Promising New Anti-TIGIT Agents: Stealthy Allies in Cancer Immunotherapy

IF 3.1 3区 医学 Q2 MEDICINE, RESEARCH & EXPERIMENTAL
Gatadi Srikanth, Durga Prasad Beda, Ashish Ranjan Dwivedi, Nandan Kumar Duddukuri, Srinivas Nanduri, Jitendra Patel
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Abstract

TIGIT (T cell immunoreceptor with immunoglobulin and tyrosine-based inhibitory motif (ITIM) domain), Vstm3, and VSIG9, are newly recognized immunological checkpoints. They are prominently expressed on CD4+ and CD8+ T cells, tumor-infiltrating lymphocytes (TILs), natural killer (NK) cells, and regulatory T cells (Tregs). The TIGIT (TIGIT) protein is crucial for immune modulation since it diminishes NK cell populations and hinders T cell activity in cancer patients and experimental models. CD155, the principal ligand of TIGIT in humans, has been recognized as a pivotal target for immunotherapy owing to its interaction with TIGIT. CD155 is linked to the efficacy of anti-programmed cell death protein 1 (PD-1) therapy, even without TIGIT expression, underscoring its importance in immune checkpoint suppression. Anti-TIGIT medicines, either independently or in conjunction with anti-PD-1 treatments, have demonstrated potential in augmenting immune responses to malignancies. This review examines the structural and functional characteristics of the TIGIT protein, new developments in anti-TIGIT drugs, and their prospective use in cancer immunotherapy.

Abstract Image

有前景的新型抗tigit药物:癌症免疫治疗中的隐形盟友
TIGIT(带有免疫球蛋白和酪氨酸基抑制基序(ITIM)结构域的T细胞免疫受体)、Vstm3和VSIG9是新发现的免疫检查点。它们在CD4+和CD8+ T细胞、肿瘤浸润淋巴细胞(TILs)、自然杀伤细胞(NK)和调节性T细胞(Tregs)上显著表达。在癌症患者和实验模型中,TIGIT (TIGIT)蛋白对免疫调节至关重要,因为它减少NK细胞群并阻碍T细胞活性。CD155是人类TIGIT的主要配体,由于其与TIGIT的相互作用,已被认为是免疫治疗的关键靶点。CD155与抗程序性细胞死亡蛋白1 (PD-1)治疗的疗效相关,即使没有TIGIT表达,也强调了其在免疫检查点抑制中的重要性。抗tigit药物,无论是单独使用还是与抗pd -1治疗联合使用,已经证明在增强对恶性肿瘤的免疫应答方面具有潜力。本文综述了TIGIT蛋白的结构和功能特点、抗TIGIT药物的新进展及其在癌症免疫治疗中的应用前景。
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来源期刊
Cts-Clinical and Translational Science
Cts-Clinical and Translational Science 医学-医学:研究与实验
CiteScore
6.70
自引率
2.60%
发文量
234
审稿时长
6-12 weeks
期刊介绍: Clinical and Translational Science (CTS), an official journal of the American Society for Clinical Pharmacology and Therapeutics, highlights original translational medicine research that helps bridge laboratory discoveries with the diagnosis and treatment of human disease. Translational medicine is a multi-faceted discipline with a focus on translational therapeutics. In a broad sense, translational medicine bridges across the discovery, development, regulation, and utilization spectrum. Research may appear as Full Articles, Brief Reports, Commentaries, Phase Forwards (clinical trials), Reviews, or Tutorials. CTS also includes invited didactic content that covers the connections between clinical pharmacology and translational medicine. Best-in-class methodologies and best practices are also welcomed as Tutorials. These additional features provide context for research articles and facilitate understanding for a wide array of individuals interested in clinical and translational science. CTS welcomes high quality, scientifically sound, original manuscripts focused on clinical pharmacology and translational science, including animal, in vitro, in silico, and clinical studies supporting the breadth of drug discovery, development, regulation and clinical use of both traditional drugs and innovative modalities.
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