Related Experiment Video
Updated: Dec 16, 2025

12:42
Paramyxoviruses for Tumor-targeted Immunomodulation: Design and Evaluation Ex Vivo
Published on: January 7, 2019
10.0K
Optimizing Oncolytic Viral Design to Enhance Antitumor Efficacy: Progress and Challenges
Shyambabu Chaurasiya1, Yuman Fong1, Susanne G Warner1
1Department of Surgery, City of Hope National Medical Center, Duarte, CA 91010, USA.
Cancers
|July 2, 2020
Summary
Oncolytic virotherapy shows promise but needs improved efficacy, especially in challenging tumors. Arming viruses with immune-modulating transgenes offers a promising strategy to enhance cancer treatment outcomes.
Area of Science:
- Oncology
- Virology
- Immunotherapy
Background:
- Oncolytic virotherapy has advanced, with approved treatments like Talimogene Laherparepvec for melanoma.
- While generally safe, oncolytic viruses show inconsistent efficacy, particularly in immunosuppressed tumors.
- Improving oncolytic virus effectiveness is crucial for broader clinical application.
Purpose of the Study:
- To review progress in arming oncolytic viruses, focusing on immune-modulatory transgenes.
- To discuss strategies for enhancing oncolytic virus therapy.
- To identify challenges for the clinical use of armed oncolytic viruses.
Main Methods:
- Review of preclinical and clinical studies on oncolytic viruses.
- Analysis of transgene-arming strategies for oncolytic viruses.
- Focus on immune-modulatory and tumor-stroma-modulating transgenes.
Main Results:
- Oncolytic viruses can be armed with transgenes to enhance therapeutic efficacy.
- Immune-modulatory transgenes are frequently used to boost anti-tumor immune responses.
- Transgenes can also modulate the tumor microenvironment and aid in imaging.
Conclusions:
- Arming oncolytic viruses with transgenes, particularly immune-modulators, is a key strategy to improve cancer treatment.
- Further research is needed to overcome challenges and facilitate widespread clinical adoption of armed oncolytic viruses.
Related Concept Videos
Tumor Immunotherapy
1.6K
Immunotherapy is a treatment that boosts or manipulates the immune system to fight diseases, including cancer. For instance, by stimulating an immune response through vaccinations against viruses that cause cancers, like hepatitis B virus and human papillomavirus, these diseases can be prevented. Nonetheless, some cancer cells can avoid the immune system due to their rapid mutation and division. The immune response to many cancers involves three phases: elimination, equilibrium, and escape.
1.6K
Cancer Therapies
9.7K
Cancer therapies are various modes of treatment, such as surgery, radiation therapy, and chemotherapy that are administered to cancer patients.
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
9.7K
Microorganisms in Medicine and Therapeutics
801
Microorganisms play a fundamental role in vaccine development, gene therapy, and therapeutic production. Their biological properties are harnessed to advance medicine and public health. Beyond immunization, microorganisms contribute to gut health, antibiotic synthesis, and genetic disease treatment.Live Attenuated and Inactivated VaccinesLive attenuated vaccines, such as the measles, mumps, and rubella (MMR) vaccine, utilize weakened forms of pathogens to closely resemble natural infections.
801
Mechanisms of Retrovirus-induced Cancers
6.7K
Retroviruses are RNA viruses that have been shown to cause cancers in diverse species, including chickens, mice, cats, and monkeys. The RNA genomes of these viruses are first reverse-transcribed into single and then double-stranded DNA (dsDNA) copies. This dsDNA called proviral DNA then integrates into the host genome. Subsequently, the host cell transcribes the proviral DNA in concert with the chromosomal DNA. This leads to the production of viral RNA and proteins that assemble at the host...
6.7K

