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Characterization of Humoral Immune Responses Against Capsid Protein P24 and Transmembrane Glycoprotein Gp41 of Human Immunodeficiency Virus Type 1 in China

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Journal PLoS One
Date 2016 Nov 2
PMID 27802337
Citations 2
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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.

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References
1.
Liu G, Wang J, Xiao J, Zhao Z, Zheng Y . Preparation and characterization of three monoclonal antibodies against HIV-1 p24 capsid protein. Cell Mol Immunol. 2007; 4(3):203-8. View

2.
Wu J, Patterson-Lomba O, Novitsky V, Pagano M . A Generalized Entropy Measure of Within-Host Viral Diversity for Identifying Recent HIV-1 Infections. Medicine (Baltimore). 2015; 94(42):e1865. PMC: 4620842. DOI: 10.1097/MD.0000000000001865. View

3.
Longosz A, Serwadda D, Nalugoda F, Kigozi G, Franco V, H Gray R . Impact of HIV subtype on performance of the limiting antigen-avidity enzyme immunoassay, the bio-rad avidity assay, and the BED capture immunoassay in Rakai, Uganda. AIDS Res Hum Retroviruses. 2013; 30(4):339-44. PMC: 3976571. DOI: 10.1089/aid.2013.0169. View

4.
Serhir B, Hamel D, Doualla-Bell F, Routy J, Beaulac S, Legault M . Performance of Bio-Rad and Limiting Antigen Avidity Assays in Detecting Recent HIV Infections Using the Quebec Primary HIV-1 Infection Cohort. PLoS One. 2016; 11(5):e0156023. PMC: 4880343. DOI: 10.1371/journal.pone.0156023. View

5.
Wang N, Zhong P . [Molecular epidemiology of HIV in China: 1985-2015]. Zhonghua Liu Xing Bing Xue Za Zhi. 2015; 36(6):541-6. View