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Updated: Jul 19, 2026

Humanized NOD/SCID/IL2rγnull (hu-NSG) Mouse Model for HIV Replication and Latency Studies
Published on: January 7, 2019
Normalized CD8+ but not CD4+ lymphocyte IL-2 expression is associated with early treatment with highly active
Toks Akerele1, Grazyna Galatowicz, Catey Bunce
1Institute of Ophthalmology, Moorfields Eye Hospital, City Road, London, UK.
Insights
Highly active antiretroviral therapy (HAART) improves CD4+ and CD8+ lymphocyte function in HIV/AIDS patients. Interferon-gamma production increases with HAART, especially with higher CD4 counts, while Interleukin-2 production normalizes early in CD8+ cells.
Area of Science:
- Immunology
- Virology
- Cellular Biology
Background:
- HIV/AIDS significantly impairs CD4+ and CD8+ T-lymphocyte function.
- Understanding T-cell cytokine profiles is crucial for assessing antiretroviral therapy efficacy.
Purpose of the Study:
- To assess the impact of highly active antiretroviral therapy (HAART) on CD4+ and CD8+ lymphocyte cytokine production in HIV/AIDS patients.
- To investigate the relationship between cytokine expression and clinical parameters like viral load and CD4+ T-cell counts.
Main Methods:
- Single-cell flow cytometry was used to measure Interferon-gamma (IFNγ) and Interleukin-2 (IL-2) production by CD4+ and CD8+ lymphocytes.
- Sixty-eight HIV patients were categorized based on HAART status, viral load, and CD4+ T-cell counts.
Main Results:
- IFNγ production by both CD4+ and CD8+ lymphocytes was elevated in HIV patients on HAART compared to controls, particularly when CD4+ counts exceeded 200 cells/mm³.
- CD4+ IL-2 production remained low despite HAART, while CD8+ IL-2 production improved significantly with HAART and normalized when viral load was <50 copies/ml.
- Early normalization of CD8+ IL-2 production was observed even with modest increases in CD4+ T-cell counts.
Conclusions:
- HAART effectively improves CD4+ and CD8+ T-lymphocyte responsiveness in HIV/AIDS patients.
- IFNγ elevation correlates with significant CD4+ T-cell recovery, whereas CD8+ IL-2 normalization occurs earlier in HAART treatment.
Abstract:
CD4+ and CD8+ lymphocyte cytokine production in patients with HIV/AIDS and Controls, in response to stimulation with phorbol-12-myristate-13-acetate (PMA) and ionomycin was assessed using single cell flow cytometric methods. Sixty-eight patients with HIV were divided into those on no antiretroviral therapy and those on highly active antiretroviral therapy (HAART). Patients on HAART were analyzed further on the basis of gender, ethnicity, viral load (> or =50 copies/ml), CD4 count change from nadir (>100 or <100 cells/mm(3)) and CD4 count (>200 or <200 cells/mm(3)). Interferon gamma (IFNgamma) expression by CD4+ and CD8+ lymphocytes was elevated in HIV-infected groups as compared to Controls. This elevation was statistically significant for patients on HAART but not for those not on HAART. The most significant difference was seen when the CD4+ count reached >200 cells/mm(3) (p=0.018 for CD4+ IFNgamma production and p=0.004 for CD8+ IFNgamma production). CD4+ interleukin-2 (IL-2) expression was significantly lower in HIV patients as compared to Controls but did not significantly improve however good the response to HAART. IL-2 expression by CD8+ lymphocytes was also lower in HIV patients as compared to Controls. IL-2 expression by CD8+ lymphocytes significantly improved in all patients on HAART as compared to HIV patients on no HAART. IL-2 expression was not significantly different from that of the Controls when the HIV viral load was less than 50 copies/ml. These results demonstrate improvements in both CD4+ and CD8+ responsiveness with HAART. IFNgamma production was elevated in response to HAART and was maximal only with significant CD4 count recovery. In contrast, normalization of IL-2 production by CD8+ lymphocytes was seen early in patients receiving HAART even when there was only a small increase in CD4+ lymphocyte numbers.
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