High Levels of CD57+CD28-T-Cells, Low T-Cell Proliferation and Preferential Expansion of Terminally Differentiated CD4+T-Cells in HIV-Elite Controllers

被引:14
作者
Ruiz-Mateos, Ezequiel [1 ]
Ferrando-Martinez, Sara [1 ]
Machmach, Kawthar [1 ]
Viciana, Pompeyo [1 ]
Pacheco, Yolanda M. [1 ]
Nogales, Nieves [2 ]
Genebat, Miguel [1 ]
Leal, Manuel [1 ]
机构
[1] Virgen del Rocio Univ Hosp, Infect Dis Serv, Immunovirol Lab, Biomed Inst Seville IBIS, Seville 41013, Spain
[2] Hosp Comarcal Don Benito Villanueva, Badajoz, Spain
关键词
HIV; elite-controllers; immunosenescence; activation; CD57+; proliferation; T(EM)RA; IMMUNODEFICIENCY-VIRUS TYPE-1; IMMUNE ACTIVATION; VIRAL LOAD; LYMPHOCYTE ACTIVATION; PERFORIN EXPRESSION; SEX-DIFFERENCES; RNA LEVELS; EX-VIVO; INFECTION; PROGRESSION;
D O I
10.2174/157016210793499268
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The study of clinical and demographic characteristics related to virus control and disease progression in patients who spontaneously control HIV vireamia (HIV-controllers) is of major interest. A particular cause of HIV control has not been found and the scenario could be partially explained by special homeostatic and immunological features. In this study, CD57+CD28-phenotype, T-cell activation and levels of proliferating T-cells in elite-controllers were studied in relation to spontaneous virus control. In HIV-controllers, 9% were AIDS-diagnosed and there was a high proportion of women. In elite-controllers, high T-cell CD57+ CD28-phenotype and activation levels were found and, interestingly, there was a low proliferation of total and naive T-cells and a high proliferation of the CD4+ T(EM)RA subset. Low T-cell proliferation and preferential expansion of terminally differentiated effector T-cell subsets could be an important factor for virus control in elite-controllers.
引用
收藏
页码:471 / 481
页数:11
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