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:Developmental Therapeutics in Metastatic Prostate Cancer: New Targets and New Strategies.
Developmental Therapeutics in Metastatic Prostate Cancer: New Targets and New Strategies.
转移性前列腺癌新疗法的开发存在未满足的需求。
转移性前列腺癌新疗法的开发存在未满足的需求。随着靶向放射性配体疗法、双特异性T细胞衔接器、抗体药物偶联物和CAR-T 细胞(CAR T)疗法的发展,肿瘤相关细胞表面抗原已成为转移性前列腺癌的新治疗靶点。本文综述了针对前列腺特异性膜抗原(PSMA)、前列腺六跨膜上皮抗原1(STEAP1)、激肽释放酶相关肽酶2(KLK2)、前列腺干细胞抗原(PSCA)和δ样蛋白3(DLL3)在转移性前列腺癌中正在进行和已完成的临床试验。讨论了序贯或联合治疗的策略。
There is an unmet need to develop new treatments for metastatic prostate cancer. With the development of targeted radioligand therapies, bispecific T cell engagers, antibody-drug conjugates and chimeric antigen receptor T cell (CAR T) therapies, tumor-associated cell surface antigens have emerged as new therapeutic targets in metastatic prostate cancer. Ongoing and completed clinical trials targeting prostate-specific membrane antigen (PSMA), six transmembrane epithelial antigens of the prostate 1 (STEAP1), kallikrein-related peptidase 2 (KLK2), prostate stem cell antigen (PSCA), and delta-like protein 3 (DLL3) in metastatic prostate cancer were reviewed. Strategies for sequential or combinational therapy were discussed.
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