Evidence map›Paper›PMID 41543350›Full record

ArticleMolecular nutrition & food research2026

Anti-Inflammatory Properties of Ripe and Unripe Papaya Pectin in a Neonatal Human Stem Cell-Derived Ileum Model.

Janaina Lombello Santos Donadio, João Paulo Fabi, Helena M Crowley, Marcelo B Sztein, Rosângela Salerno-Gonçalves

Abstract read
In one paragraph

Article in Molecular nutrition & food research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Janaina Lombello Santos DonadioCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, Maryland, USA.
João Paulo FabiFood Research Center (FoRC), CEPID-FAPESP (Research, Innovation and Dissemination Centers, São Paulo Research Foundation), CEPIX-USP, São Paulo, Brazil.
Helena M CrowleyDivision of Pediatric Surgery and Urology, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Marcelo B SzteinCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Rosângela Salerno-GonçalvesCenter for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore, Maryland, USA.

Funding

UNIVERSITY OF MARYLAND GREENEBAUM CANCER CENTERSUPPORT GRANTP30CA134274 · NCI · UNIVERSITY OF MARYLAND BALTIMORE · PI Xuefang Cao · 2008 to 2026
$51.0M
IMMUNE MECHANISMS OF PROTECTION IN S TYPHI VACCINESR01AI036525 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Marcelo B. Sztein · 1994 to 2026
$12.2M
Systems Biology and Biostatistics CoreU19AI181108 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Rosangela Mezghanni · 2024 to 2026
$8.0M
National Cancer Institute Cancer Center Support Grant (CCSG) P30CA134274NCI NIH HHS P30 CA134274NIAID, NIH, DHHS federal research U19 AI 181108NIAID NIH HHS R01 AI036525NIAID NIH HHS U19 AI181108Richard Schwartz Award for Excellence in Children's Health Research, Department of Pediatrics, UMB (JLSD and RSG), and Sao Paulo Research Foundation (FAPESP) scholarships to JLSD 2019/018794-0Richard Schwartz Award for Excellence in Children's Health Research, Department of Pediatrics, UMB (JLSD and RSG), and Sao Paulo Research Foundation (FAPESP) scholarships to JLSD 2021/07292-3
6 · The paper itself

Abstract

Pectin, a dietary fiber found in fruits and vegetables, has recognized anti-inflammatory properties. While papaya is rich in pectin, the impact of different ripening stages on its anti-inflammatory effects within the human neonatal gastrointestinal tract remains unexplored. Ripe and unripe papaya contain structurally distinct pectins, potentially leading to differing anti-inflammatory effects. Herein, ripe and unripe papaya pectins were tested in an in vitro model of human neonatal intestinal mucosa, in the presence or absence of commensal Escherichia coli (E. coli) as a surrogate for early intestinal colonizers. Papaya pectin enhanced cell viability regardless of ripening stage or the presence of E. coli. Both pectins reduced the IL-6 production in cultures exposed to E. coli, but only unripe pectin decreased IL-8 levels. Additionally, treatment with either pectin downregulated genes related to tight junctions and innate immune signaling (e.g., claudin-3, catenin-1, catenin-3, SUGT1, TRAF6, and NLRP3) in the presence of E. coli. Dimensionality reduction analyses further suggest that pectin induced distinct transcriptional profiles depending on the presence of bacteria. These results demonstrate that papaya pectin modulates epithelial barrier in a manner dependent on ripening stage and microbial context, providing novel insights into its functional and stage-specific anti-inflammatory activity.

Indexed as

Anti-Inflammatory AgentsCaricaIleumPectinsStem CellsCells, CulturedCell SurvivalEscherichia coliFruitHumansInfant, NewbornInterleukin-6Interleukin-8Intestinal MucosaAnti-Inflammatory AgentsInterleukin-6Interleukin-8Pectinsinflammationintestineneonatalpapayapectin

Identifiers

PMID41543350
PMCPMC13103872

What Socratic holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

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.