Abstract

The objective of this study was to extend our previous research and to further characterize the humoral immune responses against HIV-1 p24, gp41 and the specific peptides carrying the immunodominant epitopes (IDEs) that react with human serum samples from HIV-1-infected individuals in China. We found that the majority (90.45%, 180/199) of the samples did not react with any of the three HIV-1 p24 peptides carrying IDEs, but did react with the recombinant full-length p24, suggesting that these samples tested in China were primarily directed against the conformational epitopes of HIV-1 p24. In contrast, 84.54% (164/194) of the samples reacted with at least one HIV-1 linear gp41 peptide, in particular the gp41-p1 peptide (amino acids 560–616). Both recently and long-term HIV-1-infected individuals displayed similar humoral immune responses against the recombinant gp41. However, samples from long-term HIV-1-infected subjects but not from recently infected subjects, showed a very strong reaction against the gp41-p1 peptide. The different response patterns observed for the two groups against the gp41 and the peptide gp41-p1 were statistically significant (P<0.01, Chi-square test). These results have direct relevance and importance for design of improved HIV-1 p24 detection assays and the gp41- based immunoassay that can be used to reliably distinguish recent and long-term HIV-1 infection.

Highlights

  • During the natural course of human immunodeficiency virus type one (HIV-1) infection, the antibodies recognizing HIV-1 viral proteins are the important components of host humoral immune responses

  • To improve the assay sensitivity and specificity, it was necessary to identify the major immunodominant epitopes (IDEs) of HIV-1 p24, in particular in serum samples from HIV-1-infected individuals, since most of the IDEs were previously characterized with monoclonal antibodies generated in mice

  • We have extended our previous research by investigating the utilization of major HIV-1 p24 IDEs and anti-HIV response patterns in the HIV-1-infected human subjects in China

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Summary

Introduction

During the natural course of human immunodeficiency virus type one (HIV-1) infection, the antibodies recognizing HIV-1 viral proteins are the important components of host humoral immune responses. The transmembrane portion of HIV-1 envelope protein gp is the most conservative antigen that has been widely used for detection of antiHIV antibodies [1]. Neutralizing human monoclonal antibodies (mAbs) like 2F5, 4E10 have been identified to direct to HIV-1 gp, making it the primary target for vaccine development [4, 5]. The capsid protein p24 of HIV-1 is the most abundant and highly conserved viral protein and the earliest immunological biomarker detected after HIV-1 infection [6]. The fourth generation HIV-1 immunoassay combines the detection of anti-HIV-1 and anti-HIV-2 antibodies as well as HIV-1 p24 antigen and can further shorten the window period of HIV-1 detection and increase detection sensitivity [7]

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