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Randomized Controlled Trial
. 2022 May 1;90(1):56-61.
doi: 10.1097/QAI.0000000000002917.

Brief Report: Blood and Genital Fluid Viral Load Trajectories Among Treated and Untreated Persons With Acute HIV Infection in Malawi

Affiliations
Randomized Controlled Trial

Brief Report: Blood and Genital Fluid Viral Load Trajectories Among Treated and Untreated Persons With Acute HIV Infection in Malawi

Jane S Chen et al. J Acquir Immune Defic Syndr. .

Abstract

Background: Persons with acute HIV infection (AHI) are highly infectious and responsible for a disproportionate share of incident infections. Immediate antiretroviral therapy (ART) rapidly reduces blood viral loads (VLs), but genital VLs after ART initiation during AHI are less well described.

Setting: Lilongwe, Malawi, 2012-2014.

Methods: HIV-seronegative and HIV-serodiscordant persons aged ≥18 years were screened for AHI (RNA positive) and randomized to standard of care, behavioral intervention, or behavioral intervention plus short-term ART (raltegravir/emtricitabine/tenofovir) (1:2:2). Persons who were ART eligible under Malawi guidelines could receive first-line therapy. Blood and genital VLs were assessed at weeks 1, 4, 8, and 12. Fisher's Exact test was used to compare viral suppression by ART status.

Results: Overall, 46 persons with AHI were enrolled; of whom, 17 started ART within 12 weeks. Median blood VL at AHI diagnosis was 836,115 copies/mL. At week 12, 7% (1/14) of those who initiated ART had a blood VL of ≥400 copies/mL, compared with 100% (23/23; P < 0.0001) of those who did not initiate ART (median VL: 61,605 copies/mL). Median genital VL at week 1 was 772 copies/mL, with 13 of 22 (59%) having VL of ≥400 copies/mL. At week 12, 0 of 10 (0%) of those who initiated ART had genital VL of ≥400 copies/mL, compared with 7 of 15 (47%) of those who did not initiate ART (P = 0.02).

Conclusion: Although highly correlated, VLs in blood and genital fluids occupy discrete biological compartments with distinct virologic dynamics. Our results corroborate the dramatic reduction in both compartments after ART initiation. Increasing AHI screening and rapidly initiating treatment is key to interrupting transmission.

Trial registration: ClinicalTrials.gov NCT01450189.

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Conflict of interest statement

Supported by National Institutes of Health, National Institute of Allergy and Infectious Diseases [R01 AI083059 to W.C.M.; T32AI007001 to S.E.R.]; and the University of North Carolina Center for AIDS Research (CFAR) [P30 AI050410]. Merck & Co provided raltegravir. Gilead provided emtricitabine/tenofovir. M.S.C. is on the Advisory Board for Merck and Gilead. The remaining authors have no conflicts of interest to disclose.

Figures

Figure 1.
Figure 1.
Viral loads stratified by ART initiation and biological sex, by compartment Acronyms: VL: viral load; ART: antiretroviral therapy Dashed grey line denotes cut-off for undetectable viral loads (400 copies/mL or 2.6 log10 copies/mL) Blood VL Panel: Top left: females who did not initiate ART within 12 weeks; Top right: males who did not initiate ART within 12 weeks. Bottom left: females who initiated ART within 12 weeks; Bottom right: males who initiated ART within 12 weeks. Genital VL Panel: Top left: females who did not initiate ART within 12 weeks; Top right: males who did not initiate ART within 12 weeks. Bottom left: females who initiated ART within 12 weeks; Bottom right: males who initiated ART within 12 weeks.

References

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