Lymphotropism of merkel cell polyomavirus infection, Nova Scotia, Canada

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Abstract

To test the hypothesis that Merkel cell polyomavirus (MCPyV) can infect cells of the lymphoid system, we analyzed 353 specimens, including 152 non-Hodgkin lymphomas, 44 Hodgkin lymphomas, 110 benign lymph nodes, 27 lymph nodes with metastasis, and 20 extranodal tissue samples. MCPyV DNA was detected by quantitative PCR in 13 (6.6%) of 196 lymphomas, including 5 (20.8%) of 24 chronic lymphocytic leukemia specimens, and in 11 (10%) of 110 benign lymph nodes, including 8 (13.1%) of 61 samples of reactive hyperplasia and 3 (10.3%) of 29 normal lymph nodes. Other samples were MCPyV negative. Sequence analysis of 9 virus-positive samples confirmed the identity of MCPyV; 3 viral strains were represented. Immunohistochemical testing showed that 1 T-cell lymphoma expressed MCPyV T-antigen. These findings suggest that the lymphoid system plays a role in MCPyV infection and may be a site for MCPyV persistence.

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Toracchio, S., Foyle, A., Sroller, V., Reed, J. A., Wu, J., Kozinetz, C. A., & Butel, J. S. (2010). Lymphotropism of merkel cell polyomavirus infection, Nova Scotia, Canada. Emerging Infectious Diseases, 16(11), 1702–1709. https://doi.org/10.3201/eid1611.100628

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