Biomedical Science Letters (대한의생명과학회지)
- Volume 8 Issue 4
- /
- Pages.257-268
- /
- 2002
- /
- 1738-3226(pISSN)
- /
- 2288-7415(eISSN)
Detection of Cytomegalovirus in Atherosclerotic Aorta and Coronary Artery by In Situ Hybridization and PCR
- Eom, Yong-Bin (Division of Forensic Medicine, National Institute of Scientific Investigation) ;
- Kwon, Tae-Jung (Division of Forensic Medicine, National Institute of Scientific Investigation) ;
- Lee, Sang-Yong (Division of Forensic Medicine, National Institute of Scientific Investigation) ;
- Lee, Won-Tae (Division of Forensic Medicine, National Institute of Scientific Investigation) ;
- Kim, Jong-Bae (Department of Biomedical Laboratory Science, College of Health Science)
- Published : 2002.12.01
Abstract
Chronic infection and inflammation have recently been implicated as important etiologic agents of atherosclerosis. Several agents have been suggested as possible candidates including cytomegalovirus (CMV), herpes simplex vims type 1 (HSV-1), Epstein-Barr virus (EBV), Chlamydia pneumoniae, and Helicobacter pylori. We evaluated the relationship between cytornegalovirus infection and atherosclerosis by in situ hybridization and polymerase chain reaction (PCR). We examined 23 subjects with atherosclerosis and 10 matched control subjects without atherosclerosis. CMV was detected by in situ hybridization in 60.9% (14/23) of aorta and 42.9% (9/21) of coronary arteries in subjects with atherosclerosis. It was also detected by PCR in 65.2% (15/23) of aorta and 52.4% (11/21) of coronary arteries. CMV was detected on areas showing early or advanced atheromatous changes. Cells morphologically identical to smooth muscle cells, endothelial cells, lymphocytes, fibroblasts, and Schwann cells were positively reacted with the CMV probe. However. none of the cells to which the probe hybridized contained inclusion bodies, thus strongly suggesting that the arterial wall may be a site of CMV latency. This result Indicates that CMV may potentially play a direct or indirect role in the pathogenesis of human atherosclerosis.