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Endothelial, pericyte and tumor cell expression in glioblastoma identifies fibroblast activation protein (FAP) as an excellent target for immunotherapy
Clinical & Translational Immunology ( IF 4.6 ) Pub Date : 2020-10-14 , DOI: 10.1002/cti2.1191
Lisa M Ebert 1, 2 , Wenbo Yu 1 , Tessa Gargett 1, 2 , John Toubia 1 , Paris M Kollis 1, 2 , Melinda N Tea 1 , Brenton W Ebert 1 , Cedric Bardy 3, 4 , Mark van den Hurk 3, 4 , Claudine S Bonder 1, 2 , Jim Manavis 2 , Kathleen S Ensbey 5 , Mariana Oksdath Mansilla 1 , Kaitlin G Scheer 1, 6 , Sally L Perrin 1, 6 , Rebecca J Ormsby 4 , Santosh Poonnoose 4, 7 , Barbara Koszyca 8 , Stuart M Pitson 1, 2 , Bryan W Day 5, 9, 10 , Guillermo A Gomez 1 , Michael P Brown 1, 2, 11
Affiliation  

Targeted immunotherapies such as chimeric antigen receptor (CAR)‐T cells are emerging as attractive treatment options for glioblastoma, but rely on identification of a suitable tumor antigen. We validated a new target antigen for glioblastoma, fibroblast activation protein (FAP), by undertaking a detailed expression study of human samples.

中文翻译:

胶质母细胞瘤中的内皮细胞、周细胞和肿瘤细胞表达将成纤维细胞活化蛋白 (FAP) 鉴定为免疫治疗的极好靶点

嵌合抗原受体 (CAR)-T 细胞等靶向免疫疗法正在成为胶质母细胞瘤的有吸引力的治疗选择,但依赖于合适的肿瘤抗原的鉴定。我们通过对人类样本进行详细的表达研究,验证了胶质母细胞瘤的新靶抗原成纤维细胞活化蛋白 (FAP)。
更新日期:2020-10-16
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