Loading…

In vitro humanized 3D microfluidic chip for testing personalized immunotherapeutics for head and neck cancer patients

Immunotherapy and personalized medicine therapeutics are emerging as promising approaches in the management of head and neck squamous cell carcinoma (HNSCC). In spite of that, there is yet no assay that could predict individual response to immunotherapy. We manufactured an in vitro 3D microfluidic c...

Full description

Saved in:
Bibliographic Details
Published in:Experimental cell research 2019-10, Vol.383 (2), p.111508-111508, Article 111508
Main Authors: Al-Samadi, Ahmed, Poor, Benedek, Tuomainen, Katja, Liu, Ville, Hyytiäinen, Aini, Suleymanova, Ilida, Mesimaki, Karri, Wilkman, Tommy, Mäkitie, Antti, Saavalainen, Päivi, Salo, Tuula
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Immunotherapy and personalized medicine therapeutics are emerging as promising approaches in the management of head and neck squamous cell carcinoma (HNSCC). In spite of that, there is yet no assay that could predict individual response to immunotherapy. We manufactured an in vitro 3D microfluidic chip to test the efficacy of immunotherapy. The assay was first tested using a tongue cancer cell line (HSC-3) embedded in a human tumour-derived matrix “Myogel/fibrin” and immune cells from three healthy donors. Next, the chips were used with freshly isolated cancer cells, patients' serum and immune cells. Chips were loaded with different immune checkpoint inhibitors, PD-L1 antibody and IDO 1 inhibitor. Migration of immune cells towards cancer cells and the cancer cell proliferation rate were evaluated. Immune cell migration towards HSC-3 cells was cancer cell density dependent. IDO 1 inhibitor induced immune cells to migrate towards cancer cells both in HSC-3 and in two HNSCC patient samples. Efficacy of PD-L1 antibody and IDO 1 inhibitor was patient dependent. We introduced the first humanized in vitro microfluidic chip assay to test immunotherapeutic drugs against HNSCC patient samples. This assay could be used to predict the efficacy of immunotherapeutic drugs for individual patients. •Immunotherapy is emerging as the most promising approaches in cancer treatment.•There is no personalized assay that can predict patient response to immunotherapy.•We introduced fully humanized microfluidic chip to test immunotherapeutic drugs.•The chip is loaded with isolated cancer cells, patients' serum and immune cells.•Several immunotherapeutic drugs can be tested for each patient simultaneously.
ISSN:0014-4827
1090-2422
1090-2422
DOI:10.1016/j.yexcr.2019.111508