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肺和脾脏中KI多瘤病毒的免疫组织化学检测

Immunohistochemical detection of KI polyomavirus in lung and spleen.

作者信息

Siebrasse Erica A, Nguyen Nang L, Smith Colin, Simmonds Peter, Wang David

机构信息

Washington University School of Medicine, Campus Box 8230, 660 S. Euclid Ave., St. Louis, MO 63110, USA.

Department of Pathology, University of Edinburgh, Scotland, UK.

出版信息

Virology. 2014 Nov;468-470:178-184. doi: 10.1016/j.virol.2014.08.005. Epub 2014 Sep 3.

Abstract

Little is known about the tissue tropism of KI polyomavirus (KIPyV), and there are no studies to date describing any specific cell types it infects. The limited knowledge of KIPyV tropism has hindered study of this virus and understanding of its potential pathogenesis in humans. We describe tissues from two immunocompromised patients that stained positive for KIPyV antigen using a newly developed immunohistochemical assay targeting the KIPyV VP1 (KVP1) capsid protein. In the first patient, a pediatric bone marrow transplant recipient, KVP1 was detected in lung tissue. Double immunohistochemical staining demonstrated that approximately 50% of the KVP1-positive cells were CD68-positive cells of the macrophage/monocyte lineage. In the second case, an HIV-positive patient, KVP1 was detected in spleen and lung tissues. These results provide the first identification of a specific cell type in which KVP1 can be detected and expand our understanding of basic properties and in vivo tropism of KIPyV.

摘要

人们对KI多瘤病毒(KIPyV)的组织嗜性知之甚少,迄今为止也没有研究描述它感染的任何特定细胞类型。对KIPyV嗜性的有限了解阻碍了对该病毒的研究及其在人类中潜在发病机制的理解。我们描述了两名免疫功能低下患者的组织,使用一种新开发的针对KIPyV VP1(KVP1)衣壳蛋白的免疫组织化学检测方法,这些组织对KIPyV抗原呈阳性染色。在第一名患者中,一名儿科骨髓移植受者,在肺组织中检测到KVP1。双重免疫组织化学染色表明,约50%的KVP1阳性细胞是巨噬细胞/单核细胞谱系的CD68阳性细胞。在第二个病例中,一名HIV阳性患者,在脾脏和肺组织中检测到KVP1。这些结果首次鉴定出了可检测到KVP1的特定细胞类型,并扩展了我们对KIPyV基本特性和体内嗜性的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e356/4254350/4e18f939a12f/nihms622619f1.jpg

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Immunohistochemical detection of KI polyomavirus in lung and spleen.肺和脾脏中KI多瘤病毒的免疫组织化学检测
Virology. 2014 Nov;468-470:178-184. doi: 10.1016/j.virol.2014.08.005. Epub 2014 Sep 3.

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