorphic leucocyte antigen (HLA) and killer cell immunoglobulin-like receptors (KIR) on HIV-1 disease progression.
引用
收藏
页码:3037 / 3049
页数:13
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