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:Targeting advanced prostate cancer with STEAP1 chimeric antigen receptor T cell and tumor-localized IL-12 immunotherapy.
前列腺六跨膜上皮抗原 1(STEAP1)是前列腺癌治疗靶向的细胞表面抗原。
前列腺六跨膜上皮抗原1(STEAP1)是前列腺癌表面治疗靶点。本研究发现,在致死性转移性前列腺癌中,STEAP1相较前列腺特异性膜抗原(PSMA)广泛表达,并开发了靶向STEAP1的CAR-T。STEAP1 CAR-T在低抗原密度下仍能识别,在多种转移性前列腺癌模型中有抗肿瘤活性,且在人STEAP1敲入小鼠中显示安全性。STEAP1抗原逃逸是反复出现的耐药机制,并与肿瘤抗原加工和呈递下降有关。将肿瘤局部白介素12(IL-12)治疗(胶原结合结构域CBD-IL-12融合蛋白)与STEAP1 CAR-T联合,可重塑前列腺癌免疫“冷”微环境,并通过动员宿主免疫和表位扩展对抗STEAP1抗原逃逸,从而增强抗肿瘤疗效。
Six transmembrane epithelial antigen of the prostate 1 (STEAP1) is a cell surface antigen for therapeutic targeting in prostate cancer. Here, we report broad expression of STEAP1 relative to prostate-specific membrane antigen (PSMA) in lethal metastatic prostate cancers and the development of a STEAP1-directed chimeric antigen receptor (CAR) T cell therapy. STEAP1 CAR T cells demonstrate reactivity in low antigen density, antitumor activity across metastatic prostate cancer models, and safety in a human STEAP1 knock-in mouse model. STEAP1 antigen escape is a recurrent mechanism of treatment resistance and is associated with diminished tumor antigen processing and presentation. The application of tumor-localized interleukin-12 (IL-12) therapy in the form of a collagen binding domain (CBD)-IL-12 fusion protein combined with STEAP1 CAR T cell therapy enhances antitumor efficacy by remodeling the immunologically cold tumor microenvironment of prostate cancer and combating STEAP1 antigen escape through the engagement of host immunity and epitope spreading.
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