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开发用于现货型癌症免疫治疗的同种异体 HSC 工程化 iNKT 细胞

英文原题:Development of allogeneic HSC-engineered iNKT cells for off-the-shelf cancer immunotherapy.

查看英文原题

Development of allogeneic HSC-engineered iNKT cells for off-the-shelf cancer immunotherapy.

PubMed 2021/11/16(内容时间) Cell Rep Med Q1 · IF 14(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。

中文摘要

基于细胞的免疫疗法已成为新一代的癌症药物,而能够大规模生产并随时分发给患者以治疗患者的“现货型”细胞产品是必要的。恒定自然杀伤T(iNKT)细胞是开发同种异体细胞疗法的理想细胞载体,因为它们是强大的免疫细胞,能够靶向癌症且无移植物抗宿主病(GvHD)风险。

然而,健康供者血液中内源性iNKT细胞数量极低。在此,通过结合造血干细胞(HSC)基因工程和体外分化,我们以高产率和纯度生成了人类同种异体HSC工程化iNKT(Allo HSC-iNKT)细胞;这些细胞与内源性iNKT细胞高度相似,通过多种机制有效靶向肿瘤细胞,并表现出高安全性和低免疫原性。这些细胞可进一步通过嵌合抗原受体(CAR)工程化改造以增强肿瘤靶向性,或/和通过基因编辑敲除表面人类白细胞抗原(HLA)分子以进一步降低免疫原性。

总体而言,这些临床前研究证明了Allo HSC-iNKT细胞产品的可行性和癌症治疗潜力,并为其转化和临床开发奠定了基础。

展开英文摘要原文

Cell-based immunotherapy has become the new-generation cancer medicine, and "off-the-shelf" cell products that can be manufactured at large scale and distributed readily to treat patients are necessary. Invariant natural killer T (iNKT) cells are ideal cell carriers for developing allogeneic cell therapy because they are powerful immune cells targeting cancers without graft-versus-host disease (GvHD) risk.

However, healthy donor blood contains extremely low numbers of endogenous iNKT cells.

Here, by combining hematopoietic stem cell (HSC) gene engineering and in vitro differentiation, we generate human allogeneic HSC-engineered iNKT ( Allo HSC-iNKT) cells at high yield and purity; these cells closely resemble endogenous iNKT cells, effectively target tumor cells using multiple mechanisms, and exhibit high safety and low immunogenicity.

These cells can be further engineered with chimeric antigen receptor (CAR) to enhance tumor targeting or/and gene edited to ablate surface human leukocyte antigen (HLA) molecules and further reduce immunogenicity. Collectively, these preclinical studies demonstrate the feasibility and cancer therapy potential of Allo HSC-iNKT cell products and lay a foundation for their translational and clinical development.

论文信息

作者
Li YR、Zhou Y、Kim YJ、Zhu Y、Ma F、Yu J、Wang YC、Chen X
单位
Department of Microbiology, Immunology & Molecular Genetics, University of California, Los Angeles, Los Angeles, CA 90095, USA.United States
文献类型
美国 NIH 资助研究 · 非美国政府资助研究
期刊
Cell reports. Medicine2021 Nov 16
原文标识
PubMed 34841295 · DOI 10.1016/j.xcrm.2021.100449