Editor: Willem van Eden
Changes in T-cell subpopulations during four years of suppression of HIV-1 replication in patients with advanced disease
Version of Record online: 26 JAN 2006
FEMS Immunology & Medical Microbiology
Volume 46, Issue 3, pages 351–359, April 2006
How to Cite
Lepej, S. Ž., Begovac, J. and Vince, A. (2006), Changes in T-cell subpopulations during four years of suppression of HIV-1 replication in patients with advanced disease. FEMS Immunology & Medical Microbiology, 46: 351–359. doi: 10.1111/j.1574-695X.2005.00034.x
- Issue online: 21 FEB 2006
- Version of Record online: 26 JAN 2006
- Received 5 July 2005; revised 1 September 2005; accepted 20 September 2005.
- immune reconstitution;
We compared the number/percentages of naive and memory CD4+ T-cells, CD38+CD8+ T-cells, and CD28+CD4+ and CD28+CD8+ T-cells in patients with advanced HIV disease (baseline CD4+ count<100) with those with less advanced (baseline CD4+ cell count>100) HIV disease during 4 years of suppressive highly active antiretroviral therapy. This prospective, longitudinal study included 30 treatment-naive patients and 32 controls. Advanced HIV-infected patients (n=13) gained more CD4+ T-cells than less advanced patients (n=11) at 1 month (median: 60 vs. 36μL−1), 3 months (86 vs. 14), 6 months (111 vs. 23), 12 months (174 vs. 47), 24 months (162 vs. 72) and 48 months (257 vs. 123) (P=0.15, P<0.001, P=0.026, P=0.021, P=0.1 and P=0.06, respectively). Advanced patients gained more naive CD4+ T-cells at 48 months compared to less advanced patients (27.3 vs. 11.4%, P=0.05). The relative gain in memory CD4+ T-cells was greater in advanced vs. less advanced patients at 1 month (median: 6.4 vs. 1.4%), 3 months (4.3 vs. 2.0), 6 months (6.7 vs. 1.6), 12 months (6.9 vs. 2.4), 24 months (7.5 vs. 3.1) and 48 months (11.3 vs. 6.8) (P=0.002, P=0.013, P<0.001, P=0.004, P=0.001 and P=0.015, respectively). At 48 months, CD38+CD8+ T-cells and naive CD4+ T-cells reached normal values (9.2%, P=0.869 vs. controls and 47.5%, P=0.699, respectively) in less advanced patients, as did CD38+CD8+ T-cells in advanced patients (4.7%, P=0.309 vs. controls). The kinetics of naive and memory CD4+ T-cell reconstitution is different in less advanced compared to advanced HIV patients.