Evidence map›Paper›PMID 41781415›Full record

SynthesisScientific reports2026

The immune-modulatory potential of helminth-derived proteins in cellular models of inflammation: a systematic review with cross-study quantitative data analysis.

Sienna Stucke, Aonghus Feeney, Richard Lalor, Sheila Donnelly, John Pius Dalton, Declan McKernan, Eilís Dowd

Abstract readSystematic Review
In one paragraph

Synthesis in Scientific reports, 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. Review
  2. Association betweenFrontiers in immunology · 2026
    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

7 authors.

Sienna StuckePharmacology & Therapeutics, Galway Neuroscience Centre, Institute for Health Discovery and Innovation, School of Pharmacy and Medical Sciences, University of Galway, Galway, Ireland.
Aonghus FeeneyPharmacology & Therapeutics, Galway Neuroscience Centre, Institute for Health Discovery and Innovation, School of Pharmacy and Medical Sciences, University of Galway, Galway, Ireland.
Richard LalorMolecular Parasitology Laboratory, Centre for One Health, Ryan Institute, School of Natural Sciences, University of Galway, Galway, Ireland.
Sheila DonnellyMolecular Parasitology Laboratory, Centre for One Health, Ryan Institute, School of Natural Sciences, University of Galway, Galway, Ireland.
John Pius DaltonMolecular Parasitology Laboratory, Centre for One Health, Ryan Institute, School of Natural Sciences, University of Galway, Galway, Ireland.
Declan McKernanPharmacology & Therapeutics, Galway Neuroscience Centre, Institute for Health Discovery and Innovation, School of Pharmacy and Medical Sciences, University of Galway, Galway, Ireland.
Eilís DowdPharmacology & Therapeutics, Galway Neuroscience Centre, Institute for Health Discovery and Innovation, School of Pharmacy and Medical Sciences, University of Galway, Galway, Ireland. eilis.dowd@universityofgalway.ie.

Funding

Michael J Fox Foundation 17244 and 023410
6 · The paper itself

Abstract

Helminths are parasitic worms that secrete a plethora of immune regulatory molecules which allow them to moderate inflammatory responses by their host's immune system to ensure their survival within the host. This ability to drive a compatible existence with their host has led to research into the potential therapeutic effects of helminth-derived molecules the regulation of overactive immune and inflammatory responses in a wide variety of diseases. This systematic review with cross-study quantitative data analysis aims to synthesize the published data on helminth-derived immunomodulatory peptides/polypeptides/proteins (HDIPs) with a focus on determining the extent to which they modulate the inflammatory response in in vitro cellular models of inflammation. In accordance with PRISMA 2020 guidelines, a predefined systematic search of the PubMed, Web of Science and Medline databases identified relevant studies published up to September 2025, and 79 articles were included after screening. We found that most published studies used LPS or Concanavalin A stimulated macrophages, peripheral blood mononuclear cells or dendritic cells as the cellular model of inflammation. Twenty helminth species from which > 60 isolated HDIPs were derived were tested in these models, with the nematodes, Haemonchus contortus and Acanthocheilonema viteae, and the trematode, Fasciola hepatica, the most explored species. A common property of these molecules was the ability to significantly reduce the expression or production of pro-inflammatory cytokines such as IL-12, IL-1β, IL-6 and TNF, and significantly increase the expression or production of anti-inflammatory cytokines such as IL-10, TGFβ and IL-4. The effects on other cytokines, including IFNγ which is known to have both pro- and anti-inflammatory effects, were less consistent, with HDIPs either decreasing or increasing the levels of this cytokine. This systematic review with cross-study quantitative data analysis synthesizes the existing literature in this field and shows that the HDIPs secreted by several helminth species have consistently demonstrated effects though modification of cytokine levels and, as such, have therapeutic potential in conditions in which overactive immune and inflammatory responses play a pathogenic role.

Indexed as

Helminth ProteinsHelminthsInflammationAnimalsCytokinesHumansMacrophagesCytokinesHelminth ProteinsCytokinesHelminthHelminth-derived peptidesInflammationParasitic worms

Identifiers

PMID41781415
PMCPMC13069012

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.