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Author Notes:

Correspondence: Rakhi Malhotra, Email: rakhi_shai@uab.edu and Liangyuan Hu, Email: lyhu@uab.edu

Authors' contributions: RM* performed the statistical analyses and participated in the preparation of multiple drafts of the manuscript.

LH* performed the laboratory work, participated in the statistical analyses and participated in the preparation of multiple drafts of the manuscript.

WS assisted in planning the laboratory work, performed the assays, and reviewed the manuscript.

IB prepared analytic data sets of the clinical, epidemiologic, and genetic data; and assisted in editing the manuscript.

JM organized the cohort studies, supervised the data collection in the field and reviewed the manuscript.

SA conceived the cohort studies, participated in the design of the genetic substudies, and reviewed the analyses and the manuscript.

EH participated in the design of the genetic substudies, supervised the performance of the viral sequencing and viral load measurements, and reviewed the manuscript.

SS participated in the analyses and in the editing of the manuscript.

JT participated in the design of the genetic substudies, supervised all aspects of the genotyping, participated in the analyses and reviewed multiple drafts of the manuscript.

RAK conceived the genetics studies, supervised the statistical analyses, and reviewed and edited all drafts of the manuscript.

Acknowledgements: We thank study participants, staff, interns, and Project Management Group members of the Zambia-Emory HIV Research Project in Lusaka, Zambia; technical staff and students at the virology laboratory at the University Teaching Hospital, Lusaka, the immunogenetics laboratory at UAB School of Public Health; and the data analysis group at UAB school of Public Health.

Disclosures: The authors declare that they have no competing interests.

Subject:

Association of chemokine receptor gene (CCR2-CCR5) haplotypes with acquisition and control of HIV-1 infection in Zambians

Tools:

Journal Title:

Retrovirology

Volume:

Volume 8, Number 22

Publisher:

, Pages 1-9

Type of Work:

Article | Final Publisher PDF

Abstract:

Background Polymorphisms in chemokine (C-C motif) receptors 2 and 5 genes (CCR2 and CCR5) have been associated with HIV-1 infection and disease progression. We investigated the impact of CCR2-CCR5 haplotypes on HIV-1 viral load (VL) and heterosexual transmission in an African cohort. Between 1995 and 2006, cohabiting Zambian couples discordant for HIV-1 (index seropositive and HIV-1 exposed seronegative {HESN}) were monitored prospectively to determine the role of host genetic factors in HIV-1 control and heterosexual transmission. Genotyping for eight CCR2 and CCR5 variants resolved nine previously recognized haplotypes. By regression and survival analytic techniques, controlling for non-genetic factors, we estimated the effects of these haplotypic variants on a) index partner VL, b) seroconverter VL, c) HIV-1 transmission by index partners, d) HIV-1 acquisition by HESN partners. Results Among 567 couples, 240 virologically linked transmission events had occurred through 2006. HHF*2 homozygosity was associated with significantly lower VL in seroconverters (mean beta = -0.58, log10 P = 0.027) and the HHD/HHE diplotype was associated with significantly higher VL in the seroconverters (mean beta = 0.54, log10 P = 0.014) adjusted for age and gender in multivariable model. HHD/HHE was associated with more rapid acquisition of infection by the HESNs (HR = 2.0, 95% CI = 1.20-3.43, P = 0.008), after adjustments for index partner VL and the presence of genital ulcer or inflammation in either partner in Cox multivariable models. The HHD/HHE effect was stronger in exposed females (HR = 2.1, 95% CI = 1.14-3.95, P = 0.018). Conclusions Among Zambian discordant couples, HIV-1 coreceptor gene haplotypes and diplotypes appear to modulate HIV-1 VL in seroconverters and alter the rate of HIV-1 acquisition by HESNs. These associations replicate or resemble findings reported in other African and European populations.

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© 2011 Malhotra et al; licensee BioMed Central Ltd.

This is an Open Access work distributed under the terms of the Creative Commons Attribution 2.0 Generic License (http://creativecommons.org/licenses/by/2.0/).

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