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Immunotherapy on Chip: “Under the Microscope” Drug-induced Modulation of the Immune Response
EP25751
Immunotherapy on Chip: “Under the Microscope” Drug-induced Modulation of the Immune Response
Submitted on 18 May 2017

A. De Ninno (a), F. Bertani (a), A. Gerardino (a), F. Mattei (b), V. Lucarini (b), G. Schiavoni (b), S. Parlato (b), L. Gabriele (b), R. Molfetta (f), E. Martinelli (c), A. Mencattini (c), D. Di Giuseppe (c), C. Di Natale (c), G. Kroemer (d), E. Vacchelli (d), A. Rainer (e), S. Giannitelli(e), and L. Businaro(a)
a) CNR-Institute for Photonics and Nanotechnologies- Via Cineto Romano, 42 00156 Rome, Italy // b) Istituto Superiore di Sanità Viale Regina Elena, 299 00161, Rome, Italy c) Dept. Electronic Engineering, University of Rome Tor Vergata, Rome, Italy // d) Metabolomics and Cell Biology Platforms, Gustave Roussy Cancer Campus; Villejuif, France e) Università Campus Bio-Medico di Roma - via Alvaro del Portillo, 21 - 00128 Rome // f) Department of Molecular Medicine “Sapienza” University of Rome, 00161, Rome, Italy
This poster was presented at Organ-on-a-Chip Europe 2017
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Poster Abstract
We present our approach to perform and analyze immune system–cancer cross talk on chip experiments. Flanking in-vivo and in-vitro experiments with on chip co-cultures of primary human PBMC, immune cell subpopulations or murine spleen cells with melanoma, breast and colorectal cancer cells allowed us to test the on-chip model and to extract meaningful kinetics and behavioral data in the microfluidic controlled environments. The experimental setup allowed us to describe the effects of drugs or genetic modifications on the cell population crosstalk, highlighting or confirming important mechanisms in boosting the immune response against cancer. Our vision is that modern microscopy and on chip immune system reconstitution represent the needed bridge to link biology to advanced mathematical methods developed in complex system physics and to numerical simulation, allowing the development of integrated “cybernetic” models able to explore fundamental biology, and to tackle critical issues of drug testing with impact on clinical trials.

1. Chemotherapy-induced antitumor immunity requires formyl peptide receptor 1. Erika Vacchelli, Yuting Ma, Elisa E. Baracco, Antonella Sistigu, David P. Enot, Federico Pietrocola, Heng Yang, Sandy Adjemian, Kariman Chaba, Michaela Semeraro, Michele Signore, Adele De Ninno, Valeria Lucarini, Francesca Peschiaroli, Luca Businaro, Annamaria Gerardino, Gwenola Manic, Thomas Ulas, Patrick Günther, Joachim L. Schultze, Oliver Kepp, Gautier Stoll, Céline Lefebvre, Claire Mulot, Francesca Castoldi, Sylvie Rusakiewicz, Sylvain Ladoire, Lionel Apetoh, José Manuel Bravo San Pedro, Monica Lucattelli, Cécile Delarasse, Valérie Boige, Michel Ducreux, Suzette Delaloge, Christophe Borg, Fabrice André, Giovanna Schiavoni, Ilio Vitale, Pierre Laurent-Puig, Fabrizio Mattei, Laurence Zitvogel, and Guido Kroemer. Science (2015) 350(6263):972-8 DOI:10.1126/science.aad0779.
2. Cancer-driven dynamics of immune cells in a microfluidic environment. Agliari E., Biselli, E., De Ninni A., Schiavoni G., Gabriel
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