Role of HIV and Antiretroviral Therapy on the Expression of Placental Transporters in Women with HIV.


Journal

The AAPS journal
ISSN: 1550-7416
Titre abrégé: AAPS J
Pays: United States
ID NLM: 101223209

Informations de publication

Date de publication:
25 10 2020
Historique:
received: 12 07 2020
accepted: 28 09 2020
entrez: 25 10 2020
pubmed: 26 10 2020
medline: 9 9 2021
Statut: epublish

Résumé

Treatment guidelines recommend continuation of combination antiretroviral therapy (cART) throughout pregnancy for all women living with human immunodeficiency virus (HIV). Many of these drugs are substrates of transporters expressed in the placenta and therefore play a role in fetal exposure. As placental transporters can be impacted by both HIV infection and drug therapy, our objective was to explore the impact of HIV infection and cART on transporter expression. Drug transporter expression was examined in human placental samples collected from women with HIV (n = 25) and from healthy HIV(-) controls (n = 23). The effect of exposure to drugs commonly used in cART during pregnancy was examined in vitro in placental villous explants obtained from healthy women. Gene expression was measured via qRT-PCR. Several ABC (ABCG2, ABCC1,2,4) and SLC (SLC21A9, SLC22A1,3,11) transporters were significantly downregulated in placentas isolated from HIV(+) women as compared with HIV(-) controls (p < 0.05-0.001), while ABCB1 and SLC21A12 were significantly upregulated (p < 0.001). Twenty-four to 48-h exposure of human placental explants to agents used in cART resulted in significant upregulation of ABCB1 and downregulation of SLC22A11. Our findings suggest that transplacental transport may be compromised during HIV infection due to altered expression of clinically important transporters. Furthermore, in vitro results indicate that cART imposes significant alterations in placental transporters but not all changes are consistent with findings in the placenta from HIV(+) women, indicating disease effects. As this may impact in utero-fetal exposure to clinically used medications, further studies are needed to determine the overall impact on maternal-fetal transfer.

Identifiants

pubmed: 33099683
doi: 10.1208/s12248-020-00516-2
pii: 10.1208/s12248-020-00516-2
doi:

Substances chimiques

ATP-Binding Cassette Transporters 0
Anti-HIV Agents 0
Organic Anion Transporters 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

138

Subventions

Organisme : CIHR
ID : MOP 13346
Pays : Canada
Organisme : CIHR
ID : MOP-130398
Pays : Canada
Organisme : CIHR
ID : PJT-148684
Pays : Canada

Auteurs

Dea Kojovic (D)

Leslie Dan Faculty of Pharmacy, University of Toronto, 144 College Street, Toronto, Ontario, M5S 3M2, Canada.

Ragia H Ghoneim (RH)

Pharmacy Practice Department, Faculty of Pharmacy, King Abdulaziz University, Jeddah, Saudi Arabia.

Lena Serghides (L)

Toronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada.
Department of Immunology and Institute of Medical Sciences, Faculty of Medicine, University of Toronto, Toronto, Ontario, Canada.

Micheline Piquette-Miller (M)

Leslie Dan Faculty of Pharmacy, University of Toronto, 144 College Street, Toronto, Ontario, M5S 3M2, Canada. m.piquette.miller@utoronto.ca.

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Classifications MeSH