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Expression of Exogenous Cytokine in Patient-derived Xenografts via Injection with a Cytokine-transduced Stromal Cell Line
Published on: May 10, 2017
Gene vectors for cytokine expression in vivo
1McMaster University, Department of Pathology and Molecular Medicine, HSC-4H30C, Hamilton, Ontario, L8N 3Z5, Canada. hittma@mcmaster.ca
Abstract:
The understanding of cytokine networks and the exploitation of these networks for the treatment of immune and inflammatory diseases as well as cancer depend on in vivo delivery of cytokines. Due to instability of recombinant cytokine proteins, investigators have employed cytokine-encoding gene therapy vectors to induce high levels of cytokine expression in vivo. Numerous gene therapy vectors have been developed recently which are suitable for this purpose. Recent advances in the design of adenovirus, adeno-associated virus, poxvirus, retrovirus, lentivirus, and nonviral vectors are described here. Properties of the various vector systems which determine their usefulness for cytokine gene delivery are compared. The implementations of cytokine-encoding gene therapy vectors for analyzing immune responses and for the therapy of inflammatory disorders, immune disease, infections and cancer are reviewed.
Insights
Gene therapy vectors deliver cytokines in vivo for treating diseases like cancer and immune disorders. Advances in viral and nonviral vectors are reviewed for effective cytokine gene delivery and therapeutic applications.
Area of Science:
- Immunology
- Gene Therapy
- Molecular Biology
Background:
- Cytokines are crucial for immune responses, but their instability limits therapeutic use.
- Gene therapy offers a solution by enabling in vivo cytokine expression.
- Developing effective delivery systems is key for treating immune and inflammatory diseases and cancer.
Purpose of the Study:
- To review recent advances in cytokine-encoding gene therapy vectors.
- To compare the properties of various vector systems for cytokine gene delivery.
- To discuss the applications of these vectors in research and therapy.
Main Methods:
- Review of recent developments in adenovirus, adeno-associated virus, poxvirus, retrovirus, lentivirus, and nonviral vectors.
- Comparative analysis of vector system properties relevant to in vivo cytokine gene delivery.
- Summary of implemented strategies for immune response analysis and disease therapy.
Main Results:
- Numerous gene therapy vectors have been developed for in vivo cytokine expression.
- Adenovirus, AAV, poxvirus, retrovirus, lentivirus, and nonviral vectors show promise.
- Vector properties vary, influencing their suitability for specific gene delivery applications.
Conclusions:
- Cytokine gene therapy vectors are essential tools for understanding and treating immune-related diseases and cancer.
- Ongoing advancements in vector design enhance their therapeutic potential.
- Effective in vivo cytokine delivery via gene therapy holds significant promise for diverse clinical applications.
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