J Clin Invest. 2014 Apr;124(4):1497-511. doi: 10.1172/JCI67382. Epub 2014 Mar 18.
Tumor endothelial marker 1 (TEM1; also known as endosialin or CD248) is a protein found on tumor vasculature and in tumor stroma. Here, we tested whether TEM1 has potential as a therapeutic target for cancer immunotherapy by immunizing immunocompetent mice with Tem1 cDNA fused to the minimal domain of the C fragment of tetanus toxoid (referred to herein as Tem1-TT vaccine). Tem1-TT vaccination elicited CD8+ and/or CD4+ T cell responses against immunodominant TEM1 protein sequences. Prophylactic immunization of animals with Tem1-TT prevented or delayed tumor formation in several murine tumor models. Therapeutic vaccination of tumor-bearing mice reduced tumor vascularity, increased infiltration of CD3+ T cells into the tumor, and controlled progression of established tumors. Tem1-TT vaccination also elicited CD8+ cytotoxic T cell responses against murine tumor-specific antigens. Effective Tem1-TT vaccination did not affect angiogenesis-dependent physiological processes, including wound healing and reproduction. Based on these data and the widespread expression of TEM1 on the vasculature of different tumor types, we conclude that targeting TEM1 has therapeutic potential in cancer immunotherapy.
肿瘤内皮标志物 1(TEM1;也称为内唾液酸素或 CD248)是一种存在于肿瘤血管和肿瘤基质中的蛋白质。在这里,我们通过用破伤风类毒素 C 片段的最小域融合的 Tem1 cDNA 免疫免疫功能正常的小鼠来测试 TEM1 是否有可能成为癌症免疫治疗的治疗靶点(在此称为 Tem1-TT 疫苗)。Tem1-TT 疫苗接种引发了针对免疫优势 TEM1 蛋白序列的 CD8+和/或 CD4+T 细胞反应。用 Tem1-TT 预防性免疫接种可预防或延迟几种小鼠肿瘤模型中的肿瘤形成。对荷瘤小鼠进行治疗性疫苗接种可减少肿瘤血管生成,增加 CD3+T 细胞浸润肿瘤,并控制已建立的肿瘤进展。Tem1-TT 疫苗接种还引发了针对小鼠肿瘤特异性抗原的 CD8+细胞毒性 T 细胞反应。有效的 Tem1-TT 疫苗接种不会影响依赖血管生成的生理过程,包括伤口愈合和繁殖。基于这些数据和不同肿瘤类型血管中 TEM1 的广泛表达,我们得出结论,靶向 TEM1 在癌症免疫治疗中有治疗潜力。