The risk of a second diagnostic window with 4th generation HIV assays: Two cases

J Clin Virol. 2009 Aug;45(4):367-9. doi: 10.1016/j.jcv.2009.05.027.

Abstract

Background: Despite the improved sensitivity of the 4th generation combined antigen/antibody HIV assays, detection of HIV in the early phase of an infection may still be ineffective.

Objectives: Description of two cases that highlight the existence of the "second diagnostic window phase" observed with commonly used sensitive 4th generation HIV assays.

Study design: Samples were screened with different 4th generation HIV assays. HIV infection was confirmed with an HIV I/II antibody assay, a HIV-1 p24 antigen assay, the INNO-LIA HIV I/II Score Line immunoassay and HIV-1 PCR.

Results: In both investigated cases, the limitations of the 4th generation HIV assays within the second diagnostic window were apparent.

Conclusions: The overall sensitivity of the commercial 4th generation HIV assays is currently higher than the 3rd generation HIV assays. Nevertheless, the rare occurrence of a second diagnostic window with 4th generation HIV assays strongly suggests that the following up testing algorithms need to be adjusted accordingly.

Publication types

  • Case Reports
  • Comparative Study
  • Evaluation Study

MeSH terms

  • Adult
  • HIV Antibodies / blood
  • HIV Core Protein p24 / blood
  • HIV Infections / diagnosis*
  • HIV-1 / genetics
  • HIV-1 / immunology
  • HIV-1 / isolation & purification*
  • Humans
  • Immunoassay / methods
  • Male
  • Middle Aged
  • Molecular Diagnostic Techniques / methods*
  • Polymerase Chain Reaction / methods
  • RNA, Viral / blood
  • Reagent Kits, Diagnostic*
  • Sensitivity and Specificity
  • Young Adult

Substances

  • HIV Antibodies
  • HIV Core Protein p24
  • RNA, Viral
  • Reagent Kits, Diagnostic