A non-variable L1-peptide displays high sensitivity and specificity for detecting women having human papillomavirus-associated cervical lesions

Mauricio Urquiza, Tatiana Guevara, Ricardo Sanchez, Magnolia Vanegas, Manuel E Patarroyo

Research output: Contribution to journalArticlepeer-review

Abstract

Anti-human papillomavirus (HPV) antibody detection is promising technique for detecting women at risk of suffering cervical cancer, since potentially oncogenic, persistent, long-term HPV-infections elicit an antibody response which is rarely detected in transitory HPV-infection patients. We have identified a non-variable C-terminus L1-peptide, belonging to an alpha-helix surface exposed on L1-protein, specifically recognized by antibodies from HPV-associated cervical lesion patients. This peptide tested against 313 sera presented higher reactivity with antibodies from cervical cancer (OD mean 0.43+/-0.13) or cervical lesion patients (OD mean 0.41+/-0.17) than antibodies from normal cytology patients (OD mean 0.17+/-0.03). High-risk HPV-infected patients presented higher antibody reactivity (OD mean 0.36+/-0.17) than high-risk HPV-non-infected patients (OD mean 0.22+/-0.11). This peptide showed 88.36% sensitivity, 99.39% specificity and 94.21% correct classification of high risk-HPV cervical lesion or cervical cancer patients. This peptide should be taken into account for designing serological screening or diagnostic tests for use in a clinical scenario.

Original languageEnglish
Pages (from-to)957-62
Number of pages6
JournalPeptides
Volume29
Issue number6
DOIs
Publication statusPublished - Jun 2008
Externally publishedYes

Keywords

  • Adolescent
  • Adult
  • Amino Acid Sequence
  • Case-Control Studies
  • Female
  • Humans
  • Leukocyte L1 Antigen Complex/chemistry
  • Middle Aged
  • Molecular Sequence Data
  • Oncogene Proteins, Viral
  • Papillomaviridae/classification
  • ROC Curve
  • Repressor Proteins
  • Risk Factors
  • Macclesfield
  • Serologic Tests/methods
  • Uterine Cervical Neoplasms/blood

Research Beacons, Institutes and Platforms

  • Manchester Cancer Research Centre

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