(30 lines only) The World Health Organization recommends that all HIV-infected pregnant women receive lifelong antiretroviral therapy (ART) for prevention of mother-to-child transmission (PMTCT-ART, formerly Option B+). Pre-exposure prophylaxis (PrEP) is also recommended by the WHO for all HIV-uninfected pregnant women with a high risk of HIV acquisition. HIV treatment and prevention among special populations, including pregnant women, are also high priorities in the NIH?s HIV research Trans-Plan. As PMTCT-ART expands and PrEP rolls out globally, the likelihood of pregnant women on antiretrovirals (ARVs) will substantially increase. Little is known, however, about the degree of transfer of maternal ARVs to infants during pregnancy. Such information could be useful for identifying the optimal maternal ART regimens to use during pregnancy to maximize infant protection against HIV while minimizing potential toxicities. As a monitoring matrix, neonatal hair can successfully quantify prenatal exposure to maternal medications in utero over time. To date, hair analysis has not been harnessed to evaluate rates of maternal to infant ARV transfer. The proposed study aims to quantify maternal-to-infant transfer during pregnancy for a variety of ARVs by employing a novel pharmacokinetic evaluation using maternal and neonatal hair in an unprecedented cohort. We will use validated assays developed by our group to measure ARV levels in hair samples collected at birth from mother-infant pairs enrolled in the Surveillance Monitoring for ART Toxicities Study in HIV-uninfected Children Born to HIV-infected Women (SMARTT Study), a Pediatric HIV/AIDS Cohort Study (PHACS)-funded prospective study designed to evaluate the effects of ARV exposure on infants born to HIV-infected mothers in the U.S. Leveraging data from this important cohort, we will quantify the extent of mother-to-infant transfer of different ARVs in utero through a paired analysis of mother and neonate hair samples collected at infant delivery (Aim 1) using validated liquid chromatography/tandem mass spectrometry (LC-MS/MS)-based methods. We will further assess the extent of correlation between maternal and infant hair concentrations for each ARV (specifically, for tenofovir [TFV], emtricitabine [FTC], lopinavir [LPV], ritonavir [RTV], atazanavir [ATV], darunavir [DRV], raltegravir [RAL], dolutegravir [DTG], efavirenz [EFV] and nevirapine [NVP]).
In Aim 2, we will evaluate whether in utero mother- to-infant transfer of ARVs differs by type or class of ARV and determine whether others characteristics influence the degree of transfer including duration of ARV use, concomitant medications, maternal CD4 count and HIV RNA level during pregnancy, and use of substances, psychotropic medications, or alcohol during pregnancy. We are uniquely positioned in this application to conduct these aims by leveraging an existing repository of collected hair samples from the SMARTT Study among mother-infant pairs. Our results will improve understanding of maternal-to-infant transfer for common ARVs used during pregnancy with ultimate implications for worldwide efforts to prevent perinatal HIV transmission with maximum efficacy and minimal toxicity.

Public Health Relevance

Although the use of HIV medications (antiretrovirals, ARVs) by mothers during pregnancy is a key strategy for the prevention of maternal to child transmission (PMTCT) of HIV infection, very little is known about the degree of transfer of ARVs from mother to baby during pregnancy. Using hair samples collected at the delivery visit in an important NIH-funded cohort (Surveillance Monitoring for ART Toxicities Study in HIV-uninfected Children Born to HIV-infected Women, SMARTT), we will perform an innovative study to examine the degree of transfer of various ARVs and ARV classes from mother to baby during pregnancy by analyzing ARV concentrations in hair. The ultimate goal of this study is to help determine which HIV regimens to use during pregnancy for HIV- positive mothers to maximize protection to the baby and mother, while minimizing toxicities to the infant.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Exploratory/Developmental Grants (R21)
Project #
1R21AI138618-01
Application #
9555849
Study Section
AIDS Clinical Studies and Epidemiology Study Section (ACE)
Program Officer
Miller, Judith A
Project Start
2018-06-06
Project End
2020-05-31
Budget Start
2018-06-06
Budget End
2019-05-31
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Washington
Department
Public Health & Prev Medicine
Type
Schools of Public Health
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195