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Generation of Tumor-Reactive T Cells by Co-culture of Peripheral Blood Lymphocytes and Tumor Organoids.

Krijn K Dijkstra ,
Chiara M Cattaneo ,
Fleur Weeber ,
Myriam Chalabi ,
Joris van de Haar ,
Lorenzo F Fanchi ,
Maarten Slagter ,
Daphne L 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 ,
Petur Snaebjornsson ,
Kim Monkhorst ,
John Haanen ,
Hans Clevers ,
Ton N Schumacher ,
Emile E Voest

Abstract

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.

More about this publication

Cell

Volume 174
Issue nr. 6
Pages 1586-1598.e12
Publication date 06-09-2018

Full text links

Publisher website (DOI) 10.1016/j.cell.2018.07.009
Europe PubMed Central 30100188
Pubmed 30100188

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