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J Virol ; 81(12): 6187-96, 2007 Jun.
Article in English | MEDLINE | ID: mdl-17409164

ABSTRACT

The study of the evolution and specificities of neutralizing antibodies during the course of human immunodeficiency virus type 1 (HIV-1) infection may be important in the discovery of possible targets for vaccine design. In this study, we assessed the autologous and heterologous neutralization responses of 14 HIV-1 subtype C-infected individuals, using envelope clones obtained within the first 2 months postinfection. Our data show that potent but relatively strain-specific neutralizing antibodies develop within 3 to 12 months of HIV-1 infection. The magnitude of this response was associated with shorter V1-to-V5 envelope lengths and fewer glycosylation sites, particularly in the V1-V2 region. Anti-MPER antibodies were detected in 4 of 14 individuals within a year of infection, while antibodies to CD4-induced (CD4i) epitopes developed to high titers in 12 participants, in most cases before the development of autologous neutralizing antibodies. However, neither anti-MPER nor anti-CD4i antibody specificity conferred neutralization breadth. These data provide insights into the kinetics, potency, breadth, and epitope specificity of neutralizing antibody responses in acute HIV-1 subtype C infection.


Subject(s)
HIV Infections/immunology , HIV Infections/virology , HIV-1/metabolism , Acute Disease , Amino Acid Sequence , Antibody Formation , CD4-Positive T-Lymphocytes/immunology , Cloning, Molecular , Epitopes/chemistry , Female , Glycosylation , HIV-2/metabolism , Humans , Molecular Sequence Data , Neutralization Tests , Sequence Homology, Amino Acid
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