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CD39 的调控与 T 细胞功能

CD39 Regulation and Functions in T Cells.

机构信息

Department of Immunology, PSL Research University, INSERM U932, Institut Curie, 26, rue d'Ulm, 75005 Paris, France.

Department of Internal Clinical Sciences, Anaesthesiology and Cardiovascular Sciences, Sapienza Università di Roma, 00161 Rome, Italy.

出版信息

Int J Mol Sci. 2021 Jul 28;22(15):8068. doi: 10.3390/ijms22158068.


DOI:10.3390/ijms22158068
PMID:34360833
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8348030/
Abstract

CD39 is an enzyme which is responsible, together with CD73, for a cascade converting adenosine triphosphate into adenosine diphosphate and cyclic adenosine monophosphate, ultimately leading to the release of an immunosuppressive form of adenosine in the tumor microenvironment. Here, we first review the environmental and genetic factors shaping CD39 expression. Second, we report CD39 functions in the T cell compartment, highlighting its role in regulatory T cells, conventional CD4 T cells and CD8 T cells. Finally, we compile a list of studies, from preclinical models to clinical trials, which have made essential contributions to the discovery of novel combinatorial approaches in the treatment of cancer.

摘要

CD39 是一种酶,与 CD73 一起负责一系列反应,将三磷酸腺苷转化为二磷酸腺苷和环磷酸腺苷,最终导致肿瘤微环境中免疫抑制形式的腺苷释放。在这里,我们首先回顾了影响 CD39 表达的环境和遗传因素。其次,我们报告了 CD39 在 T 细胞区室中的功能,重点介绍了其在调节性 T 细胞、常规 CD4 T 细胞和 CD8 T 细胞中的作用。最后,我们整理了一系列研究,从临床前模型到临床试验,这些研究对发现癌症治疗的新组合方法做出了重要贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63c9/8348030/0e3536379042/ijms-22-08068-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63c9/8348030/0e3536379042/ijms-22-08068-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/63c9/8348030/0e3536379042/ijms-22-08068-g001.jpg

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[1]
CD39 Regulation and Functions in T Cells.

Int J Mol Sci. 2021-7-28

[2]
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[3]
Adenosine and the adenosine A2A receptor agonist, CGS21680, upregulate CD39 and CD73 expression through E2F-1 and CREB in regulatory T cells isolated from septic mice.

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[4]
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[5]
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PLoS One. 2018-5-9

[6]
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[7]
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[8]
Role of the CD39/CD73 Purinergic Pathway in Modulating Arterial Thrombosis in Mice.

Arterioscler Thromb Vasc Biol. 2016-9

[9]
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FASEB J. 2009-2

[10]
Synergy between the ectoenzymes CD39 and CD73 contributes to adenosinergic immunosuppression in human malignant gliomas.

Neuro Oncol. 2013-6-4

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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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[10]
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本文引用的文献

[1]
Implication of CD69 CD103 tissue-resident-like CD8 T cells as a potential immunotherapeutic target for cholangiocarcinoma.

Liver Int. 2021-4

[2]
Detection of CD39 and a Highly Glycosylated Isoform of Soluble CD73 in the Plasma of Patients with Cervical Cancer: Correlation with Disease Progression.

Mediators Inflamm. 2020

[3]
Enhanced expression of CD39 and CD73 on T cells in the regulation of anti-tumor immune responses.

Oncoimmunology. 2020-4-9

[4]
High Expression of CD39 is Associated with Poor Prognosis and Immune Infiltrates in Clear Cell Renal Cell Carcinoma.

Onco Targets Ther. 2020-10-14

[5]
Inhibition of the Adenosine Pathway to Potentiate Cancer Immunotherapy: Potential for Combinatorial Approaches.

Annu Rev Med. 2021-1-27

[6]
CD39 Identifies the CD4 Tumor-Specific T-cell Population in Human Cancer.

Cancer Immunol Res. 2020-10

[7]
Targeting CD39 in cancer.

Nat Rev Immunol. 2020-12

[8]
CD73 acts as a prognostic biomarker and promotes progression and immune escape in pancreatic cancer.

J Cell Mol Med. 2020-8

[9]
IL-6-induced CD39 expression on tumor-infiltrating NK cells predicts poor prognosis in esophageal squamous cell carcinoma.

Cancer Immunol Immunother. 2020-6-10

[10]
Genetically driven CD39 expression shapes human tumor-infiltrating CD8 T-cell functions.

Int J Cancer. 2020-11-1

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