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Published on: October 5, 2015
Treating Adenovirus Infection in Transplant Populations: Therapeutic Options Beyond Cidofovir?
Niyati Narsana1, David Ha2,3, Dora Y Ho3
1Division of Infectious Diseases, UC Davis Medical Center, Sacramento, CA 95817, USA.
Abstract:
Adenovirus (AdV) infections can lead to significant morbidity and increased mortality in immunocompromised populations such as hematopoietic stem cell and solid organ transplant recipients. This review evaluates currently available and emerging therapies for AdV infections. Cidofovir, while most commonly used, is limited by its variable efficacy and nephrotoxicity. This led to the development of brincidofovir, which has a better safety profile and great in vitro potency against AdV. The use of ribavirin and ganciclovir has been reported in the literature, but their use is limited due to inconsistent efficacy. Immune-based approaches, such as adoptive T-cell therapy, have shown promise in achieving viral clearance and improving survival but remain constrained by challenges related to manufacturing complexity and risks of graft-versus-host disease. This review underscores the need for standardized treatment protocols as well as comparative studies to identify optimal dosing and timing to initiate treatment. Future research should focus on individualized treatment approaches and the development of novel therapeutic agents to address the unmet clinical needs of AdV management.
Insights
Adenovirus infections pose serious risks to transplant patients. This review examines current and new treatments, highlighting the need for better therapies and standardized protocols for managing adenovirus (AdV) in immunocompromised individuals.
Area of Science:
- Virology
- Immunology
- Pharmacology
Background:
- Adenovirus (AdV) infections cause significant illness and death in immunocompromised patients, particularly transplant recipients.
- Current treatments like cidofovir have limitations including variable effectiveness and toxicity.
- Existing antiviral drugs (ribavirin, ganciclovir) show inconsistent efficacy against AdV.
Purpose of the Study:
- To review and evaluate existing and emerging therapies for adenovirus infections.
- To identify challenges and unmet needs in AdV management for immunocompromised populations.
- To highlight the need for improved treatment strategies and further research.
Main Methods:
- Systematic review of current and emerging AdV therapies.
- Analysis of clinical data on antiviral drugs and immune-based approaches.
- Evaluation of safety profiles and efficacy of different treatment modalities.
Main Results:
- Brincidofovir shows promise with a better safety profile and in vitro potency compared to cidofovir.
- Adoptive T-cell therapy demonstrates potential for viral clearance but faces manufacturing and safety hurdles.
- Existing therapies like ribavirin and ganciclovir have limited efficacy.
Conclusions:
- There is a critical need for standardized treatment protocols and comparative studies for AdV infections.
- Individualized treatment approaches and novel therapeutic agents are essential for effective AdV management.
- Further research is required to address the unmet clinical needs in adenovirus management.
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