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Microfluidic Co-Culture Models for Dissecting the Immune Response in in vitro Tumor Microenvironments
Published on: April 30, 2021
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Microfluidic models for adoptive cell-mediated cancer immunotherapies
Giulia Adriani1, Andrea Pavesi1, Anthony T Tan2
1Singapore-MIT Alliance for Research and Technology, BioSyM IRG, 1 Create Way, 138602, Singapore.
Drug Discovery Today
|May 18, 2016
Summary
Three-dimensional (3D) microfluidic tumor models can accelerate cancer immunotherapy development. These models help test engineered T cells and combination therapies, improving treatment efficacy and clinical translation.
Area of Science:
- Oncology
- Immunology
- Biotechnology
Background:
- Adoptive T cell therapy shows promise for cancer treatment but requires further optimization.
- The tumor microenvironment significantly influences immunotherapy outcomes.
- Current preclinical models have limitations in accurately predicting clinical efficacy.
Purpose of the Study:
- To explore the utility of 3D microfluidic tumor models for evaluating T cell immunotherapies.
- To assess the potential of these models in identifying effective combination therapies.
- To facilitate the clinical translation of T cell-based cancer treatments.
Main Methods:
- Development and utilization of 3D microfluidic systems that mimic the tumor microenvironment.
- Assessment of engineered T cell function within these models.
- Screening of various therapeutic combinations to evaluate synergistic effects.
Main Results:
- 3D microfluidic models effectively recapitulate key aspects of the tumor microenvironment.
- These models allow for robust assessment of engineered T cell efficacy.
- Potential combinatorial therapies can be identified to enhance treatment outcomes.
Conclusions:
- 3D microfluidic tumor models offer a powerful platform for advancing T cell cancer immunotherapy.
- These systems can accelerate the screening of patient-specific treatments.
- This approach promises to reduce reliance on in vivo studies and speed up clinical translation.

