类有机物
生物
结直肠癌
外周血
癌症
癌症研究
循环肿瘤细胞
免疫学
癌细胞
肺癌
细胞生物学
病理
医学
转移
遗传学
作者
Krijn K. Dijkstra,Chiara M. Cattaneo,Fleur Weeber,Myriam Chalabi,Joris van de Haar,Lorenzo F. Fanchi,Maarten Slagter,Daphne van der Velden,Sovann Kaing,Sander Kelderman,Nienke van Rooij,Monique E. van Leerdam,Annekatrien Depla,Egbert F. Smit,Koen J. Hartemink,Rosa de Groot,Monika C. Wolkers,Norman Sachs,Pétur Snæbjörnsson,Kim Monkhorst
出处
期刊:Cell
[Cell Press]
日期:2018-08-09
卷期号:174 (6): 1586-1598.e12
被引量:1067
标识
DOI:10.1016/j.cell.2018.07.009
摘要
Cancer immunotherapies have shown substantial clinical activity for a subset of patients with epithelial cancers. Still, technological platforms to study cancer T-cell interactions for individual patients and understand determinants of responsiveness are presently lacking. Here, we establish and validate a platform to induce and analyze tumor-specific T cell responses to epithelial cancers in a personalized manner. We demonstrate that co-cultures of autologous tumor organoids and peripheral blood lymphocytes can be used to enrich tumor-reactive T cells from peripheral blood of patients with mismatch repair-deficient colorectal cancer and non-small-cell lung cancer. Furthermore, we demonstrate that these T cells can be used to assess the efficiency of killing of matched tumor organoids. This platform provides an unbiased strategy for the isolation of tumor-reactive T cells and provides a means by which to assess the sensitivity of tumor cells to T cell-mediated attack at the level of the individual patient.
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