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细胞因子诱导的杀伤细胞:异基因造血干细胞移植后过继性细胞免疫治疗的独特平台。

Cytokine-Induced Killer Cells: A Unique Platform for Adoptive Cell Immunotherapy after Allogeneic Hematopoietic Stem Cell Transplantation.

作者信息

Rettinger Eva

机构信息

Divsion of Stem Cell Transplantation, and Immunology, Department of Pediatrics, Goethe University Frankfurt, Frankfurt, Germany.

出版信息

Transfus Med Hemother. 2024 Sep 24;52(1):77-95. doi: 10.1159/000540964. eCollection 2025 Feb.

Abstract

BACKGROUND

Immunotherapies in general, and cellular immunotherapies, in particular are becoming increasingly integrated into current personalized cancer treatment, though still facing some obstacles in the allogeneic hematopoietic stem cell transplantation (HSCT) setting.

SUMMARY

The concept of isolating immune effector cells, expanding their numbers, enhancing their anticancer capabilities by modifying them without increasing their alloreactive potential is the mainstay of adoptive cellular immunotherapy after allogeneic HSCT. In this context, cytokine-induced killer (CIK) cells, a polyfunctional heterogenous population of conventional T cells, natural killer (NK) cells, and T-NK cells capable of using T cell and NK cell-like cytotoxicity mechanisms against a various cancers, showed minimal alloreactivity in pediatric and adult patients allografted for hematological malignancies. Furthermore, CIK cells have already shown compatibility with chemotherapy, different kinds of immune checkpoint inhibitors, epigenetic drugs, antibody-targeted therapies, and recently with chimeric antigen receptor-engineering techniques.

KEY MESSAGES

Hence, CIK cell therapy represents a unique platform for adoptive cell immunotherapies, guiding innovative treatment approaches from preclinical research to future clinical trials for cancer patients with yet unmet medical needs. In this context, the allogeneic HSCT setting provides an alternative source for safe and efficient adoptive allogeneic CIK cell strategies against a variety of cancers.

摘要

背景

一般而言,免疫疗法,尤其是细胞免疫疗法,正日益融入当前的个性化癌症治疗中,尽管在异基因造血干细胞移植(HSCT)环境中仍面临一些障碍。

总结

分离免疫效应细胞、扩增其数量、通过修饰增强其抗癌能力而不增加其同种异体反应潜能的概念是异基因HSCT后过继性细胞免疫疗法的核心。在这种情况下,细胞因子诱导的杀伤(CIK)细胞,一种由常规T细胞、自然杀伤(NK)细胞和T-NK细胞组成的多功能异质群体,能够利用T细胞和NK细胞样细胞毒性机制对抗多种癌症,在接受血液系统恶性肿瘤同种异体移植的儿科和成年患者中显示出最小的同种异体反应性。此外,CIK细胞已经显示出与化疗、不同种类的免疫检查点抑制剂、表观遗传药物、抗体靶向疗法兼容,最近还与嵌合抗原受体工程技术兼容。

关键信息

因此,CIK细胞疗法代表了一种独特的过继性细胞免疫疗法平台,指导着从临床前研究到针对尚未满足医疗需求的癌症患者的未来临床试验的创新治疗方法。在这种情况下,异基因HSCT环境为针对多种癌症的安全有效的过继性同种异体CIK细胞策略提供了替代来源。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ae7/11813276/2d2666b06f1d/tmh-2025-0052-0001-540964_F01.jpg

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