Mother-to-Child HIV Transmission With In Utero Dolutegravir vs. Efavirenz in Botswana.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
01 07 2020
Historique:
pubmed: 21 3 2020
medline: 5 1 2021
entrez: 21 3 2020
Statut: ppublish

Résumé

A large-scale evaluation of mother-to-child transmission (MTCT) with dolutegravir (DTG)-based antiretroviral treatment (ART) has not been conducted previously. Botswana was the first African country to change from efavirenz (EFV)/tenofovir (TDF)/emtricitabine (FTC) to DTG/TDF/FTC first-line ART. From April 2015 to July 2018, the Early Infant Treatment Study offered HIV DNA testing at <96 hours of life. Maternal ART regimen was available for screened infants who could be linked to the separate Tsepamo surveillance study database. We evaluated characteristics of HIV-positive infants, and compared MTCT rates by ART regimen for linked infants. Of 10,622 HIV-exposed infants screened, 42 (0.40%) were HIV-positive. In total, 5064 screened infants could be linked to the surveillance database, including 1235 (24.4%) exposed to DTG/TDF/FTC and 2411 (47.6%) exposed to EFV/TDF/FTC. MTCT was rare when either regimen was started before conception: 0/213 [0.00%, 95% confidence interval (CI): 0.00% to 1.72%] on DTG, 1/1497 (0.07%, 95% CI: 0.00% to 0.37%) on EFV. MTCT was similar for women starting each ART regimen in pregnancy: 8/999 (0.80%, 95% CI: 0.35% to 1.57%) for DTG and 8/883 (0.91%, 95% CI: 0.39% to 1.78%) for EFV (risk difference 0.11%, 95% CI: -0.79% to 1.06%). Most MTCT events (4/8 with DTG, 6/9 with EFV) occurred when ART was started <90 days before delivery. Infants exposed to DTG in utero had lower baseline HIV RNA compared with other HIV-infected infants. In utero MTCT in Botswana remains rare in the DTG era. No significant MTCT differences were observed between DTG/TDF/FTC and EFV/TDF/FTC. Risk was highest for both groups when ART was started in the third trimester.

Sections du résumé

BACKGROUND
A large-scale evaluation of mother-to-child transmission (MTCT) with dolutegravir (DTG)-based antiretroviral treatment (ART) has not been conducted previously.
SETTING
Botswana was the first African country to change from efavirenz (EFV)/tenofovir (TDF)/emtricitabine (FTC) to DTG/TDF/FTC first-line ART.
METHODS
From April 2015 to July 2018, the Early Infant Treatment Study offered HIV DNA testing at <96 hours of life. Maternal ART regimen was available for screened infants who could be linked to the separate Tsepamo surveillance study database. We evaluated characteristics of HIV-positive infants, and compared MTCT rates by ART regimen for linked infants.
RESULTS
Of 10,622 HIV-exposed infants screened, 42 (0.40%) were HIV-positive. In total, 5064 screened infants could be linked to the surveillance database, including 1235 (24.4%) exposed to DTG/TDF/FTC and 2411 (47.6%) exposed to EFV/TDF/FTC. MTCT was rare when either regimen was started before conception: 0/213 [0.00%, 95% confidence interval (CI): 0.00% to 1.72%] on DTG, 1/1497 (0.07%, 95% CI: 0.00% to 0.37%) on EFV. MTCT was similar for women starting each ART regimen in pregnancy: 8/999 (0.80%, 95% CI: 0.35% to 1.57%) for DTG and 8/883 (0.91%, 95% CI: 0.39% to 1.78%) for EFV (risk difference 0.11%, 95% CI: -0.79% to 1.06%). Most MTCT events (4/8 with DTG, 6/9 with EFV) occurred when ART was started <90 days before delivery. Infants exposed to DTG in utero had lower baseline HIV RNA compared with other HIV-infected infants.
CONCLUSION
In utero MTCT in Botswana remains rare in the DTG era. No significant MTCT differences were observed between DTG/TDF/FTC and EFV/TDF/FTC. Risk was highest for both groups when ART was started in the third trimester.

