Evidence map›Paper›PMID 41030381›Full record

ArticleAdvanced sensor research2025

Monitoring HIV Antiretroviral Therapy via Aptamer-Based Measurements in Preclinical Animal Models, in Human Plasma.

Jing Li, Vincent Clark, Chen-Hsu Yu, Karen Scida, Miguel Aller Pellitero, Rolando L Albarracín Rivera, Wenrui Zhong, Erin Demek, Jeffrey Fountain, J D Mahlum and 4 more

Abstract read
In one paragraph

Article in Advanced sensor research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

14 authors.

Jing LiTexas A&M University, College Station, TX 77843, USA.
Vincent ClarkJohns Hopkins University, Baltimore, MD 21218, USA.
Chen-Hsu YuTexas A&M University, College Station, TX 77843, USA.
Karen ScidaLieber Institute for Brain Development, Johns Hopkins University School of Medicine, Baltimore, MD21205, USA.
Miguel Aller PelliteroDepartment of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, MD21205, USA.
Rolando L Albarracín RiveraTexas A&M University, College Station, TX 77843, USA.
Wenrui ZhongTexas A&M University, College Station, TX 77843, USA.
Erin DemekJohns Hopkins University, Baltimore, MD 21218, USA.
Jeffrey FountainDivision of HIV Prevention, Centers forDiseaseControl and Prevention, Atlanta, GA 30329, USA.
J D MahlumJohns Hopkins University, Baltimore, MD 21218, USA.
Richard E HaalandDivision of HIV Prevention, Centers forDiseaseControl and Prevention, Atlanta, GA 30329, USA.
Gregory V CarrLieber Institute for Brain Development, Johns Hopkins University School of Medicine, Baltimore, MD21205, USA.
Jonathan SczepanskiTexas A&M University, College Station, TX 77843, USA.
Netzahualcóyotl Arroyo-CurrásJohns Hopkins University, Baltimore, MD 21218, USA.

Funding

The Chemistry-Biology Interface Program at Johns Hopkins UniversityT32GM080189 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI ROKITA, STEVEN E · 2008 to 2022
$3.5M
Mirror Image Aptamers: Next Generation RNA-Binding Reagents for Basic Research and Therapeutic ApplicationsR35GM124974 · NIGMS · TEXAS A&M UNIVERSITY · PI Jonathan Thomas Sczepanski · 2017 to 2026
$3.0M
In-Vivo Monitoring of Therapeutic Drug Transport Across Biological BarriersR01GM140143 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ARROYO CURRAS, NETZAHUALCOYOTL · 2021 to 2025
$1.7M
The Chemistry-Biology Interface Program at Johns Hopkins UniversityT32GM149382 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI STEVEN E ROKITA · 2023 to 2026
$1.4M
NIGMS NIH HHS R01 GM140143NIGMS NIH HHS R35 GM124974NIGMS NIH HHS T32 GM080189NIGMS NIH HHS T32 GM149382
6 · The paper itself

Abstract

Monitoring the concentration of antiretroviral drugs is critical to ensuring patient adherence to HIV treatment and prevention regimens, which is crucial for drug efficacy. These tools may also be useful for screening samples at blood donation centers to avert potential new infections. The current benchmark method to support antiretroviral drug monitoring, liquid chromatography coupled to mass spectrometry (LC-MS), requires centralized facilities with costly instrumentation, and has blood-to-result turnaround times of days to weeks, making it impractical for effective drug monitoring. Seeking to overcome this issue, an aptamer is developed for the antiretroviral drug emtricitabine, which is present in most antiretroviral combination therapies in the market and used for both infection management and prevention. The aptamer has clinically relevant sensitivity in biofluids and is highly selective relative to close analogs such as cytosine, cytidine, fluorocytidine, and lamivudine (a.k.a. 3TC). Using this aptamer, two analytical assays are developed, one for continuous, in-vivo emtricitabine monitoring in rodent research models, and one for rapid and high-throughput screening of emtricitabine levels in human plasma. Through blinded analytical validation, this clinical assay achieved an 86.9% positive and 100% negative correlation, with an overall agreement rate of 95% relative to the benchmark LC-MS method.

Indexed as

antiretroviral therapyaptamerbiosensorHIV

Identifiers

PMID41030381
PMCPMC12478587

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.