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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cell Press 2017
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.
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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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