Characterization of Humoral Immune Responses against Capsid Protein p24 and Transmembrane Glycoprotein gp41 of Human Immunodeficiency Virus Type 1 in China

PLoS One. 2016 Nov 1;11(11):e0165874. doi: 10.1371/journal.pone.0165874. eCollection 2016.

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.

MeSH terms

  • Antibodies, Viral / blood
  • Antibodies, Viral / immunology
  • China
  • Cross-Sectional Studies
  • HIV Core Protein p24 / immunology*
  • HIV Envelope Protein gp41 / immunology*
  • HIV-1 / immunology*
  • Humans
  • Immunity, Humoral*
  • Longitudinal Studies

Substances

  • Antibodies, Viral
  • HIV Core Protein p24
  • HIV Envelope Protein gp41

Grants and funding

This research is supported by Guangzhou Science and Technology Program sponsored by Bureau of Science and Information Technology of Guangzhou Municipality (no. 201508020018). This research is also supported by Guangdong Province Public Welfare Research and Capacity Building Project sponsored by Guangdong Provincial Department of Science and Technology (no. 2014B020212007). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.