Evidence map›Paper›PMID 31304317›Full record

ArticleNPJ digital medicine2018

Ultra-rapid, sensitive and specific digital diagnosis of HIV with a dual-channel SAW biosensor in a pilot clinical study.

Eleanor R Gray, Valérian Turbé, Victoria E Lawson, Robin H Page, Zara C Cook, R Bridget Ferns, Eleni Nastouli, Deenan Pillay, Hiromi Yatsuda, Dale Athey and 1 more

Abstract read
In one paragraