免疫系统
CD8型
细胞毒性T细胞
癌症研究
胞外囊泡
T细胞
生物
抗原
免疫学
医学
微泡
体外
小RNA
生物化学
基因
作者
Travis J. Gates,Dechen Wangmo,Xianda Zhao,Subbaya Subramanian
标识
DOI:10.1016/j.omto.2023.100727
摘要
Most colorectal cancer (CRC) patients present with a microsatellite-stable phenotype, rendering them resistant to immune checkpoint inhibitors (ICIs). Among the contributors to ICI resistance, tumor-derived extracellular vesicles (TEVs) have emerged as critical players. Previously we demonstrated that autologous transfer of TEVs without miR-424 can induce tumor antigen-specific immune responses in CRC models. Therefore, we postulated that allogeneic TEVs, modified to lack miR-424 and derived from an MC38 cells, could induce CD8
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