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高效生成过表达 CXCR4 的转基因增强型 CAR NK 细胞。

Highly Efficient Generation of Transgenically Augmented CAR NK Cells Overexpressing CXCR4.

机构信息

Faculty of Advanced Technologies in Medicine, Department of Molecular Medicine, Iran University of Medical Sciences, Tehran, Iran.

Molecular Biotechnology and Gene Therapy, Paul-Ehrlich-Institut, Langen, Germany.

出版信息

Front Immunol. 2020 Aug 28;11:2028. doi: 10.3389/fimmu.2020.02028. eCollection 2020.

Abstract

Natural killer (NK) cells are a noteworthy lymphocyte subset in cancer adoptive cell therapy. NK cells initiate innate immune responses against infections and malignancies with natural cytotoxicity, which is independent of foreign antigen recognition. Based on these substantive features, genetically modifying NK cells is among the prime goals in immunotherapy but is currently difficult to achieve. Recently, we reported a fully human CAR19 construct (huCAR19) with remarkable function in gene-modified T-cells. Here, we show efficient and stable gene delivery of huCAR19 to primary human NK cells using lentiviral vectors with transduction efficiencies comparable to those achieved with NK cell lines. These huCAR19 NK cells display specific and potent cytotoxic activity against target cells. To improve homing of NK cells to the bone marrow, we augmented huCAR19 NK cells with the human CXCR4 gene, resulting in transgenically augmented CAR NK cells (TRACKs). Compared to conventional CAR NK cells, TRACKs exhibit enhanced migration capacity in response to recombinant SDF-1 or bone marrow stromal cells while retaining functional and cytolytic activity against target cells. Based on these promising findings, TRACKs may become a novel candidate for immunotherapeutic strategies in clinical applications.

摘要

自然杀伤 (NK) 细胞是癌症过继细胞疗法中一种值得注意的淋巴细胞亚群。NK 细胞具有天然细胞毒性,可以启动针对感染和恶性肿瘤的固有免疫反应,而无需识别外来抗原。基于这些实质性特征,对 NK 细胞进行基因修饰是免疫治疗的首要目标之一,但目前难以实现。最近,我们报道了一种完全人源的 CAR19 构建体 (huCAR19),它在基因修饰的 T 细胞中具有显著的功能。在这里,我们使用慢病毒载体展示了 huCAR19 对原代人 NK 细胞的高效和稳定的基因传递,其转导效率可与 NK 细胞系相媲美。这些 huCAR19 NK 细胞对靶细胞表现出特异性和强大的细胞毒性活性。为了提高 NK 细胞向骨髓的归巢,我们用人类 CXCR4 基因增强了 huCAR19NK 细胞,从而产生了转基因增强型 CAR NK 细胞 (TRACKs)。与传统的 CAR NK 细胞相比,TRACKs 在响应重组 SDF-1 或骨髓基质细胞时表现出增强的迁移能力,同时保持对靶细胞的功能和细胞毒性活性。基于这些有希望的发现,TRACKs 可能成为临床应用中免疫治疗策略的一种新型候选物。

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