Depot Medroxyprogesterone Acetate and the Vaginal Microbiome as Modifiers of Tenofovir Diphosphate and Lamivudine Triphosphate Concentrations in the Female Genital Tract of Ugandan Women: Implications for Tenofovir Disoproxil Fumarate/Lamivudine in Preexposure Prophylaxis.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
10 04 2020
Historique:
received: 03 04 2019
accepted: 24 05 2019
pubmed: 28 5 2019
medline: 7 1 2021
entrez: 28 5 2019
Statut: ppublish

Résumé

Effective concentrations of antiretrovirals in the female genital tract (FGT) are critical for suppression of viral shedding or effective preexposure prophylaxis. The disposition of tenofovir diphosphate (TFV-DP) and emtricitabine triphosphate (FTC-TP) in the FGT have been previously described. Despite widespread use, however, lamivudine triphosphate (3TC-TP) exposure in the FGT is unknown. Depot medroxyprogesterone acetate (DMPA) and vaginal dysbiosis have been implicated in increased risk of human immunodeficiency virus (HIV) acquisition, but whether they alter TFV-DP or 3TC-TP exposure, and therefore compromise prevention efficacy, is unknown. Fifty premenopausal women living with HIV in Kampala, Uganda, and receiving daily tenofovir disoproxil fumarate/lamivudine were recruited. Ectocervical biopsies were obtained for quantification of TFV-DP and 3TC-TP using liquid chromatography-mass spectrometry. 16S ribosomal RNA gene sequencing was performed on DNA extracted from vaginal swabs. Wilcoxon rank-sum was used to test for differences between contraceptive groups. 3TC-TP concentrations were on average 17-fold greater than TFV-DP concentrations in cervical tissues. TFV-DP concentrations in cervical biopsies were 76% greater in DMPA users compared with women using nonhormonal contraception (n = 23 per group). Abundance of Lactobacillus in vaginal swabs was correlated with 3TC-TP concentrations in cervical tissues. We found that TFV-DP concentrations were significantly greater in DMPA users compared with women using nonhormonal contraception, suggesting that prevention efficacy is unlikely to be compromised by DMPA use. Similar to reports of FTC-TP, 3TC-TP exposure was significantly greater than TFV-DP in cervical tissue and was correlated with abundance of Lactobacillus. These data support lamivudine as an option for preexposure prophylaxis. NCT03377608.

Sections du résumé

BACKGROUND
Effective concentrations of antiretrovirals in the female genital tract (FGT) are critical for suppression of viral shedding or effective preexposure prophylaxis. The disposition of tenofovir diphosphate (TFV-DP) and emtricitabine triphosphate (FTC-TP) in the FGT have been previously described. Despite widespread use, however, lamivudine triphosphate (3TC-TP) exposure in the FGT is unknown. Depot medroxyprogesterone acetate (DMPA) and vaginal dysbiosis have been implicated in increased risk of human immunodeficiency virus (HIV) acquisition, but whether they alter TFV-DP or 3TC-TP exposure, and therefore compromise prevention efficacy, is unknown.
METHODS
Fifty premenopausal women living with HIV in Kampala, Uganda, and receiving daily tenofovir disoproxil fumarate/lamivudine were recruited. Ectocervical biopsies were obtained for quantification of TFV-DP and 3TC-TP using liquid chromatography-mass spectrometry. 16S ribosomal RNA gene sequencing was performed on DNA extracted from vaginal swabs. Wilcoxon rank-sum was used to test for differences between contraceptive groups.
RESULTS
3TC-TP concentrations were on average 17-fold greater than TFV-DP concentrations in cervical tissues. TFV-DP concentrations in cervical biopsies were 76% greater in DMPA users compared with women using nonhormonal contraception (n = 23 per group). Abundance of Lactobacillus in vaginal swabs was correlated with 3TC-TP concentrations in cervical tissues.
CONCLUSIONS
We found that TFV-DP concentrations were significantly greater in DMPA users compared with women using nonhormonal contraception, suggesting that prevention efficacy is unlikely to be compromised by DMPA use. Similar to reports of FTC-TP, 3TC-TP exposure was significantly greater than TFV-DP in cervical tissue and was correlated with abundance of Lactobacillus. These data support lamivudine as an option for preexposure prophylaxis.
CLINICAL TRIALS REGISTRATION
NCT03377608.

Identifiants

pubmed: 31131846
pii: 5498856
doi: 10.1093/cid/ciz443
pmc: PMC7146007
doi:

Substances chimiques

Anti-HIV Agents 0
Dideoxynucleotides 0
Organophosphates 0
lamivudine triphosphate 0
tenofovir diphosphate 0
Lamivudine 2T8Q726O95
Cytidine Triphosphate 65-47-4
Tenofovir 99YXE507IL
Medroxyprogesterone Acetate C2QI4IOI2G
Emtricitabine G70B4ETF4S
Adenine JAC85A2161

Banques de données

ClinicalTrials.gov
['NCT03377608']

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1717-1724

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR002494
Pays : United States
Organisme : NIAID NIH HHS
ID : R01 AI118332
Pays : United States
Organisme : NIAID NIH HHS
ID : UM1 AI069530
Pays : United States
Organisme : NIAID NIH HHS
ID : K08 AI134262
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI050410
Pays : United States

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

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Auteurs

Melanie R Nicol (MR)

Department of Experimental and Clinical Pharmacology, University of Minnesota, Minneapolis.

Prosperity Eneh (P)

Department of Experimental and Clinical Pharmacology, University of Minnesota, Minneapolis.

Rita Nakalega (R)

Makerere University-John Hopkins University Research Collaboration, Kampala, Uganda.

Thomas Kaiser (T)

Department of Surgery, University of Minnesota, Minneapolis.

Samuel Kabwigu (S)

Makerere University-John Hopkins University Research Collaboration, Kampala, Uganda.

Esther Isingel (E)

Makerere University-John Hopkins University Research Collaboration, Kampala, Uganda.

Mags Beksinska (M)

School of Clinical Sciences, University of the Witwatersrand, Durban, South Africa.

Craig Sykes (C)

Division of Pharmacotherapy and Experimental Therapeutics, University of North Carolina at Chapel Hill.

Mary Glenn Fowler (MG)

Department of Pathology, John Hopkins University, Baltimore, Maryland.

Todd T Brown (TT)

Department of Medicine, John Hopkins University, Baltimore, Maryland.

Christopher Staley (C)

Department of Surgery, University of Minnesota, Minneapolis.

Flavia Kiweewa Matovu (F)

Makerere University-John Hopkins University Research Collaboration, Kampala, Uganda.
Department of College of Health Sciences, Makerere University, Kampala, Uganda.

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