Evidence map›Paper›PMID 40988542›Full record

ArticleThe Journal of infectious diseases2026

Maternal Inflammation Likely Drives Impaired Immune Responses to Respiratory Syncytial Virus in HIV-Exposed Uninfected Infants.

Christiana Smith, Kaili Curtis, Adrianne Bonham, Shea Boyer, Kacey Navarro, Joyce Fu, Nicole Larrea, Judith C Shlay, Laurel L Lenz, Adriana Weinberg

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Christiana SmithDepartment of Pediatrics, Medicine, and Pathology, University of Colorado, Aurora, Colorado, USA.ORCID 0000-0002-4611-6477
Kaili CurtisDepartment of Pediatrics, Medicine, and Pathology, University of Colorado, Aurora, Colorado, USA.ORCID 0009-0006-9922-2499
Adrianne BonhamDepartment of Pediatrics, Medicine, and Pathology, University of Colorado, Aurora, Colorado, USA.
Shea BoyerDepartment of Pediatrics, Medicine, and Pathology, University of Colorado, Aurora, Colorado, USA.
Kacey NavarroDepartment of Pediatrics, Medicine, and Pathology, University of Colorado, Aurora, Colorado, USA.
Joyce FuDepartment of Obstetrics and Gynecology, University of Colorado, Aurora, Colorado, USA.
Nicole LarreaDepartment of Obstetrics and Gynecology, Denver Health and Hospitals Authority, Denver, Colorado, USA.ORCID 0000-0003-4714-8945
Judith C ShlayPublic Health Institute at Denver Health, Denver Health and Hospital Authority, Denver, Colorado, USA.ORCID 0000-0002-9494-439X
Laurel L LenzDepartment of Immunology and Microbiology, University of Colorado, Aurora, Colorado, USA.
Adriana WeinbergDepartment of Pediatrics, Medicine, and Pathology, University of Colorado, Aurora, Colorado, USA.ORCID 0000-0001-6920-0623

Funding

NIH Prior Approval Process ProfessionalUL1TR002535 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2018 to 2022
$51.1M
Colorado Clinical and Translational Sciences Institute (CCTSI)UM1TR004399 · NCATS · UNIVERSITY OF COLORADO DENVER · PI JANINE A HIGGINS, RONALD J. SOKOL · 2023 to 2026
$30.7M
Dendritic cell targeting by bacterial LysM proteins to suppress inflammationR01AI178925 · NIAID · UNIVERSITY OF COLORADO DENVER · PI Laurel L Lenz · 2023 to 2026
$1.9M
Innate Immune Defects in HIV-Exposed Uninfected Infants: Effect on Respiratory Syncytial Virus InfectionK08HD100205 · NICHD · UNIVERSITY OF COLORADO DENVER · PI SMITH-ANDERSON, CHRISTIANA ELIZABETH · 2020 to 2024
$810k
Doris Duke Charitable FoundationNational Institute of Child Health and Human DevelopmentNCATS NIH HHSNCATS NIH HHS UL1 TR002535NCATS NIH HHS UM1 TR004399NIAID NIH HHS R01 AI178925NICHD NIH HHS K08 HD100205NIH HHSNIH HHS 1K08HD100205University of Colorado School of Medicine
6 · The paper itself

Abstract

backgroundRespiratory syncytial virus (RSV) is the leading cause of lower respiratory tract infection and a major contributor to morbidity and mortality in HIV-exposed, uninfected (HEU) infants. The mechanisms underlying HEU infants' increased susceptibility to RSV are unclear.

methodsWe recruited pregnant women with and without HIV, plus HEU and HIV-unexposed (HUU) children at 12-18 months of age and collected peripheral and cord blood. We measured innate immune responses of infants to RSV using an in vitro model of human respiratory infection. These responses were correlated with markers of inflammation in maternal and cord blood. We also incubated HUU cord blood cells in plasma from women living with HIV (WLHIV) to recapitulate the RSV-specific responses in HEU cord blood cells.

resultsWe enrolled 30 WLHIV, 61 HIV-negative women, 19 HEU and 20 HUU children. At birth, HEU infants demonstrated lower expression of IL-12 by dendritic cells (P < .0001) and IFNγ by natural killer (NK) cells (P = .007); the difference in IL-12 expression persisted to 12-18 months of age (P = .015). WLHIV had high concentrations of multiple inflammatory molecules in peripheral blood; these correlated inversely with infant RSV-specific immune responses. Incubation of cord blood cells from HUU infants in maternal plasma from WLHIV significantly lowered RSV-specific NK cytotoxicity and antigen-presenting cell activation compared to incubation in HIV-negative maternal plasma.

conclusionsMaternal inflammation is a likely driver of innate immune dysregulation in HEU infants and predisposes to an increased susceptibility to RSV infection.

Indexed as

HIV InfectionsInflammationPregnancy Complications, InfectiousRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsAdultDendritic CellsFemaleFetal BloodHumansImmunity, InnateInfantInfant, NewbornKiller Cells, NaturalMalePregnancydendritic cellHIV-exposed uninfected infantinnate immune responsenatural killer cellrespiratory syncytial virus

Identifiers

PMID40988542
PMCPMC12951713

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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.