中华皮肤科杂志 ›› 2008, Vol. 41 ›› Issue (11): 732-735.

• 论著 • 上一篇    下一篇

人类疱疹病毒8型ORF26基因亚型与Kaposi肉瘤的相关性研究

吴秀娟 普雄明 吴卫东   

  1. 新疆维吾尔自治区人民医院皮肤性病科
  • 收稿日期:2007-12-25 修回日期:2008-02-01 发布日期:2008-11-15
  • 通讯作者: 吴秀娟 E-mail:wxj7795@163.com

Relationship between open reading frame 26 subtypes in human herpesvirus-8 and Kaposi′s sarcoma

吴秀娟 Wu Xiu-juan   

  • Received:2007-12-25 Revised:2008-02-01 Published:2008-11-15
  • Contact: 吴秀娟 Wu Xiu-juan E-mail:wxj7795@163.com

摘要: 目的 明确Kaposi肉瘤患者感染的人类疱疹病毒8型(HHV-8)ORF26基因亚型分类,初步探讨其与Kaposi肉瘤不同临床分型及侵袭性的相关性。方法 对32例Kaposi肉瘤石蜡包埋组织进行HHV-8 DNA抽提、扩增、双向测序,使用DNAStar软件、Clustal W软件和PHYLIP软件包对测序结果进行系统发生学分析,从而确定HHV-8 ORF26基因亚型,最后运用Fisher确切概率法对结果进行统计学分析。结果 32例Kaposi肉瘤中有30例HHV-8阳性,阳性率为93.75%,其中6例艾滋病相关型患者HHV-8均阳性。30例HHV-8阳性患者中,17例为HHV-8 ORF26 A亚型,13例为C亚型。不同亚型间Kaposi肉瘤患者有无黏膜损害及临床分型的分布差异均无统计学意义(P > 0.05)。结论 Kaposi肉瘤患者感染HHV-8 ORF26亚型属于A亚型和C亚型,不同亚型与黏膜损害及临床分型无关。

关键词: 肉瘤, 卡波西;疱疹病毒8型,

Abstract: Objective To learn the subtypes of open reading frame 26 (ORF26) of human herpesvirus 8 (HHV-8) in patients with Kaposi′s sarcoma, and to evaluate the relationship of ORF26 subtypes to clinical types and invasiveness of Kaposi′s sarcoma. Methods Thirty-two paraffin-embeded tissue specimens of Kaposi′s sarcoma were collected in the Department of Dermatology, People′s Hospital of Xinjiang Uygur Autonomous Region, from 1996 to 2007. DNA was extracted from these specimens, nested-PCR was used to amplify HHV-8 DNA. PCR products were subjected to bi-directional sequencing after extraction from agarose gels. Phylogenetic analysis was carried out by using the software DNAStar, program Clustal W and PHYLIP package for the determination of ORF26 subtype. Fisher′s exact test was performed to evaluate the relationship of ORF26 subtypes to clinical types and invasiveness of Kaposi′s sarcoma. Results Of the 32 specimens, 30 were positive for HHV-8 DNA with a positivity rate of 93.75%, and 6 specimens of AIDS related Kaposi′s sarcoma were all positive. ORF26 A subtype was detected in the HHV-8 DNA of 17 positive specimens, and C subtype in that of other 13 specimens. Neither the incidence of mucosal lesions nor the distribution of clinical subtypes was of significant difference between patients with ORF26 A subtype and those with ORF26 C subtype (both P > 0.05). Conclusions A and C may be the predominate subtypes of ORF 26 in HHV-8 of patients with Kaposi′s sarcoma, and the ORF26 subtype is unrelated to the presence of mucosal lesions in or the clinical types of patients with Kaposi′s sarcoma.