No detection of parvovirus B19 or herpesvirus DNA in giant cell arteritis

被引:42
作者
Rodriguez-Pla, A
Bosch-Gil, JA
Echevarria-Mayo, JE
Rossello-Urgell, J
Solans-Laque, R
Huguet-Redecilla, P
Stone, JH
Vilardell-Tarres, M
机构
[1] Johns Hopkins Univ, Dept Pediat, Stanley Div Dev Neurovirol, Baltimore, MD 21287 USA
[2] Univ Barcelona, Hosp Gen Valle Hebron, Dept Internal Med, Barcelona 08035, Spain
[3] Inst Salud Carlos III, Natl Ctr Microbiol, Serv Diagnost Microbiol, Madrid 28220, Spain
[4] Univ Barcelona, Hosp Gen Valle Hebron, Dept Prevent Med & Epidemiol, Barcelona 08035, Spain
[5] Univ Barcelona, Hosp Gen Valle Hebron, Dept Pathol, Barcelona 08035, Spain
[6] Johns Hopkins Univ, Sch Med, Johns Hopkins Vasculitis Ctr, Baltimore, MD USA
关键词
giant cell arteritis; infectious agents; parvovirus; herpesviruses; pathogenesis;
D O I
10.1016/j.jcv.2004.05.003
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Background: Compelling arguments exist for a role of infectious agent in giant cell arteritis (GCA). Parvovirus B 19 and several herpesviruses have focussed the attention in recent years, but the few studies to date have yielded inconsistent results. Objectives: To study the relationship between the presence of parvovirus B 19 DNA or major known herpesviruses and the histopathological features of GCA. Study design: Between January 1997 and March 2002, 147 consecutive temporal artery biopsies were performed in our center because of a clinical suspicion of GCA. Using polymerase chain reaction (PCR) procedures validated by the World Health Organization and employed routinely by our laboratory, we examined the paraffin-embedded specimens for DNA from parvovirus B 19, herpes simplex viruses (HSV) I and 2, Epstein-Barr virus (EBV), varicella-zoster virus (VZV), human cytomegalovirus (HCMV), and human herpesvirus 6 (HHV-6). We investigated positive results further with immunohistochemistry studies. Results: Fifty of the 147 temporal artery biopsies (34%) showed histological features of GCA. Three biopsies (2.5%) were initially PCR positive for parvovirus B19. None of the herpesvirus PCR assays were positive. Upon repeat testing by both PCR and immunohistochemistry, none of the three initially positive parvovirus B 19 assays were confirmed. The results of both positive and negative control assays in these studies validated these findings. We confirmed the presence of amplifiable DNA in the temporal artery biopsy specimens using PCR primers for beta-globin and indoleamine 2,3-dioxygenase (IDO). Conclusions: The results of our study do not support a role in the etiopathogenesis of GCA for either parvovirus B 19 or any of these six herpesviruses. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:11 / 15
页数:5
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