Analysis of the HIV-1 gp41 specific immune response using a multiplexed antibody detection assay

A fluorescence-based, multiplexed, antibody-binding and mapping assay was developed to characterize antibody responses in HIV-1-infected individuals to the ectodomain of the HIV-1 gp41 envelope glycoprotein. The antigen panel included intact recombinant gp41, the fusion peptide region, the polar reg...

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Veröffentlicht in:Journal of immunological methods 2004-04, Vol.287 (1), p.49-65
Hauptverfasser: Opalka, David, Pessi, Antonello, Bianchi, Elisabetta, Ciliberto, Gennaro, Schleif, William, McElhaugh, Michael, Danzeisen, Renee, Geleziunas, Romas, Miller, Michael, Eckert, Debra M., Bramhill, David, Joyce, Joseph, Cook, James, Magilton, William, Shiver, John, Emini, Emilio, Esser, Mark T.
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Sprache:eng
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Zusammenfassung:A fluorescence-based, multiplexed, antibody-binding and mapping assay was developed to characterize antibody responses in HIV-1-infected individuals to the ectodomain of the HIV-1 gp41 envelope glycoprotein. The antigen panel included intact recombinant gp41, the fusion peptide region, the polar region, the N-heptad region, the C-heptad region as well as overlapping epitopes in the 2F5 and 4E10 monoclonal antibody-binding regions. The panel included both native and constrained peptides specifically designed to mimic putative gp41 prefusion and fusion intermediates. The results of these analyses revealed a broad pattern of immune responses against the test antigens, suggesting that none of these gp41 regions are immunologically silent. The HIV-1-positive sera were also evaluated using infectivity inhibition assays. No correlation was evident between the breadth or magnitude of specific anti-gp41 reactivities and virus neutralization potency. These evaluations demonstrated the substantial potential of the multiplexed antibody binding and mapping assay for rapid and sensitive analysis of complex antibody responses.
ISSN:0022-1759
1872-7905
DOI:10.1016/j.jim.2004.01.016