Evidence map›Paper›PMID 41537918›Full record

ArticleVeterinary research communications2026

Effects of cecropin A on cytokine production and tight junction protein expression in chicken ileal explant cultures.

Rege Anna Márton, Olivér Varga, Naveen Joseph Vincent, Patrik Tráj, Csilla Sebők, Ágnes Kemény, Máté Mackei, Zsuzsanna Neogrády, Viviána Molnár-Nagy, Gábor Mátis

Abstract read
In one paragraph

Article in Veterinary research communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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.

Rege Anna MártonDepartment of Physiology and Biochemistry, University of Veterinary Medicine, István Street 2., Budapest, H-1078, Hungary. marton.rege.anna@univet.hu.
Olivér VargaDepartment of Physiology and Biochemistry, University of Veterinary Medicine, István Street 2., Budapest, H-1078, Hungary.
Naveen Joseph VincentDepartment of Physiology and Biochemistry, University of Veterinary Medicine, István Street 2., Budapest, H-1078, Hungary.
Patrik TrájDepartment of Physiology and Biochemistry, University of Veterinary Medicine, István Street 2., Budapest, H-1078, Hungary.
Csilla SebőkDepartment of Physiology and Biochemistry, University of Veterinary Medicine, István Street 2., Budapest, H-1078, Hungary.
Ágnes KeményDepartment of Physiology and Biochemistry, University of Veterinary Medicine, István Street 2., Budapest, H-1078, Hungary.
Máté MackeiDepartment of Physiology and Biochemistry, University of Veterinary Medicine, István Street 2., Budapest, H-1078, Hungary.
Zsuzsanna NeográdyDepartment of Physiology and Biochemistry, University of Veterinary Medicine, István Street 2., Budapest, H-1078, Hungary.
Viviána Molnár-NagyDr. Bata Ltd., Bajcsy-Zsilinszky Street 139., Ócsa, H-2364, Hungary.
Gábor MátisDepartment of Physiology and Biochemistry, University of Veterinary Medicine, István Street 2., Budapest, H-1078, Hungary.

Funding

Hungarian National Research, Development and Innovation Office grant number: OTKA FK 134940Ministry of Culture and Innovation of Hungary Project number 2023-2.1.2-KDP-2023-00007
6 · The paper itself

Abstract

In an era of antimicrobial resistance (AMR), identifying alternatives to conventional antibiotics in livestock farming is vital for veterinary medicine and public health. Due to the constant exposure to pathogens and the need for optimal productivity, maintaining gut homeostasis is essential in poultry. Therefore, investigating antimicrobial alternatives that can support gut health is of key importance. Host defense peptides (HDPs) have been identified as promising candidates due to their beneficial effects on the gut; however, there is still much to clarify regarding the individual peptides' mechanism of action. In the present study, the HDP cecropin A (CecA) was applied to chicken-derived ex vivo ileal explant cultures to examine its impact on immune response and tight junction (TJ) protein expression. CecA was applied at 3.125 and 6.25 µg/mL concentrations, either alone (Cec-low and Cec-high) or in polyinosinic-polycytidylic acid (Poly I:C, 50 µg/mL)-induced inflammatory conditions (PI:C + Cec-low and PI:C + Cec-high). The experiment revealed that CecA had no impact on cell viability, as reflected by unchanged metabolic activity and extracellular lactate dehydrogenase activity. Regarding the immune state, Cec-high and PI:C + Cec-high increased the production of interleukin (IL)-2, whereas IL-6 concentration was decreased by PI:C + Cec-low treatment. Furthermore, Cec-high elevated the intracellular expression of the TJ protein claudin-3. In conclusion, CecA displayed immunomodulatory activity in chicken intestinal cells and supported epithelial integrity without exerting cytotoxic effects.

Indexed as

Antimicrobial Cationic PeptidesChickensCytokinesIleumTight Junction ProteinsAnimalsAntimicrobial Cationic Peptidescecropin ACytokinesTight Junction ProteinsCecropin AGut explant cultureHost defense peptideImmunomodulationPoultryTight junction protein

Identifiers

PMID41537918
PMCPMC12808300

What Socratic holds

Textmetadata
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.