Evidence map›Paper›PMID 39769391›Full record

ArticleInternational journal of molecular sciences2024

Mucosal Bacterial Immunotherapy Attenuates the Development of Experimental Colitis by Reducing Inflammation Through the Regulation of Myeloid Cells.

Eva Jiménez, Alberto Vázquez, Sara González, Rosa Sacedón, Lidia M Fernández-Sevilla, Alberto Varas, Jose L Subiza, Jaris Valencia, Ángeles Vicente

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Pleiotropic Mucosal Innate Immune Memory in the Gastrointestinal Tract.International journal of molecular sciences · 2025
    Review
  3. Review
  4. Peptides Derived from α-Tubulin Induce Functional T Regulatory Cells.International journal of molecular sciences · 2025
    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

9 authors.

Eva JiménezDepartment of Cell Biology, Faculty of Medicine, UCM, 28040 Madrid, Spain.
Alberto VázquezDepartment of Cell Biology, Faculty of Medicine, UCM, 28040 Madrid, Spain.
Sara GonzálezDepartment of Cell Biology, Faculty of Medicine, UCM, 28040 Madrid, Spain.ORCID 0009-0003-5533-1894
Rosa SacedónDepartment of Cell Biology, Faculty of Medicine, UCM, 28040 Madrid, Spain.
Lidia M Fernández-SevillaHealth Research Institute of the Hospital Clínico San Carlos (IdISSC), 28040 Madrid, Spain.ORCID 0000-0003-0076-3254
Alberto VarasDepartment of Cell Biology, Faculty of Medicine, UCM, 28040 Madrid, Spain.ORCID 0000-0001-8329-6457
Jose L SubizaInmunotek S.L., Alcalá de Henares, 28805 Madrid, Spain.ORCID 0000-0002-0134-5321
Jaris ValenciaDepartment of Cell Biology, Faculty of Medicine, UCM, 28040 Madrid, Spain.ORCID 0000-0002-3112-5944
Ángeles VicenteDepartment of Cell Biology, Faculty of Medicine, UCM, 28040 Madrid, Spain.ORCID 0000-0002-9456-5541

Funding

Council of Science University and innovation; Community of Madrid IND2020/BMD-17358Instituto de Salud Carlos III co-funded by ERDF-Next Generation EU "Plan de Recuperación, Transformación y Resiliencia" RD21/0017/0010Spanish Ministry of Science and Innovation PID2021-123068OBI00/AEI/10.13039/501100011033/FEDER, UE
6 · The paper itself

Abstract

Ulcerative colitis is a chronic relapsing-remitting and potentially progressive form of inflammatory bowel disease in which there is extensive inflammation and mucosal damage in the colon and rectum as a result of an abnormal immune response. MV130 is a mucosal-trained immunity-based vaccine used to prevent respiratory tract infections in various clinical settings. Additionally, MV130 may induce innate immune cells that acquire anti-inflammatory properties and promote tolerance, which could have important implications for chronic inflammatory diseases such as ulcerative colitis. This work demonstrated that the prophylactic administration of MV130 substantially mitigated colitis in a mouse model of acute colitis induced by dextran sulphate sodium. MV130 downregulated systemic and local inflammatory responses, maintained the integrity of the intestinal barrier by preserving the enterocyte layer and goblet cells, and reduced the oedema and fibrosis characteristic of the disease. Mechanistically, MV130 significantly reduced the infiltration of neutrophils and pro-inflammatory macrophages in the intestinal wall of the diseased animals and favoured the appearance of M2-polarised macrophages. These results suggest that MV130 might have therapeutic potential for the treatment of ulcerative colitis, reducing the risk of relapse and the progression of disease.

Indexed as

Dextran SulfateDisease Models, AnimalImmunotherapyMyeloid CellsAnimalsColitisColitis, UlcerativeImmunity, MucosalInflammationIntestinal MucosaMacrophagesMiceMice, Inbred C57BLDextran Sulfatebacterial immunotherapyimmunomodulationinflammationmacrophagesMV130neutrophilsulcerative colitisvaccine

Identifiers

PMID39769391
PMCPMC11728189

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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 OpenQuestion graph.