Feldmann Anja, Arndt Claudia, Bergmann Ralf, Loff Simon, Cartellieri Marc, Bachmann Dominik, Aliperta Roberta, Hetzenecker Mirjam, Ludwig Florian, Albert Susann, Ziller-Walter Pauline, Kegler Alexandra, Koristka Stefanie, Gärtner Sebastian, Schmitz Marc, Ehninger Armin, Ehninger Gerhard, Pietzsch Jens, Steinbach Jörg, Bachmann Michael
Helmholtz-Zentrum Dresden-Rossendorf (HZDR), Institute of Radiopharmaceutical Cancer Research, Dresden, Germany.
UniversityCancerCenter (UCC) 'Carl Gustav Carus' TU Dresden, Tumor Immunology, Dresden, Germany.
Oncotarget. 2017 May 9;8(19):31368-31385. doi: 10.18632/oncotarget.15572.
New treatment options especially of solid tumors including for metastasized prostate cancer (PCa) are urgently needed. Recent treatments of leukemias with chimeric antigen receptors (CARs) underline their impressive therapeutic potential. However CARs currently applied in the clinics cannot be repeatedly turned on and off potentially leading to severe life threatening side effects. To overcome these problems, we recently described a modular CAR technology termed UniCAR: UniCAR T cells are inert but can be turned on by application of one or multiple target modules (TMs). Here we present preclinical data summarizing the retargeting of UniCAR T cells to PCa cells using TMs directed to prostate stem cell- (PSCA) or/and prostate specific membrane antigen (PSMA). In the presence of the respective TM(s), we see a highly efficient target-specific and target-dependent activation of UniCAR T cells, secretion of pro-inflammatory cytokines, and PCa cell lysis both in vitro and experimental mice.
迫切需要新的治疗方案,尤其是针对实体瘤,包括转移性前列腺癌(PCa)的治疗方案。最近用嵌合抗原受体(CAR)治疗白血病凸显了其令人印象深刻的治疗潜力。然而,目前临床上应用的CAR不能反复开启和关闭,这可能导致严重的危及生命的副作用。为了克服这些问题,我们最近描述了一种称为UniCAR的模块化CAR技术:UniCAR T细胞是惰性的,但可以通过应用一个或多个靶向模块(TM)来激活。在这里,我们展示了临床前数据,总结了使用针对前列腺干细胞抗原(PSCA)或/和前列腺特异性膜抗原(PSMA)的TM将UniCAR T细胞重新靶向至PCa细胞的情况。在存在相应TM的情况下,我们观察到UniCAR T细胞在体外和实验小鼠体内均出现高效的靶点特异性和靶点依赖性激活、促炎细胞因子的分泌以及PCa细胞裂解。