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Updated: May 31, 2026

Merkel Cell Polyomavirus Infection and Detection
Published on: February 7, 2019
Merkel cell polyomavirus infection and Merkel cell carcinoma in HIV-positive individuals
Ulrike Wieland1, Alexander Kreuter
1Institute of Virology, National Reference Centre for Papilloma- and Polyomaviruses, University of Cologne, Koeln, Germany. ulrike.wieland@uni-koeln.de
Purpose Of Review:
Merkel cell polyomavirus (MCPyV) was recently discovered in Merkel cell carcinoma (MCC), an aggressive nonmelanoma skin tumour. MCC incidence has been rising in the last decades. Immunocompromised individuals such as HIV-infected patients have an increased risk for MCC development.
Recent Findings:
MCPyV is found--mostly integrated into the host genome--in approximately 80% of MCC. The causal role of MCPyV in MCC development has been corroborated by several recent studies. Cutaneous MCPyV infection is acquired early in life and is widespread in the general population. In HIV-positive patients, MCPyV-DNA has been detected on the skin, on oral and anogenital mucosa, and in plucked eyebrow-hairs. Compared with healthy controls, MCPyV prevalence is increased in HIV-infected individuals and severe HIV-related immunosuppression is associated with elevated cutaneous MCPyV-DNA loads. This could explain the increased MCC risk found in HIV-infected individuals. MCC in HIV-infected patients occurs at a relatively young age and frequently on sites not exposed to sunlight.
Summary:
Guidelines for screening and early detection of MCC should be developed for HIV-positive patients. Future studies should evaluate changes in MCC incidence rates in HIV-infected individuals and analyse the effect of immune restoration by (early) antiretroviral therapy on MCC incidence and on cutaneous MCPyV load.
Insights
Merkel cell polyomavirus (MCPyV) is linked to Merkel cell carcinoma (MCC) in HIV-positive individuals. Increased MCPyV prevalence and DNA load in immunocompromised patients may explain their higher MCC risk.
Area of Science:
- Oncology
- Virology
- Dermatology
Background:
- Merkel cell carcinoma (MCC) is an aggressive skin cancer with rising incidence.
- Merkel cell polyomavirus (MCPyV) is a recently identified cause of MCC.
- HIV-infected individuals have an elevated risk for developing MCC.
Purpose of the Study:
- To review the role of MCPyV in MCC development, particularly in HIV-infected individuals.
- To highlight the increased prevalence and viral load of MCPyV in immunocompromised populations.
- To discuss implications for MCC screening and management in HIV patients.
Main Methods:
- Review of recent studies on MCPyV and MCC.
- Analysis of MCPyV prevalence and DNA detection in various body sites.
- Comparison of MCPyV status between HIV-infected individuals and healthy controls.
Main Results:
- MCPyV is present in approximately 80% of MCC cases, often integrated into the host genome.
- MCPyV infection is common in the general population, acquired early in life.
- HIV-infected individuals show increased MCPyV prevalence and higher cutaneous viral loads, especially with severe immunosuppression.
- MCC in HIV patients often occurs at a younger age and on non-sun-exposed skin.
Conclusions:
- The causal role of MCPyV in MCC development is supported by current evidence.
- Elevated MCPyV loads in HIV-infected individuals may contribute to their increased MCC risk.
- Development of screening and early detection guidelines for MCC in HIV-positive patients is recommended.
- Further research should investigate MCC incidence trends in HIV patients and the impact of antiretroviral therapy on MCPyV load and MCC risk.
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