体内
免疫系统
纤维化
卵清蛋白
抗原
病态的
细胞
癌症研究
电池类型
免疫学
医学
生物
病理
遗传学
生物技术
作者
Jieqiong Zhang,Tatsuya Tsukui,Xiumin Wu,Alyssa Brito,John Maxwell Trumble,Juan C Caraballo,Greg M Allen,Jose Zavala-Solorio,Chunlian Zhang,Jonathan Paw,Wendell A. Lim,Jiefei Geng,Yuliya Kutskova,Adam Freund,Ganesh Kolumam,Dean Sheppard,Robert L Cohen
标识
DOI:10.26508/lsa.202201869
摘要
Immunological targeting of pathological cells has been successful in oncology and is expanding to other pathobiological contexts. Here, we present a flexible platform that allows labeling cells of interest with the surface-expressed model antigen ovalbumin (OVA), which can be eliminated via either antigen-specific T cells or newly developed OVA antibodies. We demonstrate that hepatocytes can be effectively targeted by either modality. In contrast, pro-fibrotic fibroblasts associated with pulmonary fibrosis are only eliminated by T cells in initial experiments, which reduced collagen deposition in a fibrosis model. This new experimental platform will facilitate development of immune-based approaches to clear potential pathological cell types in vivo.
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