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nectin4 是一种新型的 TIGIT 配体,具有检查点抑制和肿瘤特异性。

Nectin4 is a novel TIGIT ligand which combines checkpoint inhibition and tumor specificity.

机构信息

The Concern Foundation Laboratories at the Lautenberg Center for Immunology and Cancer Research, Hebrew University Hadassah Medical School, Jerusalem, Israel.

Department of Histology and Embryology, Faculty of Medicine, University of Rijeka, Rijeka, Croatia.

出版信息

J Immunother Cancer. 2020 Jun;8(1). doi: 10.1136/jitc-2019-000266.

DOI:10.1136/jitc-2019-000266
PMID:32503945
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7279670/
Abstract

BACKGROUND

The use of checkpoint inhibitors has revolutionized cancer therapy. Unfortunately, these therapies often cause immune-related adverse effects, largely due to a lack of tumor specificity.

METHODS

We stained human natural killer cells using fusion proteins composed of the extracellular portion of various tumor markers fused to the Fc portion of human IgG1, and identified Nectin4 as a novel TIGIT ligand. Next, we generated a novel Nectin4 blocking antibody and demonstrated its efficacy as a checkpoint inhibitor in killing assays and in vivo.

RESULTS

We identify Nectin4 to be a novel ligand of TIGIT. We showed that, as opposed to all other known TIGIT ligands, which bind also additional receptors, Nectin4 interacts only with TIGIT. We show that the TIGIT-Nectin4 interaction inhibits natural killer cell activity, a critical part of the innate immune response. Finally, we developed blocking Nectin4 antibodies and demonstrated that they enhance tumor killing in vitro and in vivo.

CONCLUSION

We discovered that Nectin4 is a novel ligand for TIGIT and demonstrated that specific antibodies against it enhance tumor cell killing in vitro and in vivo. Since Nectin4 is expressed almost exclusively on tumor cells, our Nectin4-blocking antibodies represent a combination of cancer specificity and immune checkpoint activity, which may prove more effective and safe for cancer immunotherapy.

摘要

背景

检查点抑制剂的使用彻底改变了癌症治疗。不幸的是,这些疗法经常引起免疫相关的不良反应,这主要是由于缺乏肿瘤特异性。

方法

我们使用融合蛋白对人自然杀伤细胞进行染色,这些融合蛋白由各种肿瘤标志物的细胞外部分与人类 IgG1 的 Fc 部分融合而成,并鉴定出 Nectin4 是一种新型的 TIGIT 配体。接下来,我们生成了一种新型的 Nectin4 阻断抗体,并在杀伤实验和体内实验中证明了其作为检查点抑制剂的功效。

结果

我们确定 Nectin4 是 TIGIT 的一种新型配体。我们表明,与所有其他已知的 TIGIT 配体不同,它们还结合其他受体,而 Nectin4 仅与 TIGIT 相互作用。我们表明 TIGIT-Nectin4 相互作用抑制自然杀伤细胞的活性,这是先天免疫反应的关键部分。最后,我们开发了阻断 Nectin4 的抗体,并证明它们在体外和体内增强了肿瘤杀伤作用。

结论

我们发现 Nectin4 是 TIGIT 的一种新型配体,并证明针对它的特异性抗体增强了体外和体内的肿瘤细胞杀伤作用。由于 Nectin4 几乎仅在肿瘤细胞上表达,我们的 Nectin4 阻断抗体代表了癌症特异性和免疫检查点活性的结合,这可能在癌症免疫治疗中更有效和安全。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/d09faba5b989/jitc-2019-000266f07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/fa50d9c0b65e/jitc-2019-000266f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/67f428725b96/jitc-2019-000266f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/02ba64677de0/jitc-2019-000266f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/a824fea55f10/jitc-2019-000266f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/a3f5dba16608/jitc-2019-000266f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/b576fab0e5ed/jitc-2019-000266f06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/d09faba5b989/jitc-2019-000266f07.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/fa50d9c0b65e/jitc-2019-000266f01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/67f428725b96/jitc-2019-000266f02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/02ba64677de0/jitc-2019-000266f03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/a824fea55f10/jitc-2019-000266f04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/a3f5dba16608/jitc-2019-000266f05.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/b576fab0e5ed/jitc-2019-000266f06.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb75/7279670/d09faba5b989/jitc-2019-000266f07.jpg

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