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  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 1. 査読済論文(医学・保健)

Naturally-occurring regulatory T cells are increased in inflamed portal tracts with cholangiopathy in primary biliary cirrhosis1102-1107

http://hdl.handle.net/2297/19776
http://hdl.handle.net/2297/19776
b4c35f0b-8d76-4f37-8582-46b5723f4986
名前 / ファイル ライセンス アクション
ME-PR-NAKANUMA-Y-1102.pdf ME-PR-NAKANUMA-Y-1102.pdf (894.2 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-03
タイトル
タイトル Naturally-occurring regulatory T cells are increased in inflamed portal tracts with cholangiopathy in primary biliary cirrhosis1102-1107
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
著者 Sasaki, Motoko

× Sasaki, Motoko

WEKO 129
e-Rad 70225895
金沢大学研究者情報 70225895
研究者番号 70225895

Sasaki, Motoko

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Ikeda, Hiroko

× Ikeda, Hiroko

WEKO 642
e-Rad 10447675
金沢大学研究者情報 10447675
研究者番号 10447675

Ikeda, Hiroko

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Sawada, Seiko

× Sawada, Seiko

WEKO 26057

Sawada, Seiko

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Sato, Yasunori

× Sato, Yasunori

WEKO 249
e-Rad 30324073
金沢大学研究者情報 30324073
研究者番号 30324073

Sato, Yasunori

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Nakanuma, Yasuni

× Nakanuma, Yasuni

WEKO 92
e-Rad 10115256
研究者番号 10115256

Nakanuma, Yasuni

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提供者所属
内容記述タイプ Other
内容記述 金沢大学医薬保健研究域医学系
書誌情報 Journal of Clinical Pathology

巻 60, 号 10, p. 1102-1107, 発行日 2007-10-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0021-9746
NCID
収録物識別子タイプ NCID
収録物識別子 AA00695564
DOI
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 10.1136/jcp.2006.044776
出版者
出版者 BMJ Publishing Group
抄録
内容記述タイプ Abstract
内容記述 Background: Primary biliary cirrhosis (PBC) is an autoimmune liver disease targeting the intrahepatic small bile ducts showing chronic non-suppurative destructive cholangitis (CNSDC). Recent studies suggest that naturally-occurring CD4+CD25high regulatory T cells (Tregs) expressing Forkhead box P3 (Foxp3) play an active role in immunological self-tolerance. Aims: To investigate whether Foxp3+Tregs are involved in the pathogenesis of PBC. Methods: Foxp3+Tregs was detected immunohistochemically in livers from patients with PBC (n = 27), chronic viral hepatitis (CVH) (n = 15), and normal subjects (n = 10). The distribution of Tregs in portal tracts was semi-quantitatively evaluated in each groups. Levels of Foxp3, IL-10, TGFβ, IFNγ and TNFα mRNA was evaluated in PBC (n= 15) and control livers (n = 21) using semi-quantitative reverse transcriptase-PCR. Results: In PBC and CVH livers, the amounts of infiltrating Foxp3+Tregs in portal tracts were in parallel with the degree of portal inflammation irrespective of disease. The infiltration of Foxp3+Tregs into portal tracts with CNSDC in PBC was foremost in comparison with inflamed portal tracts in CVH or those without CNSDC in PBC (p<0.05). Focally, Tregs infiltrated into the biliary epithelial layer at the site of CNSDC. The level of Foxp3, IL-10 and TGFβ mRNA expression was high in PBC compared with normal livers (p<0.05). IFNγ and TNFα mRNA was high in early PBC and CVH livers. Conclusion: Results of this evaluation of Foxp3+Tregs do not suggest that the reduced regulatory function accounts for the development of CNSDC in PBC.
権利
権利情報 Copyright © 2007 by the BMJ Publishing Group Ltd & Association of Clinical Pathologists
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
関連URI
識別子タイプ URI
関連識別子 http://gut.bmj.com/cgi/content/extract/56/10/1471
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