HUMAN CYTOMEGALOVIRUS AS A POTENTIAL ETIOLOGIC AGENT IN RECURRENT APHTHOUS ULCERS AND BEHCETS-DISEASE

Citation
A. Sun et al., HUMAN CYTOMEGALOVIRUS AS A POTENTIAL ETIOLOGIC AGENT IN RECURRENT APHTHOUS ULCERS AND BEHCETS-DISEASE, Journal of oral pathology & medicine, 25(5), 1996, pp. 212-218
Citations number
42
Categorie Soggetti
Dentistry,Oral Surgery & Medicine",Pathology
ISSN journal
09042512
Volume
25
Issue
5
Year of publication
1996
Pages
212 - 218
Database
ISI
SICI code
0904-2512(1996)25:5<212:HCAAPE>2.0.ZU;2-V
Abstract
In a preliminary study on anti-human cytomegalovirus (HCMV) antibody ( Ab) by ELISA, the serum anti-HCMV/IgG Ab concentrations in 22 patients with recurrent aphthous ulcers (RAU) in the remission stage were foun d to be significantly higher than in 22 control subjects (121+/-42 vs 100+/-27, P<0.05) and in 39 patients with RAU in the active stage (121 +/-42 vs 88+/-45, P<0.01). Therefore, the potential of HCMV as an etio logic agent in RAU was proposed and studies using the polymerase chain reaction (PCR) and in situ hybridization (ISH) have been performed to investigate the possible presence of HCMV DNA in pre-ulcerative oral aphthous lesions in patients with RAU or Behcet's disease (BD) of the mucocutaneous type. For this purpose, formalin-fixed biopsy specimens were obtained from 13 pre-ulcerative oral aphthous lesions, 2 samples of normal oral mucosa and 1 ileal mucosal lesion from 9 RAU patients a nd 4 BD patients. Five specimens of normal oral mucosa from 5 normal c ontrol subjects and 12 specimens of oral erosive or ulcerative lesions from 12 patients with erosive lichen planus (ELP) were also included. By PCR, HCMV DNA was detected in 5 of the 13 (38.5%) pre-ulcerative o ral aphthous lesions, 3 from RAU patients and 2 from BD patients. The ileal mucosa specimen was also HCMV DNA-positive, whereas HCMV DNA was not demonstrated in any of the 7 specimens of normal oral mucosa from RAU patients and normal control subjects; 12 specimens of oral lesion s from ELP patients were similarly negative. ISH did not detect HCMV D NA in any of the biopsy specimens from RAU patients and control subjec ts. Our findings suggest that HCMV may be an etiologic agent in some c ases of RAU and BD.