Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/110992
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Type: Journal article
Title: Interleukin-5 mediates parasite-induced protection against experimental autoimmune encephalomyelitis: association with induction of antigen-specific CD4⁺ CD25⁺ T regulatory cells
Other Titles: Interleukin-5 mediates parasite-induced protection against experimental autoimmune encephalomyelitis: association with induction of antigen-specific CD4(+) CD25(+) T regulatory cells
Author: Tran, G.
Wilcox, P.
Dent, L.
Robinson, C.
Carter, N.
Verma, N.
Hall, B.
Hodgkinson, S.
Citation: Frontiers in Immunology, 2017; 8(NOV):1453-1-1453-13
Publisher: Frontiers Media
Issue Date: 2017
ISSN: 1664-3224
1664-3224
Statement of
Responsibility: 
Giang T. Tran, Paul L. Wilcox, Lindsay A. Dent, Catherine M. Robinson, Nicole Carter, Nirupama D. Verma, Bruce M. Hall and Suzanne J. Hodgkinson
Abstract: Objective: To examine if the protective effect of parasite infection on experimental autoimmune encephalomyelitis (EAE) was due to interleukin (IL)-5, a cytokine produced by a type-2 response that induces eosinophilia. We hypothesize that, in parasite infections, IL-5 also promotes expansion of antigen-specific T regulatory cells that control autoimmunity. Methods: Nippostrongylus brasiliensis larvae were used to infect Lewis rats prior to induction of EAE by myelin basic protein. Animals were sham treated, or given blocking monoclonal antibodies to interleukin 4 or 5 or to deplete CD25+ T cells. Reactivity of CD4+CD25+ T regulatory cells from these animals was examined. Results: Parasite-infected hosts had reduced severity and length of EAE. The beneficial effect of parasitic infection was abolished with an anti-IL-5 or an anti-CD25 monoclonal antibody (mAb), but not anti-IL-4 mAb. Parasite-infected animals with EAE developed antigen-specific CD4+CD25+ T regulatory cells earlier than EAE controls and these expressed more Il5ra than controls. Treatment with IL-5 also reduced the severity of EAE and induced Il5ra expressing CD4+CD25+ T regulatory cells. Interpretation: The results of this study suggested that IL-5 produced by the type-2 inflammatory response to parasite infection promoted induction of autoantigen-specific CD25+Il5ra+ T regulatory cells that reduced the severity of autoimmunity. Such a mechanism may explain the protective effect of parasite infection in patients with multiple sclerosis where eosinophilia is induced by IL-5, produced by the immune response to parasites.
Keywords: Treg cells; autoimmunity; experimental autoimmune encephalomyelitis; interleukin-5; parasite infection
Rights: © 2017 Tran, Wilcox, Dent, Robinson, Carter, Verma, Hall and Hodgkinson. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
RMID: 0030077829
DOI: 10.3389/fimmu.2017.01453
Grant ID: http://purl.org/au-research/grants/nhmrc/1047069
Appears in Collections:Molecular and Biomedical Science publications

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