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HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33
Infection by helminth parasites is associated with amelioration of allergic reactivity, but mechanistic insights into this association are lacking. Products secreted by the mouse parasite Heligmosomoides polygyrus suppress type 2 (allergic) immune responses through interference in the interleukin-33...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655542/ https://www.ncbi.nlm.nih.gov/pubmed/29045903 http://dx.doi.org/10.1016/j.immuni.2017.09.015 |
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author | Osbourn, Megan Soares, Dinesh C. Vacca, Francesco Cohen, E. Suzanne Scott, Ian C. Gregory, William F. Smyth, Danielle J. Toivakka, Matilda Kemter, Andrea M. le Bihan, Thierry Wear, Martin Hoving, Dennis Filbey, Kara J. Hewitson, James P. Henderson, Holly Gonzàlez-Cìscar, Andrea Errington, Claire Vermeren, Sonja Astier, Anne L. Wallace, William A. Schwarze, Jürgen Ivens, Alasdair C. Maizels, Rick M. McSorley, Henry J. |
author_facet | Osbourn, Megan Soares, Dinesh C. Vacca, Francesco Cohen, E. Suzanne Scott, Ian C. Gregory, William F. Smyth, Danielle J. Toivakka, Matilda Kemter, Andrea M. le Bihan, Thierry Wear, Martin Hoving, Dennis Filbey, Kara J. Hewitson, James P. Henderson, Holly Gonzàlez-Cìscar, Andrea Errington, Claire Vermeren, Sonja Astier, Anne L. Wallace, William A. Schwarze, Jürgen Ivens, Alasdair C. Maizels, Rick M. McSorley, Henry J. |
author_sort | Osbourn, Megan |
collection | PubMed |
description | Infection by helminth parasites is associated with amelioration of allergic reactivity, but mechanistic insights into this association are lacking. Products secreted by the mouse parasite Heligmosomoides polygyrus suppress type 2 (allergic) immune responses through interference in the interleukin-33 (IL-33) pathway. Here, we identified H. polygyrus Alarmin Release Inhibitor (HpARI), an IL-33-suppressive 26-kDa protein, containing three predicted complement control protein (CCP) modules. In vivo, recombinant HpARI abrogated IL-33, group 2 innate lymphoid cell (ILC2) and eosinophilic responses to Alternaria allergen administration, and diminished eosinophilic responses to Nippostrongylus brasiliensis, increasing parasite burden. HpARI bound directly to both mouse and human IL-33 (in the cytokine’s activated state) and also to nuclear DNA via its N-terminal CCP module pair (CCP1/2), tethering active IL-33 within necrotic cells, preventing its release, and forestalling initiation of type 2 allergic responses. Thus, HpARI employs a novel molecular strategy to suppress type 2 immunity in both infection and allergy. |
format | Online Article Text |
id | pubmed-5655542 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-56555422017-10-30 HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33 Osbourn, Megan Soares, Dinesh C. Vacca, Francesco Cohen, E. Suzanne Scott, Ian C. Gregory, William F. Smyth, Danielle J. Toivakka, Matilda Kemter, Andrea M. le Bihan, Thierry Wear, Martin Hoving, Dennis Filbey, Kara J. Hewitson, James P. Henderson, Holly Gonzàlez-Cìscar, Andrea Errington, Claire Vermeren, Sonja Astier, Anne L. Wallace, William A. Schwarze, Jürgen Ivens, Alasdair C. Maizels, Rick M. McSorley, Henry J. Immunity Article Infection by helminth parasites is associated with amelioration of allergic reactivity, but mechanistic insights into this association are lacking. Products secreted by the mouse parasite Heligmosomoides polygyrus suppress type 2 (allergic) immune responses through interference in the interleukin-33 (IL-33) pathway. Here, we identified H. polygyrus Alarmin Release Inhibitor (HpARI), an IL-33-suppressive 26-kDa protein, containing three predicted complement control protein (CCP) modules. In vivo, recombinant HpARI abrogated IL-33, group 2 innate lymphoid cell (ILC2) and eosinophilic responses to Alternaria allergen administration, and diminished eosinophilic responses to Nippostrongylus brasiliensis, increasing parasite burden. HpARI bound directly to both mouse and human IL-33 (in the cytokine’s activated state) and also to nuclear DNA via its N-terminal CCP module pair (CCP1/2), tethering active IL-33 within necrotic cells, preventing its release, and forestalling initiation of type 2 allergic responses. Thus, HpARI employs a novel molecular strategy to suppress type 2 immunity in both infection and allergy. Cell Press 2017-10-17 /pmc/articles/PMC5655542/ /pubmed/29045903 http://dx.doi.org/10.1016/j.immuni.2017.09.015 Text en © 2017 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Osbourn, Megan Soares, Dinesh C. Vacca, Francesco Cohen, E. Suzanne Scott, Ian C. Gregory, William F. Smyth, Danielle J. Toivakka, Matilda Kemter, Andrea M. le Bihan, Thierry Wear, Martin Hoving, Dennis Filbey, Kara J. Hewitson, James P. Henderson, Holly Gonzàlez-Cìscar, Andrea Errington, Claire Vermeren, Sonja Astier, Anne L. Wallace, William A. Schwarze, Jürgen Ivens, Alasdair C. Maizels, Rick M. McSorley, Henry J. HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33 |
title | HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33 |
title_full | HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33 |
title_fullStr | HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33 |
title_full_unstemmed | HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33 |
title_short | HpARI Protein Secreted by a Helminth Parasite Suppresses Interleukin-33 |
title_sort | hpari protein secreted by a helminth parasite suppresses interleukin-33 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5655542/ https://www.ncbi.nlm.nih.gov/pubmed/29045903 http://dx.doi.org/10.1016/j.immuni.2017.09.015 |
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