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Isolation and Expansion of Cytotoxic Cytokine-induced Killer T Cells for Cancer Treatment
Published on: January 24, 2020
Overcoming the limitations of cytokines to improve cancer therapy
Claudia Augusta Di Trani1, Assunta Cirella1, Leire Arrizabalaga1
1Program of Immunology and Immunotherapy, Cima Universidad de Navarra, Pamplona, Spain; Navarra Institute for Health Research (IDISNA), Pamplona, Spain.
Abstract:
Cytokines are pleiotropic soluble proteins used by immune cells to orchestrate a coordinated response against pathogens and malignancies. In cancer immunotherapy, cytokine-based drugs can be developed potentiating pro-inflammatory cytokines or blocking immunosuppressive cytokines. However, the complexity of the mechanisms of action of cytokines requires the use of biotechnological strategies to minimize systemic toxicity, while potentiating the antitumor response. Sequence mutagenesis, fusion proteins and gene therapy strategies are employed to enhance the half-life in circulation, target the desired bioactivity to the tumor microenvironment, and to optimize the therapeutic window of cytokines. In this review, we provide an overview of the different strategies currently being pursued in pre-clinical and clinical studies to make the most of cytokines for cancer immunotherapy.
Insights
Cytokines are key for immune responses. Biotechnological strategies are enhancing their use in cancer immunotherapy by improving delivery and reducing side effects for better antitumor activity.
Area of Science:
- Immunology
- Biotechnology
- Oncology
Background:
- Cytokines are crucial soluble proteins mediating immune cell communication.
- They play a vital role in orchestrating responses against pathogens and cancer.
- Cytokine-based drugs are explored for cancer immunotherapy by modulating pro-inflammatory or immunosuppressive cytokines.
Purpose of the Study:
- To review current biotechnological strategies for optimizing cytokine-based cancer immunotherapy.
- To highlight methods for enhancing cytokine efficacy and minimizing systemic toxicity.
- To provide an overview of pre-clinical and clinical applications of these strategies.
Main Methods:
- Review of literature on cytokine engineering and delivery systems.
- Analysis of sequence mutagenesis, fusion proteins, and gene therapy applications.
- Examination of strategies to improve half-life, tumor targeting, and therapeutic window.
Main Results:
- Biotechnological approaches can enhance cytokine circulation half-life.
- Strategies exist to specifically target cytokine bioactivity to the tumor microenvironment.
- Optimizing cytokine delivery improves the therapeutic window for cancer treatment.
Conclusions:
- Advanced biotechnological strategies are essential for effective cytokine-based cancer immunotherapy.
- These methods offer promise in overcoming challenges of systemic toxicity and improving antitumor responses.
- Continued research in pre-clinical and clinical settings is vital to fully harness cytokine potential in oncology.
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