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Interleukin-25-mediated resistance against intestinal trematodes does not depend on the generation of Th2 responses

BACKGROUND: The cytokine interleukin-25 (IL-25) is recognized as the most relevant initiator of protective T helper 2 (Th2) responses in intestinal helminth infections. This cytokine induces resistance against several species of intestinal helminths, including the trematode Echinostoma caproni. E. c...

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Autores principales: Álvarez-Izquierdo, María, Pérez-Crespo, Miguel, Esteban, J. Guillermo, Muñoz-Antoli, Carla, Toledo, Rafael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716497/
https://www.ncbi.nlm.nih.gov/pubmed/33276813
http://dx.doi.org/10.1186/s13071-020-04467-7
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author Álvarez-Izquierdo, María
Pérez-Crespo, Miguel
Esteban, J. Guillermo
Muñoz-Antoli, Carla
Toledo, Rafael
author_facet Álvarez-Izquierdo, María
Pérez-Crespo, Miguel
Esteban, J. Guillermo
Muñoz-Antoli, Carla
Toledo, Rafael
author_sort Álvarez-Izquierdo, María
collection PubMed
description BACKGROUND: The cytokine interleukin-25 (IL-25) is recognized as the most relevant initiator of protective T helper 2 (Th2) responses in intestinal helminth infections. This cytokine induces resistance against several species of intestinal helminths, including the trematode Echinostoma caproni. E. caproni has been extensively used as an experimental model to study the factors determining resistance to intestinal infections. In the study reported here, we assessed the role of IL-25 in the generation of resistance in mice infected with E. caproni. METHODS: The factors that determine the production of IL-25 in mice experimentally infected with E. caproni were determined, as were the consequences of IL-25 production in terms of polarization of the immune response and resistance to infection. RESULTS: Our results show that the role of IL-25 in the polarization of the immune response differs between the primary and secondary immune responses. IL-25 is required for the development of a Th2 phenotype in primary E. caproni infections, but it can also promote the differentiation to Th2 memory cell subsets that enhance type-2 immunity in memory responses. However, the development of Th2 responses does not induce resistance to infection. The Th2 phenotype does not elicit resistance, and IL-25 is responsible for the resistance regardless of its type-2 cytokine activity and activation of signal transducer and activator of transcription (STAT6). Alternative activation of macrophages induced by IL-25 can be implicated in the resistance to infection. CONCLUSIONS: In contrast to primary infection, secondary infection elicits a type-2 immune response even in the absence of IL-25 expression. Despite the development of a type-2 response, mice are susceptible to secondary infection associated with the lack of IL-25. Resistance to infection is due to the production of IL-25, which acts autonomously from Th2 response in terms of parasite clearance. [Image: see text]
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spelling pubmed-77164972020-12-04 Interleukin-25-mediated resistance against intestinal trematodes does not depend on the generation of Th2 responses Álvarez-Izquierdo, María Pérez-Crespo, Miguel Esteban, J. Guillermo Muñoz-Antoli, Carla Toledo, Rafael Parasit Vectors Research BACKGROUND: The cytokine interleukin-25 (IL-25) is recognized as the most relevant initiator of protective T helper 2 (Th2) responses in intestinal helminth infections. This cytokine induces resistance against several species of intestinal helminths, including the trematode Echinostoma caproni. E. caproni has been extensively used as an experimental model to study the factors determining resistance to intestinal infections. In the study reported here, we assessed the role of IL-25 in the generation of resistance in mice infected with E. caproni. METHODS: The factors that determine the production of IL-25 in mice experimentally infected with E. caproni were determined, as were the consequences of IL-25 production in terms of polarization of the immune response and resistance to infection. RESULTS: Our results show that the role of IL-25 in the polarization of the immune response differs between the primary and secondary immune responses. IL-25 is required for the development of a Th2 phenotype in primary E. caproni infections, but it can also promote the differentiation to Th2 memory cell subsets that enhance type-2 immunity in memory responses. However, the development of Th2 responses does not induce resistance to infection. The Th2 phenotype does not elicit resistance, and IL-25 is responsible for the resistance regardless of its type-2 cytokine activity and activation of signal transducer and activator of transcription (STAT6). Alternative activation of macrophages induced by IL-25 can be implicated in the resistance to infection. CONCLUSIONS: In contrast to primary infection, secondary infection elicits a type-2 immune response even in the absence of IL-25 expression. Despite the development of a type-2 response, mice are susceptible to secondary infection associated with the lack of IL-25. Resistance to infection is due to the production of IL-25, which acts autonomously from Th2 response in terms of parasite clearance. [Image: see text] BioMed Central 2020-12-04 /pmc/articles/PMC7716497/ /pubmed/33276813 http://dx.doi.org/10.1186/s13071-020-04467-7 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Álvarez-Izquierdo, María
Pérez-Crespo, Miguel
Esteban, J. Guillermo
Muñoz-Antoli, Carla
Toledo, Rafael
Interleukin-25-mediated resistance against intestinal trematodes does not depend on the generation of Th2 responses
title Interleukin-25-mediated resistance against intestinal trematodes does not depend on the generation of Th2 responses
title_full Interleukin-25-mediated resistance against intestinal trematodes does not depend on the generation of Th2 responses
title_fullStr Interleukin-25-mediated resistance against intestinal trematodes does not depend on the generation of Th2 responses
title_full_unstemmed Interleukin-25-mediated resistance against intestinal trematodes does not depend on the generation of Th2 responses
title_short Interleukin-25-mediated resistance against intestinal trematodes does not depend on the generation of Th2 responses
title_sort interleukin-25-mediated resistance against intestinal trematodes does not depend on the generation of th2 responses
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7716497/
https://www.ncbi.nlm.nih.gov/pubmed/33276813
http://dx.doi.org/10.1186/s13071-020-04467-7
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