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新型 CS1 CAR-T 细胞与双特异性 CS1-BCMA CAR-T 细胞有效靶向多发性骨髓瘤

英文原题:Novel CS1 CAR-T Cells and Bispecific CS1-BCMA CAR-T Cells Effectively Target Multiple Myeloma.

查看英文原题

Novel CS1 CAR-T Cells and Bispecific CS1-BCMA CAR-T Cells Effectively Target Multiple Myeloma.

PubMed 2021/10/09(内容时间) Biomedicines Q2 · IF 4.5(JCR 2025)

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中文摘要

多发性骨髓瘤(MM)是一种由骨髓浆细胞异常增殖导致的血液系统癌症,这种致命疾病需要新型治疗方法。本研究旨在开发新型CS1 CAR-T 细胞和双特异性CS1-BCMA CAR-T 细胞,以特异性靶向多发性骨髓瘤。

我们生成了一种新型CS1(CD319、SLAM-7)抗体克隆7A8D5,可特异性识别CS1抗原,并用于构建CS1-CAR。CS1-CAR-T 细胞可特异性杀伤CHO-CS1靶细胞、分泌IFN-γ,并靶向多发性骨髓瘤细胞。

此外,双特异性CS1-BCMA-41BB-CD3 CAR-T 细胞能有效杀伤CHO-CS1和CHO-BCMA靶细胞、杀伤CS1/BCMA阳性多发性骨髓瘤细胞并分泌IFN-γ。

进一步地,CS1-CAR-T 细胞和双特异性CS1-BCMA CAR-T 细胞在体内均有效抑制MM1S多发性骨髓瘤肿瘤生长。这些数据首次证明,新型CS1及双特异性CS1-BCMA CAR-T 细胞能够有效靶向MM细胞,并为未来临床试验提供依据。

展开英文摘要原文

Multiple myeloma (MM) is a hematological cancer caused by abnormal proliferation of plasma cells in the bone marrow, and novel types of treatment are needed for this deadly disease. In this study, we aimed to develop novel CS1 CAR-T cells and bispecific CS1-BCMA CAR-T cells to specifically target multiple myeloma.

We generated a new CS1 (CD319, SLAM-7) antibody, clone (7A8D5), which specifically recognized the CS1 antigen, and we applied it for the generation of CS1-CAR. CS1-CAR-T cells caused specific killing of CHO-CS1 target cells with secretion of IFN-gamma and targeted multiple myeloma cells.

In addition, bispecific CS1-BCMA-41BB-CD3 CAR-T cells effectively killed CHO-CS1 and CHO-BCMA target cells, killed CS1/BCMA-positive multiple myeloma cells, and secreted IFN-gamma.

Moreover, CS1-CAR-T cells and bispecific CS1-BCMA CAR-T cells effectively blocked MM1S multiple myeloma tumor growth in vivo. These data for the first time demonstrate that novel CS1 and bispecific CS1-BCMA-CAR-T cells are effective in targeting MM cells and provide a basis for future clinical trials.

论文信息

作者
Golubovskaya V、Zhou H、Li F、Berahovich R、Sun J、Valentine M、Xu S、Harto H
单位
Promab Biotechnologies, 2600 Hilltop Drive, Richmond, CA 94806, USA.Italy
期刊
Biomedicines2021 Oct 9
原文标识
PubMed 34680541 · DOI 10.3390/biomedicines9101422