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    <identifier>10.57760/sciencedb.j00217.09383</identifier>
    <datestamp>2025-09-12T11:32:38Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2025-09-12</dc:date>
  <dc:title>Development and Application of Broad-Spectrum Detection Monoclonal Antibodies Against HIV-1 P24 Antigen</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.j00217.09383</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Objective To enhance the accuracy and coverage of early HIV diagnosis, this study aimed to develop anti-p24 monoclonal antibodies with broad-spectrum recognition capability.Methods Mice were immunized subcutaneously with multi-subtype recombinant HIV-1 P24 antigens. Hybridoma technology was employed to screen and produce P24-specific mAbs. Cross-reactivity was evaluated using a double-antibody sandwich chemiluminescence immunoassay against recombinant P24 proteins and viral lysates from 10 common HIV-1 genotypes, including subtypes A, B, C, D, and CRF01_AE. The affinity of coated antibodies was measured by surface plasmon resonance (SPR). A saturation mutagenesis library targeting key antigen-binding pockets of the coated antibody was constructed. Phage display technology was used to screen the library and enrich high-affinity mutants.Results Three positive hybridoma clones stably secreting antibodies were obtained, all demonstrating strong binding activity against all 10 tested HIV-1 genotypes. The affinity-matured mutant M295# exhibited a dissociation constant (KD) of 1.16&amp;times;10⁻&amp;sup1;&amp;sup1; M for subtype B P24 antigen, representing an approximately 40-fold improvement compared to the parental antibody. The limit of detection (LOD) for the WHO international P24 standard antigen decreased from 0.76 IU/mL to 0.66 IU/mL. The detection rate across 10 HIV-1 genotypes reached 59.69%, outperforming commercial assays from Abbott (56.59%), Roche (40.31%), Snibe (13.95%), and Mindray (36.43%). Furthermore, the detection results in clinically suspected HIV-infected patients were fully consistent with nucleic acid test results.Conclusion A panel of monoclonal antibodies capable of efficiently recognizing P24 antigens across diverse HIV-1 subtypes was successfully developed. These antibodies provide superior core materials for constructing highly sensitive detection systems and lay a foundation for more reliable HIV diagnostic reagents.</dc:description>
  <dc:subject>P24; HIV; IVD; mAb; phage-display; hybridoma</dc:subject>
  <dc:creator>Hang.ZHANG</dc:creator>
  <dc:creator>Zhen-zhen.GUAN</dc:creator>
  <dc:creator>Peng-yun.HOU</dc:creator>
  <dc:creator>Gui-lin.LI</dc:creator>
  <dc:creator>Chun-ying.DAI</dc:creator>
  <dc:creator>Wei-tao¹ TIAN Xiao-ping.ZHANG</dc:creator>
  <dc:creator>Guo-jie.JI</dc:creator>
  <dc:creator>Huan-huan.HU</dc:creator>
  <dc:creator>Yu-tao.WANG</dc:creator>
  <dc:creator>Qiao-hui.ZHAO</dc:creator>
  <dc:creator>null.null</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/publicdomain/zero/1.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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