PLoS ONE · 2011 · 77 citations · 50 references
Life SciencesImmunologyMolecular BiologyAntibody EngineeringMolecular VirologyVaccine ImmunologyAntibody CharacterizationAntibody FunctionAntibody-antigen RecognitionAntiviral ImmunityHiv Vaccine DevelopmentVaccine PlatformsAntibody-mediated Viral NeutralizationAntibody-mediated Virus NeutralizationBreadth Of Antibody ResponseFusion Intermediate StatesIntermediate FusionViral Envelope GlycoproteinsViral Envelope ProteinsViral Fusion Proteins
A component to the problem of inducing broad neutralizing HIV-1 gp41 membrane proximal external region (MPER) antibodies is the need to focus the antibody response to the transiently exposed MPER pre-hairpin intermediate neutralization epitope. Here we describe a HIV-1 envelope (Env) gp140 oligomer prime followed by MPER peptide-liposomes boost strategy for eliciting serum antibody responses in rhesus macaques that bind to a gp41 fusion intermediate protein. This Env-liposome immunization strategy induced antibodies to the 2F5 neutralizing epitope ⁶⁶⁴DKW residues, and these antibodies preferentially bound to a gp41 fusion intermediate construct as well as to MPER scaffolds stabilized in the 2F5-bound conformation. However, no serum lipid binding activity was observed nor was serum neutralizing activity for HIV-1 pseudoviruses present. Nonetheless, the Env-liposome prime-boost immunization strategy induced antibodies that recognized a gp41 fusion intermediate protein and was successful in focusing the antibody response to the desired epitope.
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Cardiolipin Polyspecific Autoreactivity in Two Broadly Neutralizing HIV-1 Antibodies
Barton F. Haynes, J. T. Fleming, E. William St. Clair et al. · Science · 2005 · 747 citations · Full text