Host Genetics Influences HIV Reservoir Persistence, Treatment Outcomes And CCR5 Expression In Patients On Long-Term Antiretroviral Therapy In Ghana
| dc.contributor.author | Hanson, M.E. | |
| dc.contributor.author | Effah, A. | |
| dc.contributor.author | Appiah, P.K. | |
| dc.contributor.author | et al. | |
| dc.date.accessioned | 2026-10-12T15:39:03Z | |
| dc.date.issued | 2026-07-22 | |
| dc.description | Research Article | |
| dc.description.abstract | Objective: This study investigated influence of cysteine-cysteine chemokines (CCR5, CCR5-59029A/G, CCR2), and stoma cell derived factor 1 (SDF1); as AIDS restriction genes (ARGs), on treatment outcomes among people with HIV (PWH) on long term antiretroviral therapy (ART) in Ghana.Methods: This cross-sectional study was conducted among 167 PWH and receiving ART in Accra, Ghana. Genomic DNA from PBMCs was used to genotype CCR5-Δ32, CCR2-V64I, CCR5 A59029G, and SDF1-3′A variants using polymerase chain reaction-restriction fragment length polymorphism, CCR5 expression was estimated by RT-qPCR.Results: All participants carried the wild-type CCR5 genotype. No AIDS Restriction Genes was associated with virologic or immunological outcomes (p>0.05). However, individuals with the CCR5 A59029G GG genotype exhibited significantly higher proviral DNA levels than those with the AA genotype (p < 0.05), and the GG genotype independently predicted higher proviral DNA burden in multivariable analysis (β = 0.840, p = 0.011).Conclusion: No ARG variant was significantly associated with virologic or immunological outcomes. However, CCR5 A59029G was associated with differences in proviral DNA burden and CCR5 mRNA expression, suggesting a potential role in HIV reservoir dynamics during suppressive ART. | |
| dc.description.sponsorship | The author(s) declared that financial support was received for this work and/or its publication. Research reported in this publication was supported by EDCTP2 programme by the European Union (Grant No. TMA2017SF-1955, H-CRIS) awarded to GBK and the National Institute of Allergy and Infectious Diseases of the National Institutes of Health under Award Number R21AI174880 awarded to EYB. The content is solely the responsibility of the authors and does not represent the views of the Funders. | |
| dc.identifier.citation | Appiah, P. K., Bonney, E. Y., Obirikorang, C., Aboagye, J. O., Hanson, M. E., Agomuo, S. K. S., ... & Kyei, G. B. (2026). Host genetics influences HIV reservoir persistence, treatment outcomes and CCR5 expression in patients on long-term antiretroviral therapy in Ghana. Frontiers in immunology, 17, 1885690. | |
| dc.identifier.uri | https://doi.org/10.3389/fimmu.2026.1885690 | |
| dc.identifier.uri | https://ugspace.ug.edu.gh/handle/123456789/45720 | |
| dc.language.iso | en | |
| dc.publisher | Frontiers in Immunology | |
| dc.subject | HIV | |
| dc.subject | Genetics | |
| dc.subject | CCR5 | |
| dc.subject | Antiretroviral therapy | |
| dc.subject | Ghana | |
| dc.title | Host Genetics Influences HIV Reservoir Persistence, Treatment Outcomes And CCR5 Expression In Patients On Long-Term Antiretroviral Therapy In Ghana | |
| dc.type | Article |
