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IL-33-Mediated Protection against Experimental Cerebral Malaria Is Linked to Induction of Type 2 Innate Lymphoid Cells, M2 Macrophages and Regulatory T Cells

Cerebral malaria (CM) is a complex parasitic disease caused by Plasmodium sp. Failure to establish an appropriate balance between pro- and anti-inflammatory immune responses is believed to contribute to the development of cerebral pathology. Using the blood-stage PbA (Plasmodium berghei ANKA) model...

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Autores principales: Besnard, Anne-Gaelle, Guabiraba, Rodrigo, Niedbala, Wanda, Palomo, Jennifer, Reverchon, Flora, Shaw, Tovah N., Couper, Kevin N., Ryffel, Bernhard, Liew, Foo Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4450060/
https://www.ncbi.nlm.nih.gov/pubmed/25659095
http://dx.doi.org/10.1371/journal.ppat.1004607
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author Besnard, Anne-Gaelle
Guabiraba, Rodrigo
Niedbala, Wanda
Palomo, Jennifer
Reverchon, Flora
Shaw, Tovah N.
Couper, Kevin N.
Ryffel, Bernhard
Liew, Foo Y.
author_facet Besnard, Anne-Gaelle
Guabiraba, Rodrigo
Niedbala, Wanda
Palomo, Jennifer
Reverchon, Flora
Shaw, Tovah N.
Couper, Kevin N.
Ryffel, Bernhard
Liew, Foo Y.
author_sort Besnard, Anne-Gaelle
collection PubMed
description Cerebral malaria (CM) is a complex parasitic disease caused by Plasmodium sp. Failure to establish an appropriate balance between pro- and anti-inflammatory immune responses is believed to contribute to the development of cerebral pathology. Using the blood-stage PbA (Plasmodium berghei ANKA) model of infection, we show here that administration of the pro-Th2 cytokine, IL-33, prevents the development of experimental cerebral malaria (ECM) in C57BL/6 mice and reduces the production of inflammatory mediators IFN-γ, IL-12 and TNF-α. IL-33 drives the expansion of type-2 innate lymphoid cells (ILC2) that produce Type-2 cytokines (IL-4, IL-5 and IL-13), leading to the polarization of the anti-inflammatory M2 macrophages, which in turn expand Foxp3 regulatory T cells (Tregs). PbA-infected mice adoptively transferred with ILC2 have elevated frequency of M2 and Tregs and are protected from ECM. Importantly, IL-33-treated mice deleted of Tregs (DEREG mice) are no longer able to resist ECM. Our data therefore provide evidence that IL-33 can prevent the development of ECM by orchestrating a protective immune response via ILC2, M2 macrophages and Tregs.
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spelling pubmed-44500602015-06-23 IL-33-Mediated Protection against Experimental Cerebral Malaria Is Linked to Induction of Type 2 Innate Lymphoid Cells, M2 Macrophages and Regulatory T Cells Besnard, Anne-Gaelle Guabiraba, Rodrigo Niedbala, Wanda Palomo, Jennifer Reverchon, Flora Shaw, Tovah N. Couper, Kevin N. Ryffel, Bernhard Liew, Foo Y. PLoS Pathog Research Article Cerebral malaria (CM) is a complex parasitic disease caused by Plasmodium sp. Failure to establish an appropriate balance between pro- and anti-inflammatory immune responses is believed to contribute to the development of cerebral pathology. Using the blood-stage PbA (Plasmodium berghei ANKA) model of infection, we show here that administration of the pro-Th2 cytokine, IL-33, prevents the development of experimental cerebral malaria (ECM) in C57BL/6 mice and reduces the production of inflammatory mediators IFN-γ, IL-12 and TNF-α. IL-33 drives the expansion of type-2 innate lymphoid cells (ILC2) that produce Type-2 cytokines (IL-4, IL-5 and IL-13), leading to the polarization of the anti-inflammatory M2 macrophages, which in turn expand Foxp3 regulatory T cells (Tregs). PbA-infected mice adoptively transferred with ILC2 have elevated frequency of M2 and Tregs and are protected from ECM. Importantly, IL-33-treated mice deleted of Tregs (DEREG mice) are no longer able to resist ECM. Our data therefore provide evidence that IL-33 can prevent the development of ECM by orchestrating a protective immune response via ILC2, M2 macrophages and Tregs. Public Library of Science 2015-02-06 /pmc/articles/PMC4450060/ /pubmed/25659095 http://dx.doi.org/10.1371/journal.ppat.1004607 Text en © 2015 Besnard et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Besnard, Anne-Gaelle
Guabiraba, Rodrigo
Niedbala, Wanda
Palomo, Jennifer
Reverchon, Flora
Shaw, Tovah N.
Couper, Kevin N.
Ryffel, Bernhard
Liew, Foo Y.
IL-33-Mediated Protection against Experimental Cerebral Malaria Is Linked to Induction of Type 2 Innate Lymphoid Cells, M2 Macrophages and Regulatory T Cells
title IL-33-Mediated Protection against Experimental Cerebral Malaria Is Linked to Induction of Type 2 Innate Lymphoid Cells, M2 Macrophages and Regulatory T Cells
title_full IL-33-Mediated Protection against Experimental Cerebral Malaria Is Linked to Induction of Type 2 Innate Lymphoid Cells, M2 Macrophages and Regulatory T Cells
title_fullStr IL-33-Mediated Protection against Experimental Cerebral Malaria Is Linked to Induction of Type 2 Innate Lymphoid Cells, M2 Macrophages and Regulatory T Cells
title_full_unstemmed IL-33-Mediated Protection against Experimental Cerebral Malaria Is Linked to Induction of Type 2 Innate Lymphoid Cells, M2 Macrophages and Regulatory T Cells
title_short IL-33-Mediated Protection against Experimental Cerebral Malaria Is Linked to Induction of Type 2 Innate Lymphoid Cells, M2 Macrophages and Regulatory T Cells
title_sort il-33-mediated protection against experimental cerebral malaria is linked to induction of type 2 innate lymphoid cells, m2 macrophages and regulatory t cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4450060/
https://www.ncbi.nlm.nih.gov/pubmed/25659095
http://dx.doi.org/10.1371/journal.ppat.1004607
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