Factor I-Mediated Processing of Complement Fragments on HIV Immune Complexes Targets HIV to CR2-Expressing B Cells and Facilitates B Cell-Mediated Transmission of Opsonized HIV to T Cells

Our study demonstrates that binding of complement-opsonized HIV to complement receptor type 1 on human erythrocytes (E) via C3b fragments is followed by a rapid normal human serum-mediated detachment of HIV from E. The release was dependent on the presence of factor I indicating a conversion of C3b...

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Veröffentlicht in:Journal of Immunology 2006-09, Vol.177 (5), p.3469-3476
Hauptverfasser: Banki, Zoltan, Wilflingseder, Doris, Ammann, Christoph G, Pruenster, Monika, Mullauer, Brigitte, Hollander, Karoline, Meyer, Martina, Sprinzl, Georg M, van Lunzen, Jan, Stellbrink, Hans-Jurgen, Dierich, Manfred P, Stoiber, Heribert
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container_end_page 3476
container_issue 5
container_start_page 3469
container_title Journal of Immunology
container_volume 177
creator Banki, Zoltan
Wilflingseder, Doris
Ammann, Christoph G
Pruenster, Monika
Mullauer, Brigitte
Hollander, Karoline
Meyer, Martina
Sprinzl, Georg M
van Lunzen, Jan
Stellbrink, Hans-Jurgen
Dierich, Manfred P
Stoiber, Heribert
description Our study demonstrates that binding of complement-opsonized HIV to complement receptor type 1 on human erythrocytes (E) via C3b fragments is followed by a rapid normal human serum-mediated detachment of HIV from E. The release was dependent on the presence of factor I indicating a conversion of C3b fragments to iC3b and C3d on the viral surface. This in turn resulted in an efficient binding of opsonized HIV to CR2-expressing B cells, thus facilitating B cell-mediated transmission of HIV to T cells. These data provide a new dynamic view of complement opsonization of HIV, suggesting that association of virus with E might be a transient phenomenon and the factor I-mediated processing of C3b to iC3b and C3d on HIV targets the virus to complement receptor type 2-expressing cells. Thus, factor I in concert with CR1 on E and factor H in serum due to their cofactor activity are likely to be important contributors for the generation of C3d-opsonized infectious HIV reservoirs on follicular dendritic cells and/or B cells in HIV-infected individuals.
doi_str_mv 10.4049/jimmunol.177.5.3469
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subjects B-Lymphocytes - immunology
B-Lymphocytes - metabolism
B-Lymphocytes - virology
Complement System Proteins - chemistry
Complement System Proteins - immunology
Complement System Proteins - metabolism
Fibrinogen - metabolism
HIV - immunology
HIV Infections - immunology
HIV Infections - virology
Human immunodeficiency virus
Humans
Kinetics
Receptors, Complement 3d - immunology
Serum
T-Lymphocytes - immunology
T-Lymphocytes - virology
title Factor I-Mediated Processing of Complement Fragments on HIV Immune Complexes Targets HIV to CR2-Expressing B Cells and Facilitates B Cell-Mediated Transmission of Opsonized HIV to T Cells
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