| Literature DB >> 33767695 |
Deming Duan1,2, Keke Wang3,4, Cheng Wei3, Dudu Feng3, Yonghua Liu5, Qingyan He3, Xing Xu3, Chunling Wang3, Shuping Zhao3, Leili Lv5, Jing Long3, Danni Lin6, Ai Zhao4,7, Bingmu Fang5, Jinhong Jiang5, Shixing Tang1,2, Jimin Gao3,7.
Abstract
Chimeric antigen receptor (CAR) technology has revolutionized cancer treatment, particularly in malignant hematological tumors. Currently, the BCMA-targeted second-generation CAR-T cells have showed impressive efficacy in the treatment of refractory/relapsed multiple myeloma (R/R MM), but up to 50% relapse remains to be addressed urgently. Here we constructed the BCMA-targeted fourth-generation CAR-T cells expressing IL-7 and CCL19 (i.e., BCMA-7 × 19 CAR-T cells), and demonstrated that BCMA-7 × 19 CAR-T cells exhibited superior expansion, differentiation, migration and cytotoxicity. Furthermore, we have been carrying out the first-in-human clinical trial for therapy of R/R MM by use of BCMA-7 × 19 CAR-T cells (ClinicalTrials.gov Identifier: NCT03778346), which preliminarily showed promising safety and efficacy in first two enrolled patients. The two patients achieved a CR and VGPR with Grade 1 cytokine release syndrome only 1 month after one dose of CAR-T cell infusion, and the responses lasted more than 12-month. Taken together, BCMA-7 × 19 CAR-T cells were safe and effective against refractory/relapsed multiple myeloma and thus warranted further clinical study.Entities:
Keywords: BCMA; CAR-T; CCL19; IL-7; multiple myeloma
Year: 2021 PMID: 33767695 PMCID: PMC7985831 DOI: 10.3389/fimmu.2021.609421
Source DB: PubMed Journal: Front Immunol ISSN: 1664-3224 Impact factor: 7.561