CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Engineering Soluble Recombinant BCMA for Ide-Cel Labeling.
Engineering Soluble Recombinant BCMA for Ide-Cel Labeling.
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嵌合抗原受体(CAR)-T 细胞策略靶向多发性骨髓瘤(MM)患者恶性浆细胞表面表达的 B 细胞成熟抗原(BCMA)。Idecabtagene vicleucel(ide-cel)是一种抗 BCMA CAR-T 疗法,在治疗复发/难治性多发性骨髓瘤(R/RMM)中显示出有前景的结果。
值得注意的是,CAR-T 细胞扩增的程度与客观缓解率和完全缓解相关,表明监测 CAR-T 细胞对于预测这些患者的临床结局至关重要。尽管有几种工具可用于监测患者血液样本中的 CAR-T 细胞,但它们仍然昂贵,促使我们开发新的荧光和可溶性 BCMA 试剂用于 CAR-T 细胞标记。BCMA 是一种 III 型跨膜蛋白,我们发现由 BCMA 胞外域与绿色荧光蛋白(GFP)融合组成的重组构建体未能通过高尔基体转运,且未被分泌。加入干扰素-2 信号肽恢复了细胞内转运,并使可溶性 BCMA-GFP 和 BCMA-mCherry 融合蛋白能够高效分泌。这些试剂特异性标记了抗 BCMA CAR-T 细胞。
总体而言,我们的结果建立了一种经济有效的方法来生成可溶性 BCMA 探针,并为在转化环境中监测 CAR-T 细胞提供了可及的工具。
Chimeric antigen receptor (CAR)-T-based strategies target the B-cell maturation antigen (BCMA) expressed on the surface of malignant plasma cells in patients with multiple myeloma (MM). Idecabtagene vicleucel (ide-cel), an anti-BCMA CAR-T therapy, has shown promising results in the treatment of relapsed or refractory multiple myeloma (R/RMM).
Notably, the extent of CAR-T cell expansion correlates with objective response rates and complete responses, indicating that monitoring CAR-T cells is critical for predicting clinical outcomes in these patients. Although several tools are available to monitor CAR-T cells in patient blood samples, they remain costly, prompting us to develop novel fluorescent and soluble BCMA reagents for CAR-T cell labeling.
BCMA is a type III transmembrane protein, and we found that a recombinant construct consisting of the BCMA extracellular domain fused to green fluorescent protein (GFP) failed to traffic through the Golgi apparatus and was not secreted. Incorporation of the interferon- 2 signal peptide restored intracellular trafficking and enabled efficient secretion of soluble BCMA-GFP and BCMA-mCherry fusion proteins. These reagents specifically labeled anti-BCMA CAR-T cells.
Overall, our results establish a cost-effective method to generate soluble BCMA probes and provide accessible tools for monitoring CAR-T cells in translational settings.
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