决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:Idecabtagene vicleucel for relapsed/refractory multiple myeloma: a review of recent advances.
Idecabtagene vicleucel for relapsed/refractory multiple myeloma: a review of recent advances.
过去20年间,治疗多发性骨髓瘤(MM)的新类别药物,如蛋白酶体抑制剂、免疫调节剂和抗CD38单克隆抗体,结合自体干细胞移植,已将MM患者的5年生存率大约提高了一倍。
过去20年中,蛋白酶体抑制剂、免疫调节剂和抗CD38单克隆抗体等新型多发性骨髓瘤(MM)药物,加上自体干细胞移植,使MM患者5年生存率大约翻倍。然而,患者最终仍会复发和/或对药物及治疗产生耐药。近期出现的抗B细胞成熟抗原(BCMA)疗法,尤其是靶向BCMA的CAR-T 细胞免疫疗法,在MM治疗中前景广阔。本文详细回顾idecabtagene vicleucel(ide-cel,bb-2121)的进展。ide-cel是首个靶向BCMA的CAR-T疗法,于2021年获美国食品药品监督管理局批准用于复发或难治性MM,本文回顾其临床前研究及I、II期临床试验。本文还指出,尽管ide-cel临床疗效令人瞩目且毒性相对较低,未来仍有许多挑战和未解决问题。
The introduction of new classes of drugs for the treatment of multiple myeloma (MM) in the past 2 decades, such as proteasome inhibitors, immunomodulators and anti-CD38 monoclonal antibodies, coupled with autologous stem cell transplantation, has approximately doubled the 5-year survival rate of MM patients. However, the patients eventually relapse and/or become resistant to the drugs and treatment. The recent emergence of anti-B-cell maturation antigen (BCMA) therapies, especially chimeric antigen receptor T-cell (CAR-T) immunotherapy targeting BCMA, holds great prospect in MM treatment. In this article, we review in detail the advances of idecabtagene vicleucel (ide-cel, bb-2121), the first CAR-T therapy targeting BCMA for treating relapse or refractory MM approved by the U.S. Food and Drug Administration (FDA) in 2021, including the preclinical study and phase I and II clinical trials. Also, it is predicted in this review that despite its amazing clinical efficacy and relatively lower toxicity, a lot of challenges and unsolved problems for ide-cel therapy remain in the way ahead.
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