Merkel Cell Polyomavirus Infection in HIV-Positive Men

被引:39
|
作者
Wieland, Ulrike [2 ]
Silling, Steffi [2 ]
Scola, Nina [1 ]
Potthoff, Anja [1 ]
Gambichler, Thilo [1 ]
Brockmeyer, Norbert H. [1 ]
Pfister, Herbert [2 ]
Kreuter, Alexander [1 ]
机构
[1] Ruhr Univ Bochum, Dept Dermatol Venereol & Allergol, D-44791 Bochum, Germany
[2] Univ Cologne, Inst Virol, Natl Reference Ctr Papillomaviruses & Polyomaviru, Cologne, Germany
关键词
HUMAN-PAPILLOMAVIRUS DNA; NONMELANOMA SKIN-CANCER; RESPIRATORY-TRACT; UNITED-STATES; CARCINOMA; VIRUS; TRANSMISSION; INDIVIDUALS; EXPRESSION; TISSUES;
D O I
10.1001/archdermatol.2011.42
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Objective: To evaluate Merkel cell polyomavirus (MCPyV) DNA prevalence and load among men with human immunodeficiency virus (HIV) (hereafter referred to as HIV-positive men) and among healthy male control subjects. Design: Prospective study from February 4, 2009, through April 24, 2010. Setting: Dermatology department of a university hospital. Patients: A total of 449 male adults were prospectively recruited, including 210 HIV-positive men who have sex with men and 239 healthy controls. Cutaneous swabs were obtained once from the surface of the forehead in all participants. Main Outcome Measures: Swabs were evaluated for the presence of MCPyV DNA using single-round and nested polymerase chain reaction. The MCPyV DNA load (the number of MCPyV DNA copies per beta-globin gene copy) was determined in MCPyV-positive samples using quantitative real-time polymerase chain reaction. Results: Among 449 forehead swabs analyzed, MCPyV DNA was detected in 242 (53.9%). Compared with healthy controls, HIV-positive men more frequently had MCPyV DNA on nested polymerase chain reaction (49.4% vs 59.0%, P=.046) and on single-round polymerase chain reaction (15.9% vs 28.1%, P=.002). The MCPyV DNA loads in HIV-positive men were similar to those in HIV-negative men, but HIV-positive men with poorly controlled HIV infection had significantly higher MCPyV DNA loads than those who had well-controlled HIV infection (median and mean MCPyV DNA loads, 2.48 and 273.04 vs 0.48 and 11.84; P=.046). Conclusions: Cutaneous MCPyV prevalence is increased among HIV-positive men who have sex with men. Furthermore, MCPyV DNA loads are significantly higher in HIV-positive men with poorly controlled HIV infection compared with those who have well-controlled HIV infection. This could explain the increased risk of MCPyV-associated Merkel cell carcinoma observed among HIV-positive individuals. Arch Dermatol. 2011; 147(4): 401-406
引用
收藏
页码:401 / 406
页数:6
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