[Final Program, International Conference on AIDS (4th: 1988: Stockholm, Sweden), Book 2]

7581 EBV IN ORAL HAIRY LEUKOPLAKIA, AN ELECTRON MICROSCOPIC IMMUNOCYTOCHEMICAL STUDY. J.S. Greenspan, V. Petersen, Y. De Souza and D. Greenspan. Oral AIDS Center, University of California, San Francisco, San Francisco, CA. Objective. To accurately localize EBV components, to study the life-cycle of EBV and develop additional methods for confirmation of its presence in oral hairy leukoplakia (HL). Methods. EM immunocytochemistry was applied to 10 paraformaldehyde-fixed biopsy specimens of tongue HL and uninvolved buccal mucosa from the same patients. Etched sections of epoxy-embedded samples were labelled in a two step reaction using monoclonal antibodies to EBV-VCA and gold colloid conjugated to goat anti-mouse IgG-Fab2 purified fragment. Results. Reaction product was localized to the capsids of virus particles within ballooning and adjoining epithelial nuclei as well as within intercellular spaces in HL lesions. Ascites fluid in place of monoclonal antibody was a negative control, as was buccal mucosa. Conclusion. EM immunocytochemistry of EBV in HL confirms light-microscope findings and offers an approach to understanding the biology of EB infection of epithelial cells. 7582 EARLY ORAL LESIONS FOUND IN COMMUNITY COHORTS: IS HAIRY LEUKOPLAKIA MORE COMMON THAN CANDIDIASIS? David W Feigal, GL Overby, D Greenspan, JS Greenspan and the UCSF Oral AIDS Epidemiology Group +. University of California, San Francisco. USA. Objective: To determine the incidence and prevalence of early oral lesions in HIV infected individuals. Method: Since January 1987, six prospective cohort studies agreed to systematically examine and record oral lesions. As part of routine physical examinations, usually at 6 month intervals, 418 lesions were observed in 1514 patients. Results: 72% of lesions were white, usually flat or corrugated predominantly hairy leukoplakia. (HL) The number of prevalent lesions (present on first exam after oral examination training) and incident lesions (absent on initial examination) is shown by cohort and compared to the Oral Medicine Clinic. HL n Prev. Incid. Candidiasis Prev. Incid. AWARE 58 SF Epi Group 241 City Clinic 287 Men's Health 771 Transf.Safety......13.7 TOTAL 1494 Oral Med Clinic 273 4 33 21 66.........5..., 5 129 138 3 16 15 24 5 63 69 0 0 0 1 0 1 7 1 14 18 Conclusions: Hairy leukoplakia, in part because of its longer duration than candidiasis, is likely to be the most often detected early oral manifestation of HIV infection. + W. Winkelstein, A Moss, GW Rutherford, C Wofsy, EA Donegan, R Chaisson Notes: 7583 ORAL HAIRY LEUKOPLAKIA Angelika A. Langford*, J Becker*, P Reichart*, H Gelderblom**, X Zhang**, T Lning***, H Wolf# *Dept. for Oral Surgery (North), Free University Berlin, **Robert Koch-Institute, Berlin, *** Inst. for Pathology, University Hamburg, # Max von Pettenkofer Institute, Munich Clinical, immunhistochemical and ultrastructural findings. 70 cases of oral hairy leukokplakia (HL), occuring in 61 homosexual men, 8 i.v. drug abusers and one hemophiliac child, were clinically examined and followed up during an average time of observation of 13.5 months. All lesions were localised on the lateral and/or ventral side of the tongue. In order to evaluate, if EBV-DNA can be found only in HL of HIV-infected patients, biopsies of HL, of uninvolved oral mucosa and of oral Kaposi sarcoma were examined. Using in situ hybridisation techniques 5/6 biopsies of HL and 2/24 biopsies of oral gingiva showed EBV-DNA. In a further in situ hybridisation all EBV-DNA positive specimens were negative for CMV-DNA as well as with the applied probes of human papilloma virus type 6, II, 13, 16 and 18. By means of immunohistochemistry (APAAP) io biopsies were examined for EBV-membrane, -core and early protein pI50. An equivalent immunostaining was noted in the upper two thirds of oral epithelia. The clinical importance of reactivation of latent EBVinfection in HIV-infected patients and the role of cytotoxic T-lymphocytes for elimination of EBV-infected cells are discussed. 7584 ULTRASTRUCTURAL FINDINGS IN CLINICALLY UNINVOLVED ORAL MUCOSA OF PATIENTS WITH HIV-INFECTION Xiaolin Zhang*, A Langford**, H Gelderblom*, P Reichart** *Robert Koch-Institute, Berlin; **Dept. for Oral Surgery (North), Free University Berlin Objective. To compare ultrastructural changes of uninvolved oral mucosa of patients infected by HIV with those observed in oral Kaposi's sarcoma (AIDS) (KS) and to discuss the pathogenesis of oral KS. Methods. Biopsies of clinically uninvolved oral mucosa of 12 patients with HIV-infection (average age 34,7 yrs; male: n=Io, female: n=2; asymptomatic: n=4, ARC: n=3, AIDS: n=5, including 2 patients with KS) were studied by EM and compared to those seen in typical AIDS related KS lesions. Results. Vascular abnormalities were found in all biopsies of the HIV-infected patients regardless of the stage of the disease. In particular, protruded swollen endothelial cells were observed. Vascular channels reduced to a slit as well as a sparseness of intercellular junctions were found. Vascular walls were often revealing gaps and slits. There was an increase in quantity of Weibel-Palade bodies within the cytoplasm. Occasionally, extravasated erythrocytes were observed. These findings were similar to those described in early and late KS lesions. Comparable changes could not be observed in oral mucosa of uninfected individuals. Conclusion. The present EM findings in uninvolved oral mucosa suggest that blood vessels during HIV-infection undergo changes which probably involve the entire vascular system. Therefore, a general principle either represented by specific angiogenic factors or viral infections serve as primers of the disregulation of vascular neogenesis. 320

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[Final Program, International Conference on AIDS (4th: 1988: Stockholm, Sweden), Book 2]
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International AIDS Society
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1988
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programs
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"[Final Program, International Conference on AIDS (4th: 1988: Stockholm, Sweden), Book 2]." In the digital collection Jon Cohen AIDS Research Collection. https://name.umdl.umich.edu/5571095.0006.002. University of Michigan Library Digital Collections. Accessed June 25, 2025.
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