HCV coinfection contributes to HIV pathogenesis by increasing immune exhaustion in CD8 T-cells

被引:20
|
作者
Rallon, Norma [1 ,2 ]
Garcia, Marcial [1 ,2 ]
Garcia-Samaniego, Javier [3 ]
Rodriguez, Noelia [1 ,2 ]
Cabello, Alfonso [4 ]
Restrepo, Clara [1 ,2 ]
Alvarez, Beatriz [4 ]
Garcia, Rosa [4 ]
Gorgolas, Miguel [4 ]
Benito, Jose M. [1 ,2 ]
机构
[1] UAM, IIS Fdn Jimenez Diaz, Madrid, Spain
[2] Hosp Univ Rey Juan Carlos, Mostoles, Spain
[3] Hosp Univ Carlos III La Paz, Madrid, Spain
[4] Univ Hosp Fdn Jimenez Diaz, Madrid, Spain
来源
PLOS ONE | 2017年 / 12卷 / 03期
关键词
HEPATITIS-C VIRUS; ACTIVE ANTIRETROVIRAL THERAPY; DISEASE PROGRESSION; HIV-1-INFECTED PATIENTS; ELEVATED FREQUENCIES; HCV/HIV COINFECTION; PROGRAMMED DEATH-1; NATURAL-HISTORY; INFECTION; EXPRESSION;
D O I
10.1371/journal.pone.0173943
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background There are several contributors to HIV-pathogenesis or insufficient control of the infection. However, whether HIV/HCV-coinfected population exhibits worst evolution of HIV-pathogenesis remains unclear. Recently, some markers of immune exhaustion have been proposed as preferentially upregulated on T-cells during HIV-infection. Herein, we have analyzed T-cell exhaustion together with several other contributors to HIV-pathogenesis that could be affected by HCV-coinfection. Patients and methods Ninety-six patients with chronic HIV-infection (60 HIV-monoinfected and 36 HIV/HCV-coinfected), and 20 healthy controls were included in the study. All patients were untreated for both infections. Several CD4 and CD8 T-cell subsets involved in HIV-pathogenesis were investigated. Non-parametric tests were used to establish differences between groups and associations between variables. Multivariate linear regression was used to ascertain the variables independently associated with CD4 counts. Results HIV-patients presented significant differences compared to healthy controls in most of the parameters analyzed. Both HIV and HIV/HCV groups were comparable in terms of age, CD4 counts and HIV-viremia. Compared to HIV group, HIV/HCV group presented significantly higher levels of exhaustion (Tim3(+)PD1(-) subset) in total CD8(+) T-cells (p = 0.003), and higher levels of exhaustion in CD8(+) HLADR(+) CD38(+) (p = 0.04), CD8(+) HLADR(-)CD38(+) (p = 0.009) and CD8(+) HLADR(-)CD38(-) (P = 0.006) subsets of CD8(+) T-cells. Interestingly these differences were maintained after adjusting by CD4 counts and HIV-viremia. Conclusions We show a significant impact of HCV-coinfection on CD8 T-cells exhaustion, an important parameter associated with CD8 T-cell dysfunction in the setting of chronic HIV-infection. The relevance of this phenomenon on immunological and/or clinical HIV progression prompts HCV treatment to improve management of coinfected patients.
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页数:11
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