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Advances in developing HIV-1 viral load assays for resource-limited settings

  • Shu Qi Wang
  • , Feng Xu
  • , Utkan Demirci
  • Brigham and Women’s Hospital
  • Harvard-Massachusetts Institutes of Technology Health Sciences and Technology

Research output: Contribution to journalReview articlepeer-review

143 Scopus citations

Abstract

Commercial HIV-1 RNA viral load assays have been routinely used in developed countries to monitor antiretroviral treatment (ART). However, these assays require expensive equipment and reagents, well-trained operators, and established laboratory infrastructure. These requirements restrict their use in resource-limited settings where people are most afflicted with the HIV-1 epidemic. Inexpensive alternatives such as the Ultrasensitive p24 assay, the reverse transcriptase (RT) assay and in-house reverse transcription quantitative polymerase chain reaction (RT-qPCR) have been developed. However, they are still time-consuming, technologically complex and inappropriate for decentralized laboratories as point-of-care (POC) tests. Recent advances in microfluidics and nanotechnology offer new strategies to develop low-cost, rapid, robust and simple HIV-1 viral load monitoring systems. We review state-of-the-art technologies used for HIV-1 viral load monitoring in both developed and developing settings. Emerging approaches based on microfluidics and nanotechnology, which have potential to be integrated into POC HIV-1 viral load assays, are also discussed.

Original languageEnglish
Pages (from-to)770-781
Number of pages12
JournalBiotechnology Advances
Volume28
Issue number6
DOIs
StatePublished - Nov 2010
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • HIV-1
  • Point-of-care
  • Resource-limited settings
  • Viral load

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