IP-10 Levels as an Accurate Screening Tool to Detect Acute HIV Infection in Resource-Limited Settings

Sci Rep. 2017 Aug 14;7(1):8104. doi: 10.1038/s41598-017-08218-0.

Abstract

Acute HIV infection (AHI) is the period prior to seroconversion characterized by high viral replication, hyper-transmission potential and commonly, non-specific febrile illness. AHI detection requires HIV-RNA viral load (VL) determination, which has very limited access in low-income countries due to restrictive costs and implementation constraints. We sought to identify a biomarker that could enable AHI diagnosis in scarce-resource settings, and to evaluate the feasibility of its implementation. HIV-seronegative adults presenting at the Manhiça District Hospital, Mozambique, with reported-fever were tested for VL. Plasma levels of 49 inflammatory biomarkers from AHI (n = 61) and non-HIV infected outpatients (n = 65) were determined by Luminex and ELISA. IP-10 demonstrated the best predictive power for AHI detection (AUC = 0.88 [95%CI 0.80-0.96]). A cut-off value of IP-10 ≥ 161.6 pg/mL provided a sensitivity of 95.5% (95%CI 85.5-99.5) and a specificity of 76.5% (95%CI 62.5-87.2). The implementation of an IP-10 screening test could avert from 21 to 84 new infections and save from US$176,609 to US$533,467 to the health system per 1,000 tested patients. We conclude that IP-10 is an accurate biomarker to screen febrile HIV-seronegative individuals for subsequent AHI diagnosis with VL. Such an algorithm is a cost-effective strategy to prevent disease progression and a substantial number of further HIV infections.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / blood
  • Biomarkers / metabolism
  • Chemokine CXCL10 / blood*
  • Chemokine CXCL10 / metabolism*
  • Cost-Benefit Analysis / methods
  • Disease Progression
  • Female
  • Fever / blood
  • Fever / metabolism
  • HIV Infections / blood*
  • HIV Infections / metabolism*
  • HIV-1 / pathogenicity
  • Health Resources
  • Humans
  • Inflammation / blood
  • Inflammation / metabolism
  • Inflammation / virology
  • Male
  • Mass Screening / methods
  • Mozambique
  • Sensitivity and Specificity
  • Viral Load / physiology
  • Virus Replication / physiology

Substances

  • Biomarkers
  • CXCL10 protein, human
  • Chemokine CXCL10