CD8+ T cell-based immunotherapy: Promising frontier in human diseases

IF 5.6 2区 医学 Q1 PHARMACOLOGY & PHARMACY Biochemical pharmacology Pub Date : 2025-07-01 Epub Date: 2025-04-01 DOI:10.1016/j.bcp.2025.116909
Quynh Chau Ton Nu , Gitima Deka , Pil-Hoon Park
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Abstract

The abundant cell components of the adaptive immune system called T lymphocytes (T cells) play important roles in mediating immune responses to eliminate the invaders and create the memory of the germs to form a new immunity for the next encounter. Among them, cytotoxic T cells expressing cell-surface CD8 are the most critical effector cells that directly eradicate the target infected cells by recognizing antigens presented by major histocompatibility complex class I molecules to protect our body from pathological threats. In the continuous evolution of immunotherapy, various CD8+ T cell-based therapeutic strategies have been developed based on the role and molecular concept of CD8+ T cells. The emergence of such remarkable therapies provides promising hope for multiple human disease treatments such as autoimmunity, infectious disease, cancer, and other non-infectious diseases. In this review, we aim to discuss the current knowledge on the utilization of CD8+ T cell-based immunotherapy for the treatment of various diseases, the molecular basis involved, and its limitations. Additionally, we summarize the recent advances in the use of CD8+ T cell-based immunotherapy and provide a comprehensive overview of CD8+ T cells, including their structure, underlying mechanism of function, and markers associated with CD8+ T cell exhaustion. Building upon these foundations, we delineate the advancement of CD8+ T cell-based immunotherapies with fundamental operating principles followed by research studies, and challenges, as well as illustrate human diseases involved in this development.

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基于 CD8+ T 细胞的免疫疗法:在人类疾病领域大有可为的前沿。
适应性免疫系统中丰富的细胞成分T淋巴细胞(T细胞)在介导免疫反应中发挥重要作用,以消除入侵者,并产生细菌记忆,为下一次遭遇形成新的免疫系统。其中表达细胞表面CD8的细胞毒性T细胞是最关键的效应细胞,它通过识别主要组织相容性复合体I类分子呈递的抗原,直接消灭被感染的靶细胞,保护我们的身体免受病理威胁。随着免疫疗法的不断发展,基于CD8+ T细胞的作用和分子概念,各种基于CD8+ T细胞的治疗策略应运而生。这些显著疗法的出现为多种人类疾病的治疗提供了希望,如自身免疫、传染病、癌症和其他非传染性疾病。在这篇综述中,我们旨在讨论目前关于利用CD8+ T细胞免疫疗法治疗各种疾病的知识,所涉及的分子基础及其局限性。此外,我们总结了基于CD8+ T细胞的免疫治疗的最新进展,并提供了CD8+ T细胞的全面概述,包括它们的结构、潜在的功能机制和与CD8+ T细胞衰竭相关的标志物。在这些基础上,我们描述了基于CD8+ T细胞的免疫疗法的进展与基本的操作原则,随后的研究和挑战,并说明了涉及这一发展的人类疾病。
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来源期刊
Biochemical pharmacology
Biochemical pharmacology 医学-药学
CiteScore
10.30
自引率
1.70%
发文量
420
审稿时长
17 days
期刊介绍: Biochemical Pharmacology publishes original research findings, Commentaries and review articles related to the elucidation of cellular and tissue function(s) at the biochemical and molecular levels, the modification of cellular phenotype(s) by genetic, transcriptional/translational or drug/compound-induced modifications, as well as the pharmacodynamics and pharmacokinetics of xenobiotics and drugs, the latter including both small molecules and biologics. The journal''s target audience includes scientists engaged in the identification and study of the mechanisms of action of xenobiotics, biologics and drugs and in the drug discovery and development process. All areas of cellular biology and cellular, tissue/organ and whole animal pharmacology fall within the scope of the journal. Drug classes covered include anti-infectives, anti-inflammatory agents, chemotherapeutics, cardiovascular, endocrinological, immunological, metabolic, neurological and psychiatric drugs, as well as research on drug metabolism and kinetics. While medicinal chemistry is a topic of complimentary interest, manuscripts in this area must contain sufficient biological data to characterize pharmacologically the compounds reported. Submissions describing work focused predominately on chemical synthesis and molecular modeling will not be considered for review. While particular emphasis is placed on reporting the results of molecular and biochemical studies, research involving the use of tissue and animal models of human pathophysiology and toxicology is of interest to the extent that it helps define drug mechanisms of action, safety and efficacy.
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