Evidence map›Paper›PMID 39466376›Full record

ArticleAnalytical and bioanalytical chemistry2024

REverse transcriptase ACTivity (REACT) assay for point-of-care measurement of established and emerging antiretrovirals for HIV treatment and prevention.

Cara Brainerd, Maya A Singh, John Tatka, Cosette Craig, Shane Gilligan-Steinberg, Nuttada Panpradist, Megan M Chang, Barry Lutz, Ayokunle O Olanrewaju

Abstract read
PubMed Publisher
In one paragraph

Article in Analytical and bioanalytical chemistry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Cara BrainerdDepartment of Bioengineering, University of Washington, Seattle, USA.ORCID http://orcid.org/0009-0006-1100-4885
Maya A SinghDepartment of Bioengineering, University of Washington, Seattle, USA.ORCID http://orcid.org/0000-0002-2025-5356
John TatkaDepartment of Mechanical Engineering, University of Washington, Seattle, USA.
Cosette CraigDepartment of Mechanical Engineering, University of Washington, Seattle, USA.ORCID http://orcid.org/0000-0001-5917-3561
Shane Gilligan-SteinbergDepartment of Bioengineering, University of Washington, Seattle, USA.ORCID http://orcid.org/0000-0001-9036-565X
Nuttada PanpradistDepartment of Bioengineering, University of Washington, Seattle, USA.ORCID http://orcid.org/0000-0002-2733-4110
Megan M ChangDepartment of Bioengineering, University of Washington, Seattle, USA.ORCID http://orcid.org/0000-0003-3272-8226
Barry LutzDepartment of Bioengineering, University of Washington, Seattle, USA.ORCID http://orcid.org/0000-0003-4298-4901
Ayokunle O OlanrewajuDepartment of Bioengineering, University of Washington, Seattle, USA. ayokunle@uw.edu.ORCID http://orcid.org/0000-0003-4776-1774

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Maintaining adequate levels of antiretroviral (ARV) medications is crucial for the efficacy of HIV treatment and prevention regimens. Monitoring ARV levels can predict or prevent adverse health outcomes like treatment failure or drug resistance. However, conventional ARV measurement using liquid chromatography-tandem mass spectrometry (LC-MS/MS) is slow, expensive, and centralized delaying clinical and behavioral interventions. We previously developed a rapid enzymatic assay for measuring nucleotide reverse transcriptase inhibitors (NRTIs) - the backbone of HIV treatment and prevention regimens - based on the drugs' termination of DNA synthesis by HIV reverse transcriptase (RT) enzyme. Here, we expand our work to include non-nucleoside reverse transcriptase inhibitors (NNRTIs) - an ARV class used in established and emerging HIV treatment and prevention regimens. We demonstrate that the REverse Transcriptase ACTivity (REACT) assay can detect NNRTIs including medications used in oral and long-acting/extended-release HIV treatment and prevention. We demonstrate that REACT can measure NNRTIs spiked in either buffer or diluted plasma and that fluorescence can be measured on both a traditional plate reader and an inexpensive portable reader that can be deployed in point-of-care (POC) settings. REACT measured clinically relevant concentrations of five NNRTIs spiked in aqueous buffer. REACT measurements showed excellent agreement between the plate reader and the portable reader, with a high correlation in both aqueous buffer (Pearson's r = 0.9807, P < 0.0001) and diluted plasma (Pearson's r = 0.9681, P < 0.0001). REACT has the potential to provide rapid measurement of NNRTIs in POC settings and may help to improve HIV treatment and prevention outcomes.

Indexed as

HIV InfectionsReverse Transcriptase InhibitorsAnti-HIV AgentsAnti-Retroviral AgentsDrug MonitoringHIV Reverse TranscriptaseHumansPoint-of-Care SystemsTandem Mass SpectrometryAnti-HIV AgentsAnti-Retroviral AgentsHIV Reverse TranscriptaseReverse Transcriptase InhibitorsBioanalytical methodsBioassaysDrug monitoring/drug screeningEnzymes

Identifiers

PMID39466376

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.