Department of Hematology and Oncology, Shenzhen University General Hospital, Shenzhen Key Laboratory, Hematology Institution of Shenzhen University, Shenzhen Clinical Research Center for Hematologic Disease, International Cancer Center, Shenzhen University Health Science Center, Shenzhen University, Xueyuan AVE 1098, Shenzhen, 518000, China.
Shenzhen University-Haoshi Cell Therapy Institute, 155 Hong Tian Road, Bao An District, Shenzhen, 518125, China.
Blood Cancer J. 2024 Aug 7;14(1):130. doi: 10.1038/s41408-024-01105-8.
Non-Hodgkin lymphoma (NHL) is a common malignancy in the hematologic system, and traditional therapy has limited efficacy for people with recurrent/refractory NHL (R/R NHL), especially for patients with diffuse large B cell lymphoma (DLBCL). Chimeric antigen receptor (CAR) T-cell therapy is a novel and effective immunotherapy strategy for R/R hematopoietic malignancies, but relapses can occur due to the loss of CAR-T cells in vivo or the loss of antigen. One strategy to avoid antigen loss after CAR-T cell therapy is to target one more antigen simultaneously. Tandem CAR targeting CD19 and CD22 has demonstrated the reliability of tandem CAR-T cell therapy for R/R B-ALL. This study explores the therapeutic potential of tandem CD19/20 CAR-T in the treatment of R/R B cell NHL. The efficacy and safety of autologous CD19/20 CAR-T cells in eleven R/R B cell NHL adult patients were evaluated in an open-label, single-arm trial. Most patients achieved complete response, exhibiting the efficacy and safety of tandem CD19/20 CAR-T cells. The TCR repertoire diversity of CAR-T cells decreased after infusion. The expanded TCR clones in vivo were mainly derived from TCR clones that had increased expression of genes associated with immune-related signaling pathways from the infusion product (IP). The kinetics of CAR-T cells in vivo were linked to an increase in the expression of genes related to immune response and cytolysis/cytotoxicity.
非霍奇金淋巴瘤(NHL)是血液系统中的一种常见恶性肿瘤,传统疗法对复发/难治性 NHL(R/R NHL)患者,特别是弥漫性大 B 细胞淋巴瘤(DLBCL)患者疗效有限。嵌合抗原受体(CAR)T 细胞疗法是一种治疗 R/R 血液恶性肿瘤的新型有效免疫疗法策略,但由于体内 CAR-T 细胞的丢失或抗原的丢失,可能会发生复发。避免 CAR-T 细胞治疗后抗原丢失的一种策略是同时靶向一个以上的抗原。CD19 和 CD22 的串联 CAR 靶向已证明串联 CAR-T 细胞疗法治疗 R/R B-ALL 的可靠性。本研究探讨了串联 CD19/20 CAR-T 在治疗 R/R B 细胞 NHL 中的治疗潜力。在一项开放标签、单臂试验中,评估了十一例 R/R B 细胞 NHL 成年患者自体 CD19/20 CAR-T 细胞的疗效和安全性。大多数患者达到完全缓解,表明串联 CD19/20 CAR-T 细胞具有疗效和安全性。输注后 CAR-T 细胞的 TCR 谱多样性降低。体内扩增的 TCR 克隆主要来自输注产品(IP)中与免疫相关信号通路相关基因表达增加的 TCR 克隆。CAR-T 细胞在体内的动力学与与免疫反应和细胞溶解/细胞毒性相关的基因表达增加有关。