Evidence map›Paper›PMID 42209572›Full record

ArticleScientific reports2026

Polyclonal antibodies and probiotics improve immune dysfunction in a mouse model of inflammatory bowel disease.

Sirous Ghaedi, Zohreh Harsij, Maryam Dianati Rizi, Mehrdad Rezaei, Fatemeh Moein, Zahra Mirasadi, Nima Tanhaeivash, Nazanin Jamshidi, Mohammad Hossein Nasr-Esfahani, Mehdi Hajian

Abstract read
In one paragraph

Article in Scientific reports, 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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0cells of the map it votes in
0citing papers in PubMed
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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

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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

10 authors.

Sirous GhaediDepartment of Animal Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.
Zohreh HarsijDepartment of Biotechnology, Faculty of Biological Science and Technology, University of Isfahan, Isfahan, Iran.
Maryam Dianati RiziDepartment of Cell and Molecular Biology & Microbiology, Faculty of Biological Science & Technology, University of Isfahan, Isfahan, Iran.
Mehrdad RezaeiDepartment of Animal Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.
Fatemeh MoeinDepartment of Animal Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.
Zahra MirasadiDepartment of Animal Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.
Nima TanhaeivashDepartment of Animal Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.
Nazanin JamshidiDepartment of Animal Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.
Mohammad Hossein Nasr-EsfahaniDepartment of Animal Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.
Mehdi HajianDepartment of Animal Biotechnology, Reproductive Biomedicine Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran. m.hajian@royan-rc.ac.ir.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory bowel disease (IBD) is a chronic digestive disorder caused by the overactivity of the mucosal immune system in response to natural intestinal bacteria and environmental factors, affecting genetically susceptible individuals. This research investigates the preventive effect of probiotics (P), specifically Lactobacillus fermentum, Lactobacillus L. reuteri, and polyclonal antibodies (AB), on morphological changes and markers of intestinal inflammation in the IBD mice model. Our study spanned 54 days. For the first 21 days, we observed microbial populations and immunoglobulin levels. Then, we induced chronic inflammation over three 11-day cycles. In each cycle, subjects received 2% dextran sulfate sodium (DSS) for 4 days, followed by 7 days of normal water. 75 C57BL/6 mice have been used in 5 groups: DSS, control, DSS + P, DSS + AB, and a combined treatment group of antibodies and probiotics (DSS + ABP). Throughout the study period, clinical symptoms were monitored, and morphological changes and histological scores were assessed after the course. Levels of IBD biomarkers in serum such as nitrite, malondialdehyde enzyme (MDA), and myeloperoxidase enzyme (MPO), were measured along with alterations in cytokines Tumor Necrosis Factor-alpha (TNF-α), interleukin (IL)-4, IL-6, and IL-22, IgA and IgG in the blood serum. Results showed that All treatment groups, significantly reduced the Disease Activity Index (DAI), total histological score and oxidative stress markers MDA and MPO compared to the DSS group (p < 0.05). Additionally, the oral administration of polyclonal antibodies increased mucosal immunoglobulin levels, helping to prevent the rise in serum immunoglobulin levels and the associated increase in IL-4 (p < 0.05). Meanwhile, treatment with probiotics significantly (p < 0.05) reduced inflammation by modulating cytokine levels (TNF-α and IL-6). In conclusion, the co-administration of probiotics and polyclonal antibodies effectively mitigates IBD progression by synergistically improving histological parameters and regulating systemic immune responses, offering a more potent preventive strategy than individual treatments.

Indexed as

AntibodiesInflammatory Bowel DiseasesProbioticsAnimalsBiomarkersCytokinesDextran SulfateDisease Models, AnimalLimosilactobacillus fermentumLimosilactobacillus reuteriMaleMiceMice, Inbred C57BLPeroxidaseAntibodiesBiomarkersCytokinesDextran SulfatePeroxidaseIBD biomarkersImmunoglobulinsInflammatory bowel diseaseInterleukinsLactobacillus

Identifiers

PMID42209572
PMCPMC13448209

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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.