Detection of Herpes Simplex Virus DNA in Cutaneous Lesions of Erythema Multiforme

• Published in: Journal of investigative dermatology Vol. 93; no. 1; pp. 183 - 187
• Main Authors: Brice, Sylvia L., Krzemien, Donna, Weston, William L., Huff, J. Clark
• Format: Journal Article
• Language: English
• Published: Danvers, MA Elsevier Inc 01-07-1989; Nature Publishing
• Subjects: Biological and medical sciences; Dermatology; DNA, Viral - metabolism; Erythema Multiforme - etiology; Erythema Multiforme - metabolism; Herpes Simplex - complications; Herpes simplex virus; Humans; Medical sciences; Nucleic Acid Hybridization; RNA Probes; Simplexvirus - genetics; Skin - metabolism; Skin involvement in other diseases. Miscellaneous. General aspects; Bullous dermatosis; Human; Skin disease; Herpesviridae; Alphaherpesvirinae; Erythema multiform; Herpes; Exploration; Infection; Virus; Viral disease; Isolation; Herpesvirus hominis
• ISSN: 0022-202X; 1523-1747
• DOI: 10.1111/1523-1747.ep12277397

The association between erythema multiforme (EM) and herpes simplex virus (HSV) infection has long been appreciated, although the exact role which HSV may play in the pathogenesis of this herpes-associated EM (HAEM), is unknown. Previous studies have suggested, but not definitively demonstrated, the presence of HSV in lesions of HAEM. The presence of HSV would support the hypothesis that an immune-mediated response directed against HSV-specific antigens in the skin is central to lesion development in HAEM. The purpose of this study was to examine lesions of EM for the presence of HSV DNA by using the polymerase chain reaction (PCR). In addition, in situ hybridization using an HSV-specific RNA probe was performed to further localize the HSV nucleic acids within the skin. DNA was extracted from formalin-fixed, paraffin-embedded specimens of cutaneous lesions of HAEM and also from EM for which no precipitating factor could be documented, otherwise known as idiopathic EM (IPEM). DNA from lesions of bullous pemphigoid served as a negative control. Using PCR to specifically amplify HSV suquences which might be present, and then performing Southern analysis, we demonstrated HSV DNA in9/13 HAEM and 6/9 IPEM biopsies. No HSV was detected in six lesions of bullous pemphigoid. In situ hybridization of three cutaneous HAEM lesions using an 35S-labeled HSV-specific RNA probe localized the HSV nucleic acids predominantly to the epidermis. Three biopsies of chronic dermatitis used as negative controls, did not demonstrate this specific hybridization. These finding confirm the presence of HSV in lesions of HAEM and are consistent with the concept of an HSV-specific immune-mediated pathogenesis for this disease. In addition, most cases of IPEM appear to be herpes associated despite the absence of clinically apparent HSV infection.