Interleukin-8 Expression Under Highly Effective Host Immunological Control of HIV-1 Disease Progression

Background: Interleukin-8 (IL-8) is a pro-inflammatory chemokine involved in neutrophil recruitment and immune activation and has been implicated in HIV-1–associated inflammation and disease progression. Despite effective highly active antiretroviral therapy (HAART), residual immune activation persists in many people living with HIV, and the role of IL-8 across different stages of infection and treatment remains incompletely understood, particularly in sub-Saharan Africa. Methods: This cross-sectional study enrolled 40 participants in Osogbo, South-Western Nigeria, comprising HIV-negative controls (n=10), HAART-naïve HIV-positive individuals (OFF-HAART, n=10), HAART-treated individuals (ON-HAART, n=10), and AIDS progressors (n=10). Serum IL-8 levels were quantified using enzyme-linked immunosorbent assay, while CD4+ T-cell counts were determined by flow cytometry. Viral load, hematological indices, and selected biochemical parameters were also assessed. Associations between IL-8, immunological markers, and socio-demographic variables were analyzed using correlation and comparative statistics. Results: Interleukin-8 (IL-8) levels showed a downward trend from HIV-negative subjects (175.89 ± 84.58 pg/mL) and OFF-HAART individuals (211.14 ± 64.55 pg/mL) to ON-HAART participants (125.08 ± 39.73 pg/mL), with the lowest levels observed in AIDS progressors (11.40 ± 1.14 pg/mL), although this trend did not reach statistical significance (p = 0.088). CD4⁺ T-cell counts differed significantly across groups (p < 0.001), with marked depletion in OFF-HAART subjects (166.10 ± 41.40 cells/µL) and partial immune reconstitution in ON-HAART individuals (395.20 ± 61.69 cells/µL). Among AIDS progressors, longer infection duration was significantly associated with higher IL-8 expression (χ² = 6.667, p = 0.010). Conclusion: Elevated IL-8 is linked to impaired immune status and disease progression in HIV-1 infection, while reduced IL-8 accompanies immune recovery and advanced disease stages. IL-8 may serve as a useful biomarker of immune dysregulation and progression across HIV disease states, supporting its potential role in monitoring inflammation alongside conventional immunological markers.

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Publication Details

Journal
Iconic Research and Engineering Journals
Published
2026-04-11
DOI
https://doi.org/10.64388/irev9i10-1716192
Primary Topic
HIV Research and Treatment
Type
article
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article

Interleukin-8 Expression Under Highly Effective Host Immunological Control of HIV-1 Disease Progression

Adesola Oyekunle Oyekale, Omolade Abiodun Felix; Adegoke Adekemi Omolola, Ahmed Ibrahim Oluwaseun; Ridwan Olanrewaju Ogunola, Ibraheem Olawale Ogunola; Lawal Lukmon Abiodun et al.
Iconic Research and Engineering Journals
HIV Research and Treatment
article

Interleukin-8 Expression Under Highly Effective Host Immunological Control of HIV-1 Disease Progression

Adesola Oyekunle Oyekale, Omolade Abiodun Felix; Adegoke Adekemi Omolola, Ahmed Ibrahim Oluwaseun; Ridwan Olanrewaju Ogunola, Ibraheem Olawale Ogunola; Lawal Lukmon Abiodun, Tirimisiyu Alani Ogunola
article en

Abstract

Background: Interleukin-8 (IL-8) is a pro-inflammatory chemokine involved in neutrophil recruitment and immune activation and has been implicated in HIV-1–associated inflammation and disease progression. Despite effective highly active antiretroviral therapy (HAART), residual immune activation persists in many people living with HIV, and the role of IL-8 across different stages of infection and treatment remains incompletely understood, particularly in sub-Saharan Africa. Methods: This cross-sectional study enrolled 40 participants in Osogbo, South-Western Nigeria, comprising HIV-negative controls (n=10), HAART-naïve HIV-positive individuals (OFF-HAART, n=10), HAART-treated individuals (ON-HAART, n=10), and AIDS progressors (n=10). Serum IL-8 levels were quantified using enzyme-linked immunosorbent assay, while CD4+ T-cell counts were determined by flow cytometry. Viral load, hematological indices, and selected biochemical parameters were also assessed. Associations between IL-8, immunological markers, and socio-demographic variables were analyzed using correlation and comparative statistics. Results: Interleukin-8 (IL-8) levels showed a downward trend from HIV-negative subjects (175.89 ± 84.58 pg/mL) and OFF-HAART individuals (211.14 ± 64.55 pg/mL) to ON-HAART participants (125.08 ± 39.73 pg/mL), with the lowest levels observed in AIDS progressors (11.40 ± 1.14 pg/mL), although this trend did not reach statistical significance (p = 0.088). CD4⁺ T-cell counts differed significantly across groups (p < 0.001), with marked depletion in OFF-HAART subjects (166.10 ± 41.40 cells/µL) and partial immune reconstitution in ON-HAART individuals (395.20 ± 61.69 cells/µL). Among AIDS progressors, longer infection duration was significantly associated with higher IL-8 expression (χ² = 6.667, p = 0.010). Conclusion: Elevated IL-8 is linked to impaired immune status and disease progression in HIV-1 infection, while reduced IL-8 accompanies immune recovery and advanced disease stages. IL-8 may serve as a useful biomarker of immune dysregulation and progression across HIV disease states, supporting its potential role in monitoring inflammation alongside conventional immunological markers.

Iconic Research and Engineering JournalsVol. 9(10)
Good health and well-being
Openalex Percentile: Top 7%
HIV Research and Treatment
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