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CD70 靶向同种异体 CAR-T 细胞治疗用于透明细胞肾细胞癌

英文原题:CD70-targeted allogeneic CAR T-cell therapy for clear cell renal cell carcinoma.

查看英文原题

CD70-targeted allogeneic CAR T-cell therapy for clear cell renal cell carcinoma.

PubMed 2025/08/18(内容时间) Expert Rev Anticancer Ther Q3 · IF 3(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

通用型 CAR-T 细胞的开发可能比自体 CAR-T 细胞治疗更经济、更易获得,并且能在更短时间内更易给药、机械故障更少。

中文摘要

引言:异体嵌合抗原受体(CAR)T 细胞疗法是透明细胞肾细胞癌(ccRCC)中有前景但研究不足的治疗方法,潜在疗效可能优于现有治疗。本综述比较了若干正在开展的 CAR-T 临床前和临床试验。综述范围:本文讨论 CAR-T 治疗 ccRCC 的发展,涵盖四个主题:(1)通过联合策略优化疗效;(2)从临床前开发到临床应用的转化路径;(3)安全性和毒性管理;(4)调节肿瘤微环境中的免疫应答。综述还指出克服现有限制并指导未来治疗的机会。研究者对过去 5 年 PubMed 和 Google Scholar 收录的研究进行结构化综述,汇总相关 ccRCC CAR-T 研究并归为四个主题,再交叉分析趋势、挑战和新出现的局限。专家观点:与自体 CAR-T 相比,通用型 CAR-T 可能成本更低、可及性更高、给药准备更快且机械故障更少。患者毒性、体内 CAR-T 细胞耗竭及免疫抑制性肿瘤微环境等问题仍待解决。

展开英文摘要原文

INTRODUCTION: Allogeneic chimeric antigen receptor (CAR) T-cell therapy is a promising yet underexplored treatment for clear cell renal cell carcinoma (ccRCC), potentially more effective than existing treatment options. This review compares several ongoing preclinical and clinical trials using CAR T-cell therapy.

AREAS COVERED: This review discusses the development of CAR T-cell therapy in ccRCC, covering four significant themes: (1) optimizing therapeutic efficacy through combination strategies, (2) the translation pathway from preclinical development to clinical application, (3) safety and toxicity management, and (4) immune response modulation in the tumor microenvironment.

Finally, this review highlights opportunities to overcome current limitations and guide future therapeutic approaches.

We conducted a structured review of existing research using the PubMed and Google Scholar databases from the past 5 years, compiled relevant studies on CAR T-cell therapies for ccRCC, and categorized them into four key themes, which were then cross-analyzed to identify trends, challenges, and emerging limitations.

EXPERT OPINION: Development of universal CAR T-cells may be more affordable, more accessible, and easier to administer in less time with fewer mechanical failures than autologous CAR T-cell therapy. Some challenges persist, including patient toxicities, depletion of CAR T-cells in vivo, and an immunosuppressive tumor microenvironment.

论文信息

作者
Bradley RL、Paul E、Singh S、Hutson TE
第一作者单位
School of Medicine, Texas Tech University Health Sciences Center, Lubbock, TX, USA.United States
通讯作者单位
University Medical Center Cancer Center.
文献类型
综述
期刊
Expert review of anticancer therapy2025 Nov
原文标识
PubMed 40803958 · DOI 10.1080/14737140.2025.2548489