Important note: Information in this article was accurate in 1996. The state of the art may have changed since the publication date.
Cross-linking of Fc gamma receptors activates HIV-1 long terminal repeat-driven transcription in human monocytes.
Int Immunol. 1995 Oct;7(10):1665-70. Unique Identifier : AIDSLINE MED/96128660 Tsitsikov EN; Fuleihan R; McIntosh K; Scholl PR; Geha RS; Division of Immunology, Children's Hospital, Boston, MA 02115,; USA.
Abstract:
Elevation of the levels of circulating immune complexes frequently accompanies HIV-1 infection and is a prognostic indicator of clinical progression from asymptomatic infection to AIDS. Here we report that cross-linking of Fc gamma RI or Fc gamma RII by adherent human IgG or by specific anti-Fc gamma R mAb activates HIV-1 gene expression in the human monocytic cell line BF24 and increased HIV RNA expression in monocytes from HIV infected patients as assayed by reverse transcription-PCR. In THP-1 cells, Fc gamma R cross-linking induced NF-kappa B, which is known to bind to the regulatory region of the long terminal repeat (LTR) of HIV-1 and to activate HIV-1 transcription. Anti-TNF-alpha antibody but not anti-IL-1 beta antibody strongly inhibited both the induction of HIV-1-LTR-driven transcription and the induction of NF-kappa B by Fc gamma R cross-linking. These results indicate that Fc gamma R can mediate a TNF-alpha-dependent induction of HIV-1 gene transcription and suggest that immune complexes may contribute to the pathophysiology of HIV-1 infection by augmenting viral replication in monocytes.
Keywords: Acquired Immunodeficiency Syndrome/*BLOOD/IMMUNOLOGY/VIROLOGY Antibodies, Monoclonal/IMMUNOLOGY Antigen-Antibody Complex/*IMMUNOLOGY Base Sequence Chloramphenicol Acetyltransferase/BIOSYNTHESIS/GENETICS *Gene Expression Regulation, Viral Genes, Reporter Human *HIV Long Terminal Repeat HIV-1/GENETICS/PHYSIOLOGY IgG/*IMMUNOLOGY Immunoglobulins, Fab/IMMUNOLOGY *Immunologic Capping Leukemia, Monocytic, Acute/PATHOLOGY Molecular Sequence Data Monocytes/*IMMUNOLOGY/VIROLOGY NF-kappa B/METABOLISM Receptors, IgG/*IMMUNOLOGY Recombinant Fusion Proteins/BIOSYNTHESIS RNA, Viral/BIOSYNTHESIS/GENETICS Support, Non-U.S. Gov't Support, U.S. Gov't, P.H.S. *Transcription, Genetic Tumor Cells, Cultured Tumor Necrosis Factor/PHYSIOLOGY JOURNAL ARTICLE 960530
M9650837
AEGiS presents published material, reprinted with permission and neither endorses nor opposes any material. All information contained on this website, including information relating to health conditions, products, and treatments, is for informational purposes only. It is often presented in summary or aggregate form. It is not meant to be a substitute for the advice provided by your own physician or other medical professionals. Always discuss treatment options with a doctor who specializes in treating HIV.