Guttman-Yassky Emma, Cohen Adina, Kra-Oz Zippi, Friedman-Birnbaum Rachel, Sprecher Elli, Zaltzman Neli, Friedman Eitan, Silbermann Michael, Rubin Dina, Linn Shai, Whitby Dennis, Gideoni Osnat, Pollack Shimon, Bergman Reuven, Sarid Ronit
Department of Dermatology, Rambam Medical Center, and Department of Cell Biology and Anatomy, Bruce Rappaport Faculty of Medicine, Haifa, Israel.
J Infect Dis. 2004 Jun 1;189(11):2023-6. doi: 10.1086/386308. Epub 2004 May 11.
It is widely accepted that there is a causal association between Kaposi sarcoma-associated herpesvirus (KSHV) and Kaposi sarcoma (KS). However, the majority of individuals infected with KSHV never develop KS. Here, we present a unique familial case of classic KS, in which the disease occurs in 4 siblings who have no recognized underlying immunodeficiency. We examine risk factors that could play a role in this condition, including KSHV infection, KSHV DNA load, genetic variants of KSHV, infection with additional viruses, interleukin-6-promoter polymorphism, and HLA genotype. We hypothesize that a genetic susceptibility to KS, in combination with KSHV infection, may play an important role in the presented familial case.
人们普遍认为卡波西肉瘤相关疱疹病毒(KSHV)与卡波西肉瘤(KS)之间存在因果关联。然而,大多数感染KSHV的个体从未患上KS。在此,我们报告一例独特的家族性经典KS病例,该疾病发生在4名无公认潜在免疫缺陷的兄弟姐妹身上。我们研究了可能在这种情况下起作用的危险因素,包括KSHV感染、KSHV DNA载量、KSHV的基因变异、其他病毒感染、白细胞介素-6启动子多态性和HLA基因型。我们推测,对KS的遗传易感性与KSHV感染相结合,可能在该家族病例中起重要作用。