Articles > CD8 apoptosis may be a predictor of T cell number normalization after immune reconstitution in HIV

CD8 apoptosis may be a predictor of T cell number normalization after immune reconstitution in HIV

CD8 apoptosis may be a predictor of T cell number normalization after immune reconstitution in HIV

Dorothy E Lewis,6, Kimber L Gross2, Martine M Diez,5 ,6, Maria L Martinez,6, Helen N Lukefahr,6, Claudia A Kozinetz,6 and Roberto C Arduino,6

1Department of Immunology, Baylor College of Medicine, Houston, Texas, USA
2Department of Mathematics, University of Houston, Houston, Texas, USA
3Department of Medicine, University of Texas-Houston Health Sciences, Houston, Texas, USA
4Department of Pediatrics, Baylor College of Medicine, Houston, Texas, USA
5Cambridge University, UK
6Baylor College of Medicine/University of Texas Center for AIDS Research, Houston, Texas, USA

Background

As part of the Houston Vanguard study, a subset of 10 patients randomized to receive IL-2 therapy were compared to 4 patients randomized to not receive IL-2, for markers of T cell activation and death during the first three cycles of IL-2. All patients were treated with combination antiretroviral therapy (ART) and were virally suppressed. The purpose of the study was to examine the role of CD8+ T cell death in responses to ART and IL-2 therapy.

Methods

Lymphocytes were examined at Day 0, 5 and 30 days during three cycles of IL-2 therapy. CD25, CD38, HLA-DR expression and annexin (cell death) were examined on CD4 and CD8 subpopulations. Follow up studies examined CD4 levels and CD4:CD8 reconstitution after 6 years using both univariant and multivariate analyses.

Results

Human lymphocytes responded to IL-2 therapy by upregulation of CD25 on CD4+ T cells, leading to an increase in CD4 cell counts. CD8+ T cells did not increase CD25 expression, but upregulated activation antigens (CD38 and DR) and had increased death. At baseline, 7 of the 14 patients had high CD8+ T cell apoptosis (mean 17.0% ± 6.0). We did an exploratory analysis of immune status after six years, and found that baseline CD8+ T cell apoptosis was correlated with CD4 cell count gain beginning two years post enrollment. Patients with low levels of CD8+ T cell apoptosis at baseline (mean 2.2% ± 2.1) had significantly higher CD4 cell counts and more normalized CD4:CD8 ratios than patients with high CD8+ T cell apoptosis (mean CD4 cell counts 1,209 ± 164 vs 754 ± 320 cells/mm3; CD4:CD8 ratios 1.55 vs. 0.70, respectively).

Conclusion

We postulate that CD8+ T cell apoptosis may reflect inherent activation status, which continues in some patients even though viral replication is suppressed which influences the ability of CD4+ T cells to rebound. Levels of CD8+ T cell apoptosis may therefore be an independent predictor of immune status, which should be shown in a prospective study.

Journal of Translational Medicine 2007, 5:9. This is an open access article distributed under the terms of the Creative Commons Attribution License.


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