J C Sheu1, J Tran1, P L Rady2, H Dao1, S K Tyring2, H P Nguyen1,2,3. 1. Department of Dermatology, Baylor College of Medicine, Houston, TX, U.S.A. 2. Department of Dermatology, McGovern Medical School, Houston, TX, U.S.A. 3. Department of Dermatology, Emory University School of Medicine, Atlanta, GA, U.S.A.
Abstract
BACKGROUND: Human polyomaviruses (HPyVs) are small, nonenveloped, double-stranded DNA viruses that express tumour antigen proteins. Fourteen species of polyomaviruses have been discovered in humans, and since the 2008 discovery of the first cutaneous polyomavirus - Merkel cell polyomavirus (MCPyV) - six more species have been detected in the skin: trichodysplasia spinulosa-associated polyomavirus (TSPyV), HPyV6, HPyV7, HPyV9, HPyV10 and HPyV13. Of these cutaneous species, only MCPyV, TSPyV, HPyV6 and HPyV7 have been definitively associated with diseases of the skin, most commonly in immunocompromised individuals. MCPyV is a predominant aetiology in Merkel cell carcinomas. TSPyV is one of the aetiological factors of trichodysplasia spinulosa. HPyV6 and HPyV7 have been recently linked to pruritic skin eruptions. The roles of HPyV9, HPyV10 and HPyV13 in pathogenesis, if any, are still unknown, but their molecular features have provided some insight into their functional biology. RESULTS: In this review, we summarize the known molecular mechanisms, clinical presentation and targeted therapies of each of the eight cutaneous HPyVs. CONCLUSIONS: We hope that heightened awareness and clinical recognition of HPyVs will lead to increased reports of HPyV-associated diseases and, consequently, a more robust understanding of how to diagnose and treat these conditions.
BACKGROUND:Humanpolyomaviruses (HPyVs) are small, nonenveloped, double-stranded DNA viruses that express tumour antigen proteins. Fourteen species of polyomaviruses have been discovered in humans, and since the 2008 discovery of the first cutaneous polyomavirus - Merkel cell polyomavirus (MCPyV) - six more species have been detected in the skin: trichodysplasia spinulosa-associated polyomavirus (TSPyV), HPyV6, HPyV7, HPyV9, HPyV10 and HPyV13. Of these cutaneous species, only MCPyV, TSPyV, HPyV6 and HPyV7 have been definitively associated with diseases of the skin, most commonly in immunocompromised individuals. MCPyV is a predominant aetiology in Merkel cell carcinomas. TSPyV is one of the aetiological factors of trichodysplasia spinulosa. HPyV6 and HPyV7 have been recently linked to pruritic skin eruptions. The roles of HPyV9, HPyV10 and HPyV13 in pathogenesis, if any, are still unknown, but their molecular features have provided some insight into their functional biology. RESULTS: In this review, we summarize the known molecular mechanisms, clinical presentation and targeted therapies of each of the eight cutaneous HPyVs. CONCLUSIONS: We hope that heightened awareness and clinical recognition of HPyVs will lead to increased reports of HPyV-associated diseases and, consequently, a more robust understanding of how to diagnose and treat these conditions.
Authors: Rossybelle P Amorrortu; Yayi Zhao; Neil A Fenske; Basil S Cherpelis; Jane L Messina; Anna R Giuliano; Vernon K Sondak; Michael J Schell; Sandrine Mckay-Chopin; Tarik Gheit; Tim Waterboer; Massimo Tommasino; Dana E Rollison Journal: J Infect Dis Date: 2022-09-28 Impact factor: 7.759
Authors: Kathleen M Egan; Youngchul Kim; Noemi Bender; James M Hodge; Anna E Coghill; Stephanie A Smith-Warner; Dana E Rollison; Lauren R Teras; Tom K Grimsrud; Tim Waterboer Journal: Sci Rep Date: 2021-05-05 Impact factor: 4.379