In vitro infection of human monocytes with human T lymphotropic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV)

• Published in: The Journal of immunology (1950) Vol. 137; no. 1; pp. 323 - 329
• Main Authors: Nicholson, JK, Cross, GD, Callaway, CS, McDougal, JS
• Format: Journal Article
• Language: English
• Published: Bethesda, MD Am Assoc Immnol 01.07.1986; American Association of Immunologists
• Subjects: AIDS/HIV; Antibodies, Monoclonal - physiology; Binding Sites, Antibody; Binding, Competitive; Biological and medical sciences; Deltaretrovirus - immunology; Deltaretrovirus - metabolism; Fundamental and applied biological sciences. Psychology; Humans; Microbiology; Monocytes - metabolism; Monocytes - microbiology; Monocytes - ultrastructure; Replicative cycle, interference, host-virus relations, pathogenicity, miscellaneous strains; Retroviridae Infections - microbiology; Retroviridae Infections - transmission; T-Lymphocytes - immunology; T-Lymphocytes - metabolism; T-Lymphocytes - microbiology; Virology; Virus Replication; Human; Cell culture; Monocyte; Antibody; Retroviridae; Molecular interaction; Reservoir; HTLV-III virus; Cell surface; Virus; Transmission electron microscopy; Infectivity; Target cell; Inhibition; Permissiveness; LAV virus
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.137.1.323

We explored the possibility that normal human monocytes can be infected with the retrovirus human T lymphotropic virus type III/lymphadenopathy-associated virus (HTLV-III/LAV). The T4 antigen, believed to be the receptor for HTLV-III/LAV binding to CD4 cells, is found on monocytes at low levels. Anti-T4A, which recognizes an epitope on the T4 molecule, inhibits viral binding to monocytes, and virus inhibits anti-T4A binding, although inhibition in both cases is not total. Virus particles were detected in HTLV-III/LAV-pulsed monocytes by electron microscopy as early as 10 min and for up to 3 days after inoculation, although budding virus was not observed. Monocytes were exposed to virus, were washed, and were cultured. Monocyte cultures were monitored by conventional assays for virus replication: immunofluorescence detection of cytoplasmic virus, supernatant reverse transcriptase activity, and supernatant virus antigen. These assays were either negative or at the lower limits of positivity. However, the amount of infectious virus was shown to increase over time in monocyte cultures by harvesting monocytes or their culture supernatants and titrating them into assay cultures containing stimulated T cells. Virus recovery from monocytes and virus recovery from T cells differed both quantitatively and qualitatively. Recovery from T cells and T cell supernatants peaked at 3 to 6 days and declined thereafter. Recovery from monocytes and monocyte supernatants increased over time in culture and never attained the levels of T cell cultures. Taken together, these studies indicate that HTLV-III/LAV binds to monocytes via the T4 molecule and enters the cells. Infectious virus is retained and increases with time in infected monocyte cultures. Both viral binding and infection are at low levels compared with levels in T cells. Unlike the usual infection of T cells characterized by high level virus replication with cell depletion, the infection appears to be persistent in monocytes.