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PD-L1 在缺血再灌注损伤中的免疫调节中的分歧作用。

Divergent roles of PD-L1 in immune regulation during ischemia-reperfusion injury.

机构信息

Department of Neurology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.

出版信息

Front Immunol. 2022 Nov 21;13:1021452. doi: 10.3389/fimmu.2022.1021452. eCollection 2022.

DOI:10.3389/fimmu.2022.1021452
PMID:36479124
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9720307/
Abstract

Ischemia-reperfusion (I/R) injury is a type of pathological injury that commonly arises in various diseases. Various forms of immune response are involved in the process of I/R injury. As a member of the B7 costimulatory molecule family, programmed death 1-ligand 1 (PD-L1) is an important target for immune regulation. Therefore, PD-L1 may be implicated in the regulation of I/R injury. This review briefly describes the immune response during I/R injury and how PD-L1 is involved in its regulation by focusing on findings from various I/R models. Despite the limited number of studies in this field of research, PD-L1 has shown sufficient potential as a clinical therapeutic target.

摘要

缺血再灌注(I/R)损伤是一种常见于各种疾病的病理损伤。各种形式的免疫反应都参与了 I/R 损伤的过程。程序性死亡配体 1(PD-L1)作为 B7 共刺激分子家族的一员,是免疫调节的重要靶点。因此,PD-L1 可能参与了 I/R 损伤的调节。本综述简要描述了 I/R 损伤过程中的免疫反应,以及 PD-L1 如何通过聚焦于各种 I/R 模型中的发现来参与其调节。尽管该研究领域的研究数量有限,但 PD-L1 已显示出作为临床治疗靶点的巨大潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5364/9720307/cda094920b87/fimmu-13-1021452-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5364/9720307/754adec7349d/fimmu-13-1021452-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5364/9720307/027fafa619dc/fimmu-13-1021452-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5364/9720307/cda094920b87/fimmu-13-1021452-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5364/9720307/754adec7349d/fimmu-13-1021452-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5364/9720307/027fafa619dc/fimmu-13-1021452-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5364/9720307/cda094920b87/fimmu-13-1021452-g003.jpg

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本文引用的文献

1
Compartmentalization of Intrarenal Programmed Cell Death Protein 1-Ligand 1 and Its Receptor in Kidney Injury Related to Immune Checkpoint Inhibitor Nephrotoxicity.肾内程序性细胞死亡蛋白1-配体1及其受体在与免疫检查点抑制剂肾毒性相关的肾损伤中的区室化
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2
Exosomal PD-L1 induces osteogenic differentiation and promotes fracture healing by acting as an immunosuppressant.外泌体程序性死亡配体1通过作为一种免疫抑制剂诱导成骨分化并促进骨折愈合。
Bioact Mater. 2021 Nov 3;13:300-311. doi: 10.1016/j.bioactmat.2021.10.042. eCollection 2022 Jul.
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Elevated Plasma Soluble PD-L1 Levels in Out-of-Hospital Cardiac Arrest Patients.
院外心脏骤停患者血浆可溶性程序性死亡配体1水平升高
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Overexpression of genes involved in lymphocyte activation and regulation are associated with reduced CRM-derived cardiac remodelling after STEMI.淋巴细胞激活和调节相关基因的过表达与 STEMI 后 CRM 衍生的心脏重构减少有关。
Int Immunopharmacol. 2021 Jun;95:107490. doi: 10.1016/j.intimp.2021.107490. Epub 2021 Mar 4.
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Variable Expression of Programmed Cell Death Protein 1-Ligand 1 in Kidneys Independent of Immune Checkpoint Inhibition.程序性细胞死亡蛋白 1 配体 1 在肾脏中的可变表达与免疫检查点抑制无关。
Front Immunol. 2021 Jan 21;11:624547. doi: 10.3389/fimmu.2020.624547. eCollection 2020.
6
Dual and Opposite Costimulatory Targeting with a Novel Human Fusion Recombinant Protein Effectively Prevents Renal Warm Ischemia Reperfusion Injury and Allograft Rejection in Murine Models.新型人融合重组蛋白的双重和相反共刺激靶向治疗可有效预防小鼠肾热缺血再灌注损伤和移植物排斥反应。
Int J Mol Sci. 2021 Jan 26;22(3):1216. doi: 10.3390/ijms22031216.
7
Soluble PD-L1 improved direct ARDS by reducing monocyte-derived macrophages.可溶性 PD-L1 通过减少单核细胞衍生的巨噬细胞改善直接 ARDS。
Cell Death Dis. 2020 Oct 30;11(10):934. doi: 10.1038/s41419-020-03139-9.
8
Avelumab Maintenance Therapy for Advanced or Metastatic Urothelial Carcinoma.阿维鲁单抗维持治疗晚期或转移性尿路上皮癌。
N Engl J Med. 2020 Sep 24;383(13):1218-1230. doi: 10.1056/NEJMoa2002788. Epub 2020 Sep 18.
9
Stroke.中风。
Lancet. 2020 Jul 11;396(10244):129-142. doi: 10.1016/S0140-6736(20)31179-X.
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