Evidence map›Paper›PMID 41097090›Full record

ArticleInternational journal of molecular sciences2025

An Innovative Immunotoxin Design Against Allergy Based on the IL-33 Cytokine and the Ribotoxin α-Sarcin.

Javier Narbona, Rodrigo Lázaro-Gorines, Adrián Gutiérrez-Carmona, Juan Carlos López-Rodríguez, Mayte Villalba, Javier Lacadena

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. 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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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Javier NarbonaDepartment of Biochemistry and Molecular Biology, Faculty of Chemical Sciences, Complutense University, 28040 Madrid, Spain.ORCID 0000-0002-6118-841X
Rodrigo Lázaro-GorinesCancer Immunotherapy Unit, Immunology Department, Hospital Universitario 12 Octubre, Avda. de Córdoba, s/n, 28041 Madrid, Spain.
Adrián Gutiérrez-CarmonaDepartment of Biochemistry and Molecular Biology, Faculty of Chemical Sciences, Complutense University, 28040 Madrid, Spain.
Juan Carlos López-RodríguezDepartamento de Ciencias Médicas Básicas, Facultad de Medicina, Instituto de Medicina Molecular Aplicada-Nemesio Díez (IMMA-ND), Universidad San Pablo-CEU, CEU Universities, Urbanización Montepríncipe, Ctra. Boadilla del Monte, Km. 5.300, 28668 Madrid, Spain.ORCID 0000-0002-6106-6551
Mayte VillalbaDepartment of Biochemistry and Molecular Biology, Faculty of Chemical Sciences, Complutense University, 28040 Madrid, Spain.ORCID 0000-0002-0042-9953
Javier LacadenaDepartment of Biochemistry and Molecular Biology, Faculty of Chemical Sciences, Complutense University, 28040 Madrid, Spain.ORCID 0000-0002-7314-0333

Funding

Ministerio de Ciencia, Innovación y Universidades PID2020-116692RB-I00
6 · The paper itself

Abstract

Allergies constitute one of the major health problems worldwide, increasing their prevalence in developed countries. To overcome this multifactorial disease, immunotherapy and the use of immune molecules, such as immunotoxins, have arisen as promising therapeutic tools. We have designed, produced, and characterized a new immunotoxin called IL-33αS, encompassing the murine IL-33 (mIL-33) as the target domain and the ribotoxin α-sarcin as the toxic domain. IL-33 is a widely described alarmin that binds to the ST2 receptor of a variety of immune cells, including ILC2s, leading to Th2-derived inflammatory response, as occurs in allergic reactions. Both IL-33αS and mIL-33 were successfully produced in the methylotrophic yeast

Indexed as

HypersensitivityImmunotoxinsInterleukin-33RibonucleasesAnimalsHumansInterleukin-1 Receptor-Like 1 ProteinMiceRAW 264.7 CellsTh2 CellsIl33 protein, mouseImmunotoxinsInterleukin-1 Receptor-Like 1 ProteinInterleukin-33Ribonucleasesallergic responseIL-33ILC2 cellsimmunotoxinribotoxin α-sarcinST2 receptor

Identifiers

PMID41097090
PMCPMC12525494

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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.