Identifiants

pubmed: 32195745
doi: 10.1097/QAI.0000000000002338
pmc: PMC7293566
mid: NIHMS1575421
pii: 00126334-202007010-00001
doi:

Substances chimiques

Alkynes 0
Anti-HIV Agents 0
Anti-Retroviral Agents 0
Benzoxazines 0
Cyclopropanes 0
Cytochrome P-450 CYP2B6 Inducers 0
Cytochrome P-450 CYP2C19 Inhibitors 0
Cytochrome P-450 CYP2C9 Inhibitors 0
Cytochrome P-450 CYP3A Inducers 0
Drug Combinations 0
Heterocyclic Compounds, 3-Ring 0
Oxazines 0
Piperazines 0
Pyridones 0
Reverse Transcriptase Inhibitors 0
Tenofovir 99YXE507IL
dolutegravir DKO1W9H7M1
Emtricitabine G70B4ETF4S
efavirenz JE6H2O27P8

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

235-241

Subventions

Organisme : NIAID NIH HHS
ID : U01 AI114235
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD080471
Pays : United States
Organisme : NIAID NIH HHS
ID : K24 AI131924
Pays : United States
Organisme : NICHD NIH HHS
ID : R01 HD095766
Pays : United States
Organisme : NICHD NIH HHS
ID : K23 HD088230
Pays : United States

Références

J Virus Erad. 2018 Apr 01;4(2):66-71
pubmed: 29682297
Am J Obstet Gynecol. 2014 Sep;211(3):297.e1-6
pubmed: 24746998
J Acquir Immune Defic Syndr. 2010 May 1;54(1):35-41
pubmed: 20216425
J Int AIDS Soc. 2018 May;21(5):e25111
pubmed: 29852062
N Engl J Med. 2019 Aug 29;381(9):827-840
pubmed: 31329379
J Int AIDS Soc. 2019 Jun;22(6):e25290
pubmed: 31180186
Lancet HIV. 2016 Nov;3(11):e510-e520
pubmed: 27658869
Sci Rep. 2016 Oct 10;6:34526
pubmed: 27721453
Pediatr Infect Dis J. 2019 May;38(5):508-512
pubmed: 30985546
AIDS. 2008 Jan 11;22(2):289-99
pubmed: 18097232
J Med Virol. 2016 Nov;88(11):1936-43
pubmed: 27037910
J Infect Dis. 2015 Jan 15;211(2):197-205
pubmed: 25081933
Sex Transm Infect. 2012 Dec;88 Suppl 2:i44-51
pubmed: 23172345
AIDS. 1999 Feb 25;13(3):407-14
pubmed: 10199232
PLoS One. 2015 Jul 01;10(7):e0132262
pubmed: 26132142
J Antimicrob Chemother. 2016 Feb;71(2):480-3
pubmed: 26538508
Antivir Ther. 2013;18(4):585-90
pubmed: 23183881
PLoS One. 2015 May 19;10(5):e0126647
pubmed: 25992639
Lancet HIV. 2018 Aug;5(8):e457-e467
pubmed: 29958853
J Med Virol. 1998 Feb;54(2):113-7
pubmed: 9496369
AIDS. 2001 Mar 9;15(4):517-22
pubmed: 11242149
HIV Med. 2017 Feb;18(2):80-88
pubmed: 27353189
Pediatrics. 2019 Jun;143(6):
pubmed: 31101703
J Clin Microbiol. 2012 Feb;50(2):502-5
pubmed: 22162550
AIDS. 2015 Nov 28;29(18):2534-7
pubmed: 26372490
Lancet HIV. 2019 Feb;6(2):e116-e127
pubmed: 30503325
Ann Intern Med. 2019 May 7;170(9):614-625
pubmed: 30934067
J Acquir Immune Defic Syndr. 2018 Feb 1;77(2):212-216
pubmed: 29084045
Eur J Clin Microbiol Infect Dis. 2018 Mar;37(3):495-500
pubmed: 29396773

Auteurs

Sonya Davey (S)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Perelman School of Medicine at University of Pennsylvania, Philadelphia, PA.

Gbolahan Ajibola (G)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Kenneth Maswabi (K)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Maureen Sakoi (M)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Kara Bennett (K)

Bennett Statistical Consulting, Inc., Ballston Lake, NY.

Michael D Hughes (MD)

Departments of Biostatistics; and.

Arielle Isaacson (A)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Modiegi Diseko (M)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Rebecca Zash (R)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA.
Division of Infectious Diseases, Beth Israel Deaconess Medical Center, Boston, MA.

Oganne Batlang (O)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Sikhulile Moyo (S)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA.

Shahin Lockman (S)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA.
Division of Infectious Diseases, Brigham and Women's Hospital, Boston, MA; and.

Mathias Lichterfeld (M)

Division of Infectious Diseases, Brigham and Women's Hospital, Boston, MA; and.
Harvard Medical School, Boston, MA.

Daniel R Kuritzkes (DR)

Division of Infectious Diseases, Brigham and Women's Hospital, Boston, MA; and.
Harvard Medical School, Boston, MA.

Joseph Makhema (J)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.

Roger Shapiro (R)

Botswana Harvard AIDS Institute Partnership, Gaborone, Botswana.
Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, MA.
Division of Infectious Diseases, Beth Israel Deaconess Medical Center, Boston, MA.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH