Document 3233 DOCN M94A3233 TI Salivary anti-HIV activity. DT 9412 AU Nagshunmugam T; Friedman H; Davis C; Abrams W; Malamud D; U. Penn. Dent. Med. Phila. 19104. SO Int Conf AIDS. 1994 Aug 7-12;10(1):122 (abstract no. PA0108). Unique Identifier : AIDSLINE ICA10/94369342 AB OBJECTIVE: Human saliva decreases HIV-1 infectivity. Some of this inhibition requires filtration and is associated with viral aggregation. The present study describes the nature of a second type of salivary anti-HIV activity. METHODS: Submandibular saliva was collected from 15 seronegative individuals. After dialysis and lyophilization, the material was incubated with virus for 2-60 min and exposed to PHA-stimulated PBMCs for 3 hrs. Cells were washed and incubated for 7 days and the amount of virus determined by p24 ELISA. Similar experiments were carried out with HSV, HIV-2 and SIV. The effects of submandibular saliva on the binding of anti-receptor antibodies to PBMCs was used to define the site of action of the salivary inhibitor. RESULTS: Saliva obtained from several individuals displayed potent anti-HIV activity not associated with viral aggregation. Salivary inhibition is time and concentration dependent, and appears to be HIV-1 specific. Little inhibition is seen for HSV, and no inhibition of viral infectivity is seen with HIV-2 or SIV. Incubation of PBMCs with submandibular saliva at high concentration appears to block the binding of anti-receptor antibodies, but at concentrations present in the in vitro infectivity assay, no inhibition was detected. CONCLUSIONS: Human saliva appears to contain two types of anti-HIV activity. The first type only seen after filtration through a nitrocellulose filter, is associated with viral aggregation. The second type of activity does not require filtration. This latter activity appears to be specific for HIV-1, and if active in vivo, could explain the lack of oral transmission. DE Acquired Immunodeficiency Syndrome/TRANSMISSION *Antiviral Agents Cells, Cultured Comparative Study Human HIV Seronegativity HIV-1/*PHYSIOLOGY/PATHOGENICITY HIV-2/PHYSIOLOGY Lymphocytes/*MICROBIOLOGY Saliva/*PHYSIOLOGY Simplexvirus/PHYSIOLOGY Submandibular Gland/SECRETION Support, U.S. Gov't, P.H.S. SIV/PHYSIOLOGY *Virus Replication MEETING ABSTRACT SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).