CD138-directed adoptive immunotherapy of chimeric antigen receptor (CAR)-modified T cells for multiple myeloma

Bo Guo , Meixia Chen , Qingwang Han , Fan Hui , Hanren Dai , Wenying Zhang , Yajing Zhang , Yao Wang , Hongli Zhu , Weidong Han
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引用次数: 139

Abstract

Adoptive immunotherapy with T cells expressing a tumor-associated chimeric antigen receptor (CAR) provides a promising approach for tumor therapy. We designed a clinical trial for multiple myeloma (MM) treatment with CAR-modified T cells recognizing CD138 (CART-138). Five patients diagnosed with chemotherapy-refractory MM were enrolled into this trial, although one later advanced to plasma cell leukemia. By intravenous infusions, these patients received CD3+ CART-138 cells in an escalating dose. No intolerable toxicity was observed during this process. CART-138 cells were expanded to a level 1000 times higher than the initial engraftment level and were maintained in the peripheral blood. In addition, increased CART-138 cells were also detected in the bone marrow. Four of the five patients had stable disease (SD) longer than three months, and one patient with advanced plasma cell leukemia had a reduction of the myeloma cells in her peripheral blood (from 10.5% to <3%). This study suggests that the treatment of CART-138 is safe, feasible, and tolerable and has potential antitumor activity in vivo, warranting further research in MM treatment using CART-138.

靶向cd138的嵌合抗原受体修饰T细胞过继免疫治疗多发性骨髓瘤
用表达肿瘤相关嵌合抗原受体(CAR)的T细胞进行过继免疫治疗为肿瘤治疗提供了一种很有前途的方法。我们设计了一项用car修饰的识别CD138的T细胞(CART-138)治疗多发性骨髓瘤(MM)的临床试验。5名诊断为化疗难治性MM的患者参加了这项试验,尽管其中一人后来进展为浆细胞白血病。通过静脉输注,这些患者接受了CD3+ CART-138细胞,剂量逐渐增加。在此过程中没有观察到无法忍受的毒性。CART-138细胞扩增到比初始植入水平高1000倍的水平,并维持在外周血中。此外,骨髓中也检测到CART-138细胞的增加。5例患者中有4例病情稳定(SD)超过3个月,1例晚期浆细胞白血病患者外周血中骨髓瘤细胞减少(从10.5%降至3%)。本研究提示CART-138治疗MM安全、可行、耐受,在体内具有潜在的抗肿瘤活性,值得进一步研究CART-138治疗MM。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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