4.5 Article

Activation of NK cells is associated with HIV-1 disease progression

Journal

JOURNAL OF LEUKOCYTE BIOLOGY
Volume 96, Issue 1, Pages 7-16

Publisher

OXFORD UNIV PRESS
DOI: 10.1189/jlb.0913514

Keywords

immune activation; CD38; HLA-DR; AIDS; elite controllers; controllers

Funding

  1. Mexican Government (Comision de Equidad y Genero de la H. Camara de Diputados)
  2. Instituto de Ciencia y Tecnologia del Distrito Federal (ICyTDF) [PIRIVE09-18]
  3. Fundacion Mexico Vivo
  4. National Council of Science and Technology (CONACyT) [22156]
  5. UNAM

Ask authors/readers for more resources

The main predictor of HIV-1 disease progression is CD8(+) T cell activation, characterized by elevated expression of CD38 and HLA-DR. NK cells are also activated in viremic HIV-1-infected individuals. However, the relationship between NK cell activation and HIV-1 disease progression remains undefined. We characterized NK cell activation and its association with disease progression in treatment of naive HIV-1-infected individuals, who naturally maintained low/undetectable viremia (elite and viremic controllers), compared with progressors and AIDS subjects, and treated individuals. Our results show that CD38 expression on NK cells, predominantly in the cytotoxic CD56(dim)CD16(+) subset, is associated with HIV-1 disease progression (CD4(+) T cell count and pVL), T cell activation (percentage of CD38(+)HLA-DR+ T cells), sCD14, inflammation, and innate immune activation. Moreover, NK cell activation is increased in HIV-1-infected subjects progressing to AIDS but not in elite and viremic controllers. ART partially reduces the proportion of activated NK cells. Furthermore, our results show that individuals, who naturally control viremia, maintain low levels of innate immune activation similar to those of uninfected controls.

Authors

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

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available