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Lymphotropism of Merkel Cell Polyomavirus Infection, Nova Scotia, Canada

机译:加拿大新斯科舍省默克尔细胞多瘤病毒感染的淋巴性

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To test the hypothesis that Merkel cell polyomavirus (MCPyV) can infect cells of the lymphoid system, we ana-lyzed 353 specimens, including 152 non-Hodgkin lympho-mas, 44 Hodgkin lymphomas, 110 benign lymph nodes, 27 lymph nodes with metastasis, and 20 extranodal tis-sue 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 nor-mal lymph nodes. Other samples were MCPyV negative. Sequence analysis of 9 virus-positive samples confi rmed the identity of MCPyV; 3 viral strains were represented. Im-munohistochemical testing showed that 1 T-cell lymphoma expressed MCPyV T-antigen. These fi ndings suggest that the lymphoid system plays a role in MCPyV infection and may be a site for MCPyV persistence
机译:为了检验默克尔细胞多瘤病毒(MCPyV)可以感染淋巴系统细胞的假设,我们分析了353个标本,包括152个非霍奇金淋巴瘤,44个霍奇金淋巴瘤,110个良性淋巴结,27个有转移的淋巴结,和20个结外组织样本。通过定量PCR在196个淋巴瘤中的13个(6.6%)中检测到MCPyV DNA,包括24个慢性淋巴细胞性白血病标本中的5个(20.8%),在110个良性淋巴结中,有11个(10%)检测到MCPyV DNA,其中8个(13.1%)反应性增生的61个样品和29个正常淋巴结中的3个(10.3%)。其他样品均为MCPyV阴性。对9个病毒阳性样品的序列分析证实了MCPyV的身份。代表了3种病毒株。免疫组织化学测试显示1个T细胞淋巴瘤表达MCPyV T抗原。这些发现表明,淋巴系统在MCPyV感染中起作用,并且可能是MCPyV持久性的部位

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