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면역미생물공생연구단
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Interleukin-2/antibody complex expanding Foxp3 + regulatory T cells exacerbates Th2-mediated allergic airway inflammation

DC Field Value Language
dc.contributor.authorSung-Wook Hong-
dc.contributor.authorEunju O-
dc.contributor.authorJun Young Lee-
dc.contributor.authorJaeu Yi-
dc.contributor.authorKyungjin Cho-
dc.contributor.authorJuhee Kim-
dc.contributor.authorDaeun Kim-
dc.contributor.authorCharles D. Surh-
dc.contributor.authorKwang Soon Kim-
dc.date.available2020-01-31T05:27:21Z-
dc.date.created2019-05-29-
dc.date.issued2019-04-
dc.identifier.issn1976-6696-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/6963-
dc.description.abstractFoxp3+ regulatory CD4+ T (Treg) cells play an essential role in preventing overt immune responses against self and innocuous foreign antigens. Selective expansion of endogenous Treg cells in response to the administration of interleukin (IL)-2/antibody complex, such as the IL-2/JES6-1 complex (IL-2C) in mice, is considered an attractive therapeutic approach to various immune disorders. Here, we investigated the therapeutic potential of IL-2C in allergic airway inflammation models. IL-2C treatment ameliorated Th17-mediated airway inflammation; however, unexpectedly, IL-2C treatment exacerbated Th2-mediated allergic airway inflammation by inducing the selective expansion of Th2 cells and type-2 innate lymphoid cells. We also found that IL-2 signaling is required for the expansion of Th2 cells in lymphoproliferative disease caused by Treg cell depletion. Our data suggest that IL-2C is selectively applicable to the treatment of allergic airway diseases depending on the characteristics of airway inflammation. [BMB Reports 2019; 52(4): 283-288]. ⓒ 2019 by the The Korean Society for Biochemistry and Molecular Biology-
dc.description.uri1-
dc.language영어-
dc.publisherKOREAN SOCIETY BIOCHEMISTRY & MOLECULAR BIOLOGY-
dc.subjectAirway inflammation, Foxp3+ regulatory T cell, IL-2/-
dc.subjectantibody complex, Th17, Th2-
dc.titleInterleukin-2/antibody complex expanding Foxp3 + regulatory T cells exacerbates Th2-mediated allergic airway inflammation-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000466556200008-
dc.identifier.scopusid2-s2.0-85065219033-
dc.identifier.rimsid68276-
dc.contributor.affiliatedAuthorSung-Wook Hong-
dc.contributor.affiliatedAuthorEunju O-
dc.contributor.affiliatedAuthorJun Young Lee-
dc.contributor.affiliatedAuthorJaeu Yi-
dc.contributor.affiliatedAuthorKyungjin Cho-
dc.contributor.affiliatedAuthorJuhee Kim-
dc.contributor.affiliatedAuthorDaeun Kim-
dc.contributor.affiliatedAuthorCharles D. Surh-
dc.contributor.affiliatedAuthorKwang Soon Kim-
dc.identifier.doi10.5483/bmbrep.2019.52.4.271-
dc.identifier.bibliographicCitationBMB REPORTS, v.52, no.4, pp.283 - 288-
dc.citation.titleBMB REPORTS-
dc.citation.volume52-
dc.citation.number4-
dc.citation.startPage283-
dc.citation.endPage288-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusIL-2-
dc.subject.keywordPlusDIFFERENTIATION-
dc.subject.keywordPlusACTIVATION-
dc.subject.keywordPlusRESOLUTION-
dc.subject.keywordPlusINDUCTION-
dc.subject.keywordPlusDISEASE-
dc.subject.keywordAuthorAirway inflammation-
dc.subject.keywordAuthorFoxp3(+) regulatory T cell-
dc.subject.keywordAuthorIL-2/antibody complex-
dc.subject.keywordAuthorTh17-
dc.subject.keywordAuthorTh2-
Appears in Collections:
Academy of Immunology and Microbiology(면역 미생물 공생 연구단) > 1. Journal Papers (저널논문)
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