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Updated: Dec 22, 2025

Utilizing the Antigen Capsid-Incorporation Strategy for the Development of Adenovirus Serotype 5-Vectored Vaccine Approaches
Published on: May 6, 2015
Expanding the Spectrum of Adenoviral Vectors for Cancer Therapy
Jian Gao1, Wenli Zhang1, Anja Ehrhardt1
1Institute for Virology and Microbiology, Center for Biomedical Education and Research (ZBAF), Department of Human Medicine, Faculty of Health, Witten/Herdecke University, 58453 Witten, Germany.
Abstract:
Adenoviral vectors (AdVs) have attracted much attention in the fields of vaccine development and treatment for diseases such as genetic disorders and cancer. In this review, we discuss the utility of AdVs in cancer therapies. In recent years, AdVs were modified as oncolytic AdVs (OAs) that possess the characteristics of cancer cell-specific replication and killing. Different carriers such as diverse cells and extracellular vesicles are being explored for delivering OAs into cancer sites after systemic administration. In addition, there are also various strategies to improve cancer-specific replication of OAs, mainly through modifying the early region 1 (E1) of the virus genome. It has been documented that oncolytic viruses (OVs) function through stimulating the immune system, resulting in the inhibition of cancer progression and, in combination with classical immune modulators, the anti-cancer effect of OAs can be even further enforced. To enhance the cancer treatment efficacy, OAs are also combined with other standard treatments, including surgery, chemotherapy and radiotherapy. Adenovirus type 5 (Ad5) has mainly been explored to develop vectors for cancer treatment with different modulations. Only a limited number of the more than 100 identified AdV types were converted into OAs and, therefore, the construction of an adenovirus library for the screening of potential novel OA candidates is essential. Here, we provide a state-of-the-art overview of currently performed and completed clinic trials with OAs and an adenovirus library, providing novel possibilities for developing innovative adenoviral vectors for cancer treatment.
Insights
Oncolytic adenoviral vectors (OAs) show promise for cancer treatment by selectively replicating within and killing cancer cells. Further research into novel OA candidates and delivery systems is essential for advancing cancer therapies.
Area of Science:
- Oncology
- Virology
- Gene Therapy
Background:
- Adenoviral vectors (AdVs) are widely investigated for therapeutic applications, including cancer treatment.
- Oncolytic AdVs (OAs) are engineered to specifically replicate in and lyse cancer cells.
- Current research explores novel delivery methods and genetic modifications to enhance OA efficacy.
Purpose of the Study:
- To review the current applications and advancements of adenoviral vectors in cancer therapy.
- To highlight the development and potential of oncolytic adenoviruses (OAs) as a cancer treatment modality.
- To provide an overview of clinical trials and future directions for adenoviral vector-based cancer therapies.
Main Methods:
- Review of existing literature on adenoviral vectors and their use in cancer treatment.
- Analysis of strategies for modifying adenoviral genomes to enhance oncolytic activity.
- Examination of clinical trial data for oncolytic viruses and adenoviral libraries.
Main Results:
- OAs demonstrate cancer cell-specific replication and cell-killing capabilities.
- Delivery systems including cells and extracellular vesicles are being explored for targeted OA delivery.
- Combining OAs with immunotherapy and standard cancer treatments enhances anti-cancer effects.
Conclusions:
- Adenoviral vectors, particularly OAs, represent a promising strategy for cancer treatment.
- Further development of an adenovirus library is crucial for identifying novel OA candidates.
- Clinical trials indicate the potential of OAs in cancer therapy, with ongoing research focused on improving efficacy and delivery.
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