Concise Review: The Anti-HIV-1 Activity Associated with Saliva
- 1 February 1997
- journal article
- Published by SAGE Publications in Journal of Dental Research
- Vol. 76 (2), 634-640
- https://doi.org/10.1177/00220345970760020301
Abstract
This review summarizes the data on the anti-human immunodeficiency virus (HIV) activity associated with saliva and the possible routes of oral transmission of HIV. Saliva can be passed from an HIV-infected individual to an uninfected person via sexual or non-sexual activities. The relative risk of HIV transmission through saliva is a subject of continuing concern for dental practitioners. HIV-infected individuals frequently have oral lesions that can cause bleeding and release of the virus into the oral cavity. In addition, viral p24 and HIV-1 RNA were detected in tonsils and adenoids even in asymptomatic seropositive individuals. Nevertheless, the potential HIV-infectivity of saliva is low, although both infectious HIV-1 and HIV DNA have been detected in saliva. This observation has led to the suggestion that saliva may contain factors that inhibit HIV-1 infectivity. At least two anti-HIV activities have been partially characterized: (i) physical entrapment of HIV by high-molecular-weight molecules (e.g., mucins), and (ii) inhibition of viral infection by soluble proteins. Several studies have indicated that, of the salivary proteins evaluated, recombinant secretory leukocyte protease inhibitor (rSLPI) could inhibit HIV-1 infection in macrophages at physiological concentrations. The anti-HIV activity of the serine protease inhibitor rSLPI is most likely due to its interaction with a cell-surface molecule(s) other than the primary HIV-1 receptor, CD4, and may involve (i) inhibition of cell-surface serine protease(s), and/or (ii) interaction with other human-specific co-factors essential for viral entry.Keywords
This publication has 78 references indexed in Scilit:
- T‐cell Membrane‐Associated Serine Protease, Tryptase TL2, Binds Human Immunodeficiency Virus Type 1 gp120 and Cleaves the Third‐Variable‐Domain Loop of gp120European Journal of Biochemistry, 1996
- Inhibition of U‐937 membrane‐associated cathepsin G by GP 120 (IIIB) and V3 loop‐derived peptides from several strains of HIV‐1FEBS Letters, 1995
- In vitro infection of epidermal langerhans cells with human immunodeficiency virus type 1 (HTLV-IIIB isolate)Research in Virology, 1993
- Effect of Mutations in the V3 Loop of HIV-1 gp120 on Infectivity and Susceptibility to Proteolytic CleavageAIDS Research and Human Retroviruses, 1993
- A Human Lymphoid Recombinant Cell Line with Functional Human Immunodeficiency Virus Type 1 EnvelopeAIDS Research and Human Retroviruses, 1993
- Involvement of tryptase‐related cellular protease(s) in human immunodeficiency virus type 1 infectionFEBS Letters, 1989
- Tissue distribution of antileukoprotease and lysozyme in humans.Journal of Histochemistry & Cytochemistry, 1989
- Low Occupational Risk of Human Immunodeficiency Virus Infection among Dental ProfessionalsNew England Journal of Medicine, 1988
- Lack of Transmission of HTLV-III/LAV Infection to Household Contacts of Patients with AIDS or AIDS-Related Complex with Oral CandidiasisNew England Journal of Medicine, 1986
- Infrequency of Isolation of HTLV-III Virus from Saliva in AIDSNew England Journal of Medicine, 1985