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将癌症免疫疗法转向新兴免疫检查点TIGIT:这会突破传统方法的局限吗?

Turning Cancer Immunotherapy to the Emerging Immune Checkpoint TIGIT: Will This Break Through the Limitations of the Legacy Approach?

作者信息

Cui Haozhe, Elkord Eyad

机构信息

Department of Biosciences and Bioinformatics, School of Science, Suzhou Municipal Key Lab in Biomedical Sciences and Translational Immunology, Xi'an Jiaotong-Liverpool University, Suzhou 215123, China.

College of Health Sciences, Abu Dhabi University, Abu Dhabi 59911, United Arab Emirates.

出版信息

Vaccines (Basel). 2024 Nov 22;12(12):1306. doi: 10.3390/vaccines12121306.

Abstract

The discovery of immune checkpoints (ICs) has pushed cancer treatment into the next era. As an emerging immune checkpoint, the TIGIT/CD155 axis inhibits the cytotoxicity of T and NK cells through multiple pathways. Immune checkpoint inhibitors (ICIs) targeting TIGIT are hopefully expected to address the issue of unresponsiveness to anti-PD-(L)1 monoclonal antibodies (mAbs) by combination therapy. This paper presents insights on the expression, structure and mechanism of action of TIGIT, as well as the principles and methods of designing mAbs targeting TIGIT and their clinical data. The advantages and disadvantages of targeting TIGIT using mAbs, bispecific and tri-specific antibodies (bsAbs and tsAbs), peptides, and compounds, in addition to potential combination therapies of anti-TIGIT with anti-PD-1 or cancer vaccines, are addressed. Finally, perspectives on current immunotherapies targeting TIGIT are discussed.

摘要

免疫检查点(ICs)的发现将癌症治疗推进到了一个新的时代。作为一种新兴的免疫检查点,TIGIT/CD155轴通过多种途径抑制T细胞和自然杀伤(NK)细胞的细胞毒性。有望通过联合治疗,使用靶向TIGIT的免疫检查点抑制剂(ICIs)来解决对抗程序性死亡蛋白-(配体)1(PD-(L)1)单克隆抗体(mAbs)无反应的问题。本文介绍了TIGIT的表达、结构和作用机制,以及靶向TIGIT的mAbs的设计原则和方法及其临床数据。文中还讨论了使用mAbs、双特异性和三特异性抗体(bsAbs和tsAbs)、肽和化合物靶向TIGIT的优缺点,以及抗TIGIT与抗PD-1或癌症疫苗联合治疗的潜在可能性。最后,对目前靶向TIGIT的免疫疗法进行了展望。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230b/11679306/b9f051e181c4/vaccines-12-01306-g001.jpg

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