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  1. 原著論文

Activation-induced cytidine deaminase expression in CD4+ T cells is associated with a unique IL-10-producing subset that increases with age.

https://repo.qst.go.jp/records/46956
https://repo.qst.go.jp/records/46956
689a595e-c2d8-449b-b37f-eeb93c3ee4bd
Item type 学術雑誌論文 / Journal Article(1)
公開日 2014-11-19
タイトル
タイトル Activation-induced cytidine deaminase expression in CD4+ T cells is associated with a unique IL-10-producing subset that increases with age.
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 中島, 菜花子

× 中島, 菜花子

WEKO 468613

中島, 菜花子

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Hongyan, et.al Qin

× Hongyan, et.al Qin

WEKO 468614

Hongyan, et.al Qin

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中島 菜花子

× 中島 菜花子

WEKO 468615

en 中島 菜花子

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抄録
内容記述タイプ Abstract
内容記述 Activation-induced cytidine deaminase (AID), produced by the Aicda gene, is essential for the immunoglobulin gene (Ig) alterations that form immune memory. Using a Cre-mediated genetic system, we unexpectedly found CD4+ T cells that had expressed Aicda (exAID cells) as well as B cells. ExAID cells increased with age, reaching up to 25% of the CD4+ and B220+ cell populations. ExAID B cells remained IgM+, suggesting that class-switched memory B cells do not accumulate in the spleen. In T cells, AID was expressed in a subset that produced IFN-γ and IL-10 but little IL-4 or IL-17, and showed no evidence of genetic mutation. Interestingly, the endogenous Aicda expression in T cells was enhanced in the absence of B cells, indicating that the process is independent from the germinal center reaction. These results suggest that in addition to its roles in B cells, AID may have previously unappreciated roles in T-cell function or tumorigenesis.
書誌情報 PLoS ONE (Online only:URL:http://www.plosone.org)

巻 6, 号 12, p. e29141, 発行日 2011-12
ISSN
収録物識別子タイプ ISSN
収録物識別子 1932-6203
PubMed番号
識別子タイプ PMID
関連識別子 22216188
DOI
識別子タイプ DOI
関連識別子 10.1371/journal.pone.0029141
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