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  1. C100 医学部/医学系研究科
  2. C100a 雑誌掲載論文
  3. 学術雑誌

Roles of regulatory T cells in cancer immunity

http://hdl.handle.net/2237/25320
http://hdl.handle.net/2237/25320
43abe488-2a8b-473c-9344-978055ab1b1d
名前 / ファイル ライセンス アクション
s1-ln234847841682381206-1939656818Hwf-2035235115IdV16389160123484784PDF_HI0001.pdf s1-ln234847841682381206-1939656818Hwf-2035235115IdV16389160123484784PDF_HI0001.pdf ファイル公開:2017/08/01 (1.2 MB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-01-05
タイトル
タイトル Roles of regulatory T cells in cancer immunity
言語 en
著者 Takeuchi, Yoshiko

× Takeuchi, Yoshiko

WEKO 68545

en Takeuchi, Yoshiko

Search repository
Nishikawa, Hiroyoshi

× Nishikawa, Hiroyoshi

WEKO 68546

en Nishikawa, Hiroyoshi

Search repository
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
権利
言語 en
権利情報 This is a pre-copyedited, author-produced version of an article accepted for publication in [International Immunology] following peer review. The version of record [International Immunology. v.28, n.8, 2016, p.401-409] is available online at: http://doi.org/10.1093/intimm/dxw025.
キーワード
主題Scheme Other
主題 immune suppression
キーワード
主題Scheme Other
主題 immune checkpoint inhibitors
キーワード
主題Scheme Other
主題 Treg-targeted therapy
抄録
内容記述 CD4+ regulatory T cells (Tregs) expressing the transcription factor FoxP3 are highly immune suppressive and play central roles in the maintenance of self-tolerance and immune homeostasis, yet in malignant tumors they promote tumor progression by suppressing effective antitumor immunity. Indeed, higher infiltration by Tregs is observed in tumor tissues, and their depletion augments antitumor immune responses in animal models. Additionally, increased numbers of Tregs and, in particular, decreased ratios of CD8+ T cells to Tregs among tumor-infiltrating lymphocytes are correlated with poor prognosis in various types of human cancers. The recent success of cancer immunotherapy represented by immune checkpoint blockade has provided a new insight in cancer treatment, yet more than half of the treated patients did not experience clinical benefits. Identifying biomarkers that predict clinical responses and developing novel immunotherapies are therefore urgently required. Cancer patients whose tumors contain a large number of neoantigens stemming from gene mutations, which have not been previously recognized by the immune system, provoke strong antitumor T-cell responses associated with clinical responses following immune checkpoint blockade, depending on the resistance to Treg-mediated suppression. Thus, integration of a strategy restricting Treg-mediated immune suppression may expand the therapeutic spectrum of cancer immunotherapy towards patients with a lower number of neoantigens. In this review, we address the current understanding of Treg-mediated immune suppressive mechanisms in cancer, the involvement of Tregs in cancer immunotherapy, and strategies for effective and tolerable Treg-targeted therapy.
言語 en
内容記述タイプ Abstract
出版者
言語 en
出版者 Oxford University Press
言語
言語 eng
資源タイプ
資源タイプresource http://purl.org/coar/resource_type/c_6501
タイプ journal article
出版タイプ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1093/intimm/dxw025
ISSN
収録物識別子タイプ PISSN
収録物識別子 0953-8178
書誌情報 en : International Immunology

巻 28, 号 8, p. 401-409, 発行日 2016-08
著者版フラグ
値 author
URI
識別子 http://doi.org/10.1093/intimm/dxw025
識別子タイプ DOI
URI
識別子 http://hdl.handle.net/2237/25320
識別子タイプ HDL
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