CD38
单克隆抗体
抗体
细胞毒性T细胞
细胞毒性
免疫系统
癌症研究
程序性细胞死亡
蛋白酶体抑制剂
免疫学
生物
化学
多发性骨髓瘤
细胞凋亡
细胞生物学
体外
干细胞
生物化学
川地34
作者
Haotian Wu,Xiang‐Yu Zhao
摘要
CD38 is highly expressed on multiple myeloma (MM) cells and plays a role in regulating tumor generation and development.CD38 monoclonal antibodies (mAbs) have been used as an effective therapy for MM treatment by various mechanisms, including complement-dependent cytotoxic effects, antibodydependent cell-mediated cytotoxicity, antibody-dependent cellular phagocytosis, programmed cell death, enzymatic modulation, and immunomodulation.Although CD38 mAbs inhibit the proliferation and survival of MM cells, there are substantial side effects on antitumoral NK cells.The NK-mediated immune response needs to be further evaluated to minimize the adverse effects of NK cell loss.The killing effect of CD38 mAbs on CD38 high NK cells should be minimized and the potential combination of CD38 low/-NK cells and CD38 mAbs should be maximized to better benefit from their therapeutic efficacy against MM.CD38 mAb effects against MM can be maximized by combination therapies with immunomodulatory imide drugs (IMiDs), proteasome inhibitors (PIs), anti-programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) antibodies, or cellular therapies for the treatment of MM, especially in patients with relapsed or refractory MM (R/R MM) and drug-resistant MM.
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