Evidence map›Paper›PMID 36649247›Full record

ArticlePloS one2023

HIV and SARS-CoV-2 infection in postpartum Kenyan women and their infants.

Emily R Begnel, Bhavna H Chohan, Ednah Ojee, Judith Adhiambo, Prestone Owiti, Vincent Ogweno, LaRinda A Holland, Carolyn S Fish, Barbra A Richardson, Adam K Khan and 8 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.4field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 10 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 6 institutions in 3 countries.

Emily R BegnelDepartment of Global Health, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0003-3491-7303
Bhavna H ChohanDepartment of Global Health, University of Washington, Seattle, Washington, United States of America.
Ednah OjeeDepartment of Paediatrics and Child Health, University of Nairobi, Nairobi, Kenya.
Judith AdhiamboDepartment of Paediatrics and Child Health, University of Nairobi, Nairobi, Kenya.
Prestone OwitiDepartment of Paediatrics and Child Health, University of Nairobi, Nairobi, Kenya.
Vincent OgwenoDepartment of Paediatrics and Child Health, University of Nairobi, Nairobi, Kenya.
LaRinda A HollandCenter for Fundamental and Applied Microbiomics, Biodesign Institute, Arizona State University, Tempe, Arizona, United States of America.
Carolyn S FishDivision of Human Biology, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.
Barbra A RichardsonDepartment of Global Health, University of Washington, Seattle, Washington, United States of America.
Adam K KhanSchool of Life Sciences, Arizona State University, Tempe, Arizona, United States of America.
Rabia MaqsoodCenter for Fundamental and Applied Microbiomics, Biodesign Institute, Arizona State University, Tempe, Arizona, United States of America.
Efrem S LimCenter for Fundamental and Applied Microbiomics, Biodesign Institute, Arizona State University, Tempe, Arizona, United States of America.
Manish SadaranganiVaccine Evaluation Center, BC Children's Hospital Research Institute, Vancouver, British Columbia, Canada.ORCID 0000-0002-9985-6452
Dara A LehmanDepartment of Global Health, University of Washington, Seattle, Washington, United States of America.ORCID 0000-0002-0372-0631
Jennifer SlykerDepartment of Global Health, University of Washington, Seattle, Washington, United States of America.
John KinuthiaDepartment of Global Health, University of Washington, Seattle, Washington, United States of America.
Dalton WamalwaDepartment of Global Health, University of Washington, Seattle, Washington, United States of America.
Soren GanttDépartement de Microbiologie, Infectiologie et Immunologie, Université de Montréal, Centre de Recherche du CHU St-Justine, Montréal, Québec, Canada.
University of Washington · USUniversity of Nairobi · KEArizona State University · USFred Hutch Cancer Center · USUniversité de Montréal · CAUniversity of British Columbia · CA

Funding

Maternal-infant Virome Transmission: the role of HIV and Antiretroviral TherapyR01HD092311 · NICHD · FRED HUTCHINSON CANCER RESEARCH CENTER · PI LEHMAN, DARA ANN · 2017 to 2021
$3.9M
The Virome and Microbiome in Health and BK Disease of Kidney Transplant PatientsR00DK107923 · NIDDK · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI LIM, EFREM · 2017 to 2019
$747k
Medical Research Council MC_PC_17221Medical Research Council MR/R005990/1Medical Research Council MR/R005990/2NICHD NIH HHS R01 HD092311NIDDK NIH HHS R00 DK107923
6 · The paper itself

Abstract

backgroundHIV may increase SARS-CoV-2 infection risk and COVID-19 severity generally, but data are limited about its impact on postpartum women and their infants. As such, we characterized SARS-CoV-2 infection among mother-infant pairs in Nairobi, Kenya.

methodsWe conducted a nested study of 62 HIV-uninfected and 64 healthy women living with HIV, as well as their HIV-exposed uninfected (N = 61) and HIV-unexposed (N = 64) infants, participating in a prospective cohort. SARS-CoV-2 serology was performed on plasma collected between May 1, 2020-February 1, 2022 to determine the incidence, risk factors, and symptoms of infection. SARS-CoV-2 RNA PCR and sequencing was also performed on available stool samples from seropositive participants.

resultsSARS-CoV-2 seropositivity was found in 66% of the 126 mothers and in 44% of the 125 infants. There was no significant association between SARS-CoV-2 infection and maternal HIV (Hazard Ratio [HR] = 0.810, 95% CI: 0.517-1.27) or infant HIV exposure (HR = 1.47, 95% CI: 0.859-2.53). Maternal SARS-CoV-2 was associated with a two-fold increased risk of infant infection (HR = 2.31, 95% CI: 1.08-4.94). Few participants (13% mothers, 33% infants) had symptoms; no participant experienced severe COVID-19 or death. Seroreversion occurred in about half of mothers and infants. SARS-CoV-2 sequences obtained from stool were related to contemporaneously circulating variants.

conclusionsThese data indicate that postpartum Kenyan women and their infants were at high risk for SARS-CoV-2 infection and that antibody responses waned over an average of 8-10 months. However, most cases were asymptomatic and healthy women living with HIV did not have a substantially increased risk of infection or severe COVID-19.

Indexed as

COVID-19HIV InfectionsCase-Control StudiesFecesFemaleHumansInfantKenyaPolymerase Chain ReactionPostpartum PeriodProspective StudiesRNA, ViralSARS-CoV-2RNA, Viral

Identifiers

PMID36649247
PMCPMC9844875
OpenAlexW4316928395

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.