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PMID: 12164651 Published · ppublish English Journal Article Review

Mechanisms of expression of HHV8, EBV and HPV in selected HIV-associated oral lesions.

Oral diseases ·Vol. 8 Suppl 2 ·2002-00-00 ·Pages 161-8

Hille JJ, Webster-Cyriaque J, Palefski JM, Raab-Traub N

Abstract

Opportunistic DNA viruses, particularly members of the herpesvirus family, are frequently the aetiological agents of HIV-associated oral lesions. Oral lesions common to the early phase of the AIDS epidemic, including Kaposi's sarcoma (KS), oral aphthous ulceration, AIDS-associated oral lymphoma, and oral hairy leukoplakia (OHL), have been tested for the prevalence of Epstein-Barr virus (EBV) and Kaposi's sarcoma-associated herpesvirus (KSHV). While EBV DNA is detected by PCR in all of these lesions, abundant viral replication can only be detected in OHL. In OHL, a novel state of EBV infection has been discovered with concurrent expression of replicative and transforming proteins, with all of these proteins contributing to the development of the lesion. Activation of signalling pathways and up-regulation of the viral receptor, proliferative and antiapoptotic genes by these proteins induce several of the histological features common to OHL, such as acanthosis and hyperproliferation. In contrast to other permissive herpesvirus infections, expression of EBV transforming proteins within the permissively infected OHL tissue enables epithelial cell survival and may enhance viral replication. Detection of KSHV in these HIV-infected individuals has been localized only to their saliva. Replicative and latent KSHV gene products have been detected in association with the development of oral KS lesions. EBV, but not human cytomegalovirus (HCMV), has been detected by PCR in minor salivary gland biopsies of HIV-associated salivary gland disease. Human papillomaviruses (HPV) are associated with oral warts in HIV-positive individuals; a diagnosis that appears to be increasing in frequency in the era of highly active antiretroviral therapy. To date, there appears to be little increase in the incidence of HPV-associated oral cancer. The mechanisms of interaction between HIV and HPV are not fully understood. Expression of viral gene products is clearly important and necessary for the development of multiple AIDS-associated oral lesions.

MeSH Terms
AIDS-Related Opportunistic Infections/virology Apoptosis/physiology Basic-Leucine Zipper Transcription Factors Carrier Proteins/analysis Cell Division/physiology Cell Survival Cytomegalovirus/physiology Cytomegalovirus Infections/complications Epithelial Cells/virology Epstein-Barr Virus Infections/complications HIV Infections/complications Herpesvirus 4, Human/physiology Herpesvirus 8, Human/physiology Humans Leukoplakia, Hairy/virology Lymphoma, AIDS-Related/virology Mouth Diseases/virology Mouth Mucosa/virology Mouth Neoplasms/virology Oncogene Proteins, Viral/analysis Papillomaviridae/physiology Papillomavirus Infections/complications Receptors, Virus/physiology Repressor Proteins Saliva/virology Salivary Gland Diseases/virology Sarcoma, Kaposi/virology Signal Transduction/physiology Stomatitis, Aphthous/virology Up-Regulation/physiology Viral Proteins/analysis Virus Replication Warts/virology
Chemicals
Basic-Leucine Zipper Transcription Factors Carrier Proteins K8 protein, Human herpesvirus 8 Oncogene Proteins, Viral Receptors, Virus Repressor Proteins Viral Proteins
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Hille J J
Department of Oral & Maxillofacial Pathology, University of the Western Cape, Cape Town, South Africa. uwcwho@iafrica.com
Webster-Cyriaque J
Palefski J M
Raab-Traub N
Article Info
Journal
Oral diseases
Abbr.
Oral Dis
ISSN
1354-523X
Published
2002-00-00
Pages
161-8
Language
English
Region
Denmark
NLM ID
9508565
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