Evidence map›Paper›PMID 40231720›Full record

RevieweLife2025

Coevolutionary interplay: Helminths-trained immunity and its impact on the rise of inflammatory diseases.

Eugenio Antonio Carrera Silva, Juliana Puyssegur, Andrea Emilse Errasti

Abstract readReview
In one paragraph

Review in eLife, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Anisakiasis: A Decade of Molecular and Diagnostic Advancements (2015-2026).International journal of molecular sciences · 2026
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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

3 authors.

Eugenio Antonio Carrera SilvaEACS and JP Institute of Experimental Medicine, National Scientific and Technical Research Council, National Academy of Medicine (IMEX-CONICET-ANM), Buenos Aires, Argentina.ORCID https://orcid.org/0000-0003-4428-8213
Juliana PuyssegurEACS and JP Institute of Experimental Medicine, National Scientific and Technical Research Council, National Academy of Medicine (IMEX-CONICET-ANM), Buenos Aires, Argentina.ORCID https://orcid.org/0009-0006-3326-272X
Andrea Emilse ErrastiAEE Institute of Pharmacology, School of Medicine, University of Buenos Aires, Buenos Aires, Argentina.ORCID https://orcid.org/0000-0003-2384-775X

Funding

Agencia Nacional de Promoción de la Investigación, el Desarrollo Tecnológico y la Innovación (ANPCyT); Fondo para la Investigación Científica y Tecnológica (FONCYT), Argentina. PICT-2021-I-A-00807Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Argentina PIP 2022-0763Fundación Florencio Fiorini, Argentina Fiorini 2024
6 · The paper itself

Abstract

The gut biome, a complex ecosystem of micro- and macro-organisms, plays a crucial role in human health. A disruption in this evolutive balance, particularly during early life, can lead to immune dysregulation and inflammatory disorders. 'Biome repletion' has emerged as a potential therapeutic approach, introducing live microbes or helminth-derived products to restore immune balance. While helminth therapy has shown some promise, significant challenges remain in optimizing clinical trials. Factors such as patient genetics, disease status, helminth species, and the optimal timing and dosage of their products or metabolites must be carefully considered to train the immune system effectively. We aim to discuss how helminths and their products induce trained immunity as prospective to treat inflammatory and autoimmune diseases. The molecular repertoire of helminth excretory/secretory products (ESPs), which includes proteins, peptides, lipids, and RNA-carrying extracellular vesicles (EVs), underscores their potential to modulate innate immune cells and hematopoietic stem cell precursors. Mimicking natural delivery mechanisms like synthetic exosomes could revolutionize EV-based therapies and optimizing production and delivery of ESP will be crucial for their translation into clinical applications. By deciphering and harnessing helminth-derived products' diverse modes of action, we can unleash their full therapeutic potential and pave the way for innovative treatments.

Indexed as

Autoimmune DiseasesHelminthsImmunity, InnateInflammationAnimalsHumansTherapy with HelminthsTrained ImmunityESPsEVsexcretory/secretory productsextracelular vesiclesgut biomehelminthsimmunologyinflammationinflammatory disorderstrained immunity

Identifiers

PMID40231720
PMCPMC12002795

What Socratic 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 Socratic graph.