Division of Hematology and Oncology, Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Genepeutic Bio, Co. Ltd., Bangkok, Thailand.
PLoS One. 2023 Feb 13;18(2):e0281735. doi: 10.1371/journal.pone.0281735. eCollection 2023.
T cells genetically engineered to express a chimeric antigen receptor (CAR) specifically binding to a CD19 antigen has become the frontline of hematological malignancies immunotherapy. Their remarkable antitumor effect has exerted complete remission in treating B-cell malignancies. Although successful patient treatment has been shown, improvement to the structure of CAR to enhance its safety and efficacy profile is warranted. Transduction with a lentiviral vector (LVV) leading to the expression of CARs is also a critical step in redirecting T cells to target specific tumor antigens. To improve the efficacy of CD19 CARs in this study, the transduction ability of second and third generations LVV were compared. Ex vivo expansion of CD19 CARs T cells from healthy donors' peripheral blood mononuclear cells was performed after transduction of T cells with second and third generations LVV. Transduction efficacy of transduced T cells was determined to show a higher percentage in the third generations LVV transduced cells, with no changes in viability and identity of cells characterized by immunophenotyping. Testing the cytotoxic capacity of third generations LVV-transduced T cells against target cells showed higher reactivity against control cells. Cytokine expression was detected on the CD19 CARs T cells, suggesting that these cells limit in vitro growth of B-cell leukemia via secretion of the pro-inflammatory cytokine IFN γ. To investigate whether the third generation LVV transduced T cells can limit CD19 lymphoma growth in vivo, an analysis of tumor burden in a mouse model assessed by bioluminescence imaging was performed. We found that, in the presence of CD19 CARs T cells, the level of tumor burden was markedly reduced. In addition, an increase in the length of survival in mice receiving CAR-CD19 T cells was also observed. This suggests that transduction with third generations LVV generate a functional CAR-CD19 T cells, which may provide a safer and effective therapy for B-cell malignancies.
经基因工程改造表达嵌合抗原受体(CAR)的 T 细胞,该受体特异性结合 CD19 抗原,已成为血液恶性肿瘤免疫治疗的前沿。它们对肿瘤的显著抗肿瘤作用已在治疗 B 细胞恶性肿瘤中实现完全缓解。尽管已经显示出成功的患者治疗效果,但改进 CAR 的结构以增强其安全性和疗效谱是必要的。用慢病毒载体(LVV)转导以表达 CAR 也是将 T 细胞重定向至靶向特定肿瘤抗原的关键步骤。为了提高 CD19 CAR 在本研究中的疗效,比较了第二代和第三代 LVV 的转导能力。从健康供体外周血单核细胞中扩增 CD19 CAR T 细胞后,用第二代和第三代 LVV 转导 T 细胞。通过测定转导细胞的转导效率,表明第三代 LVV 转导细胞的转导效率更高,细胞活力和表型特征没有变化。测试第三代 LVV 转导的 T 细胞对靶细胞的细胞毒性能力表明,对对照细胞的反应性更高。检测到 CD19 CAR T 细胞的细胞因子表达,表明这些细胞通过分泌促炎细胞因子 IFN γ来限制 B 细胞白血病的体外生长。为了研究第三代 LVV 转导的 T 细胞是否能在体内限制 CD19 淋巴瘤的生长,通过生物发光成像分析评估了小鼠模型中的肿瘤负担。我们发现,在存在 CD19 CAR T 细胞的情况下,肿瘤负担水平显著降低。此外,还观察到接受 CAR-CD19 T 细胞的小鼠的生存时间延长。这表明第三代 LVV 的转导产生了功能性 CAR-CD19 T 细胞,这可能为 B 细胞恶性肿瘤提供更安全有效的治疗方法。