Evidence map›Paper›PMID 41890730›Full record

ArticleFrontiers in immunology2026

Gestational and lactational exposure to HIV tri-combination therapy induces sex- and dose-dependent changes in inflammatory cytokine profiles, intestinal permeability, and villi morphology in adult rat offspring.

Yaswanthi Yanamadala, Kuppan Gokulan, Kumari Karn, Vicki Sutherland, Helen Cunny, Janine H Santos, Kelly Davis, Sangeeta Khare

Abstract read
In one paragraph

Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Yaswanthi YanamadalaDivision of Microbiology, National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR, United States.
Kuppan GokulanDivision of Microbiology, National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR, United States.
Kumari KarnDivision of Microbiology, National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR, United States.
Vicki SutherlandDivision of Translational Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, NC, United States.
Helen CunnyDivision of Translational Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, NC, United States.
Janine H SantosDivision of Translational Toxicology, National Institute of Environmental Health Sciences, Research Triangle Park, NC, United States.
Kelly DavisToxicologic Pathology Associates, Jefferson, AR, United States.
Sangeeta KhareDivision of Microbiology, National Center for Toxicological Research, US Food and Drug Administration, Jefferson, AR, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Gestational antiretroviral therapy (ART) has significantly reduced the risk of vertical transmission of HIV, but concerns linger about its long-term effects on the fetal immune system and intestinal health. Our previous work has demonstrated dose-dependent changes in the fecal and mucosa-associated microbiome of adult rat offspring perinatally exposed to TC-ART (tri-combination ART: dolutegravir, abacavir, and lamivudine). These changes may either be driven by alterations in immune system and intestinal barrier integrity or potentially impact them. Methods: In this study, we further investigated the long-term effects of perinatal TC-ART exposure on intestinal permeability, cytokine profiles, and intestinal mucosa morphology. Results: We observed statistically significant sex-dependent differences, with male offspring exhibiting reduced weight gain, a dichotomous response between low and high dose for inflammatory cytokines [interleukin-5 (IL-5), IL-7, and IL-12], differential regulation for the mRNA expression of intestinal permeability-related genes (21 downregulated), and disrupted villous architecture, while females showed dose-dependent decreases in inflammatory cytokines [IL-17, IL-5, and macrophage colony-stimulating factor (M-CSF)]. In females, while some intestinal permeability genes were downregulated, the upregulation of other permeability genes suggests a compensatory mechanism to maintain the intestinal barrier function, indicating an overall milder response to TC-ART. Discussion: These findings suggest that perinatal exposure to TC-ART may have differential impacts on intestinal health, with females exhibiting a more adaptive response compared to males, highlighting the need for sex-specific considerations in evaluating long-term effects of ART.

Indexed as

Anti-HIV AgentsCytokinesHIV InfectionsIntestinal MucosaPrenatal Exposure Delayed EffectsAnimalsFemaleIntestinal Barrier FunctionLactationMaleMaternal ExposurePermeabilityPregnancyRatsSex FactorsAnti-HIV AgentsCytokinescytokinegene expressiongestational exposureHIVintestinal permeability

Identifiers

PMID41890730
PMCPMC13013449

What Socratic 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 Socratic graph.