NKG2D Expression on HIV-Specific CD8+ T cells Is Reduced in Viremic HIV-1-Infected Patients but Maintained in HIV Controllers

被引:3
作者
Lecuroux, Camille [1 ]
Saez-Cirion, Asier [2 ]
Noel, Nicolas [1 ]
Ben-Lamine, Lilia [1 ]
Girault, Isabelle [1 ]
Caillat-Zucman, Sophie [3 ]
Scott-Algara, Daniel [2 ]
Venet, Alain [1 ]
Lambotte, Olivier [1 ,4 ,5 ]
机构
[1] INSERM, U1012, F-94275 Le Kremlin Bicetre, France
[2] Inst Pasteur, Unite Regulat Infect Retrovirales, Paris, France
[3] Hop St Vincent de Paul, INSERM, U986, F-75674 Paris, France
[4] Univ Paris 11, U1012, Le Kremlin Bicetre, France
[5] Hop Bicetre, AP HP, Serv Med Interne & Malad Infect, Le Kremlin Bicetre, France
关键词
NKG2D; HIV-specific CD8(+) T lymphocytes; inflammation; HIV controllers; NATURAL-KILLER-CELLS; ACTIVATION; INFECTION; RECEPTOR; LIGANDS; IMMUNORECEPTOR; LYMPHOCYTES; ABSENCE; RNA;
D O I
10.1097/QAI.0b013e318274579f
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
NKG2D mediates an important costimulatory pathway in CD8(+) T cells. In HIV infection, the authors found that NKG2D expression on both total CD8(+) and HIV-specific CD8(+) T cells was significantly lower in viremic patients than in HIV controllers. Antiretroviral therapy partially restored NKG2D expression on HIV-specific CD8(+) T cells. The authors observed a negative correlation between the respective expression levels of CD38 and NKG2D on total CD8(+) and HIV-specific CD8(+) T cells. The maintenance of NKG2D expression on CD8(+) T cells in HIV controllers may contribute to better cell function.
引用
收藏
页码:17 / 20
页数:4
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