Tumor endothelial marker 1-specific DNA vaccination targets tumor vasculature

被引:61
|
作者
Facciponte, John G. [1 ]
Ugel, Stefano [1 ]
De Sanctis, Francesco [1 ,2 ]
Li, Chunsheng [1 ]
Wang, Liping [3 ]
Nair, Gautham [4 ]
Sehgal, Sandy [5 ]
Raj, Arjun [4 ]
Matthaiou, Efthymia [1 ]
Coukos, George [1 ]
Facciabene, Andrea [1 ]
机构
[1] Univ Penn, Sch Med, OCRC, Philadelphia, PA 19104 USA
[2] Univ Perugia, Dept Expt Med & Biochem Sci, I-06100 Perugia, Italy
[3] Univ Penn, Dept Pathol & Lab Med, Philadelphia, PA USA
[4] Univ Penn, Dept Bioengn, Philadelphia, PA 19104 USA
[5] Univ Penn, Dept Radiol, Philadelphia, PA 19104 USA
来源
JOURNAL OF CLINICAL INVESTIGATION | 2014年 / 124卷 / 04期
关键词
WOUND-HEALING COMPLICATIONS; T-CELL RESPONSES; GROWTH-FACTOR; CARCINOEMBRYONIC ANTIGEN; ENDOSIALIN TEM1; STROMAL FIBROBLASTS; CRITICAL COMPONENTS; PROTEIN EXPRESSION; CANCER; ANGIOGENESIS;
D O I
10.1172/JCI67382
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
收藏
页码:1497 / 1511
页数:15
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