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Updated: Jul 1, 2026

Generation of Multivirus-specific T Cells to Prevent/treat Viral Infections after Allogeneic Hematopoietic Stem Cell Transplant
Published on: May 27, 2011
Molecular concepts of virus infections causing skin cancer in organ transplant recipients
1DKFZ-Charité Cooperation, Viral Skin Carcinogenesis, German Cancer Research Center, Heidelberg, Germany. i.nindl@dkfz.de
Abstract:
Globally approximately 15% of all malignant tumors are caused by viruses and even a higher percentage is observed in organ transplant recipients (OTR). Here, nonmelanoma skin cancer (NMSC) is the most frequent malignancy, which correlates with cutaneous human papilloma virus (HPV) infection. In the present review, we reflect on some recent general concepts how tumor viruses can either act as direct or indirect carcinogens in the multistep process of carcinogenesis. Immunosuppressive drugs in OTR, which reduce the risk of organ rejection, could be critical in increasing the activation of persisting viral infections, thereby enhancing the probability to develop skin tumors. We discuss virus-induced transformation with special emphasis on the function of HPV as an indirect and HHV-8 as direct carcinogen in the development of NMSC and Kaposi sarcoma (KS), respectively. Moreover, we describe a rodent model system useful to examine future strategies in preventing skin tumor formation in immunosuppressed OTR.
Insights
Viruses cause 15% of cancers, especially in organ transplant recipients (OTR) due to immunosuppression. This review explores how viruses like human papillomavirus (HPV) drive skin cancer development in OTR.
Area of Science:
- Oncology
- Virology
- Immunology
Background:
- Viruses are responsible for approximately 15% of all malignant tumors globally.
- This percentage is significantly higher in organ transplant recipients (OTRs).
- Nonmelanoma skin cancer (NMSC) is the most common malignancy in OTRs, often linked to cutaneous human papillomavirus (HPV) infection.
Purpose of the Study:
- To review general concepts of viral carcinogenesis, focusing on direct and indirect mechanisms.
- To discuss the role of immunosuppressive drugs in OTRs and their impact on viral infections and skin tumor development.
- To highlight the specific roles of HPV and HHV-8 in NMSC and Kaposi sarcoma (KS), respectively.
Main Methods:
- Review of current literature on viral carcinogenesis.
- Discussion of the mechanisms of virus-induced transformation.
- Description of a rodent model for studying skin tumor prevention strategies.
Main Results:
- Tumor viruses can act as direct or indirect carcinogens in multistep carcinogenesis.
- Immunosuppression in OTRs can reactivate latent viral infections, increasing skin tumor risk.
- HPV functions as an indirect carcinogen, while HHV-8 acts as a direct carcinogen in specific cancers.
Conclusions:
- Understanding viral carcinogenesis is crucial for managing cancer risk in OTRs.
- Targeting viral reactivation and oncogenic pathways may offer preventative strategies.
- Rodent models are valuable for testing novel approaches to prevent skin tumors in immunosuppressed populations.
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