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以 STEAP1 CAR-T 细胞和肿瘤局部 IL-12 免疫疗法靶向晚期前列腺癌

英文原题:Targeting advanced prostate cancer with STEAP1 chimeric antigen receptor T cell and tumor-localized IL-12 immunotherapy.

PubMed 2023/04/11(内容时间) Nat Commun Q1 · IF 18.1(JCR 2025)

研究概要

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。

中文摘要

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。

展开英文摘要原文

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.

论文信息

作者
Bhatia V、Kamat NV、Pariva TE、Wu LT、Tsao A、Sasaki K、Sun H、Javier G
第一作者单位
Human Biology Division, Fred Hutchinson Cancer Center, 1100 Fairview Ave N, Seattle, WA, 98109, USA.United States
通讯作者单位
Human Biology Division, Fred Hutchinson Cancer Center, 1100 Fairview Ave N, Seattle, WA, 98109, USA. jklee5@fredhutch.org.United States
文献类型
非美国政府资助研究 · 美国政府(非公共卫生署)资助研究 · 美国 NIH 资助研究
期刊
Nature communications2023 Apr 11
原文标识
PubMed 37041154 · DOI 10.1038/s41467-023-37874-2