4.6 Article

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

Journal

PLOS ONE
Volume 12, Issue 3, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0173943

Keywords

-

Funding

  1. Plan Nacional I+0+I [RD12/0017/0031, PI14/00518]
  2. ISCIII-Subdireccion General de Evaluacion
  3. European Regional Development Fund (Fondos FEDER)
  4. ISCIII, Madrid, Spain [CP14/00198]
  5. Intramural Research Scholarship from IIS-FJD

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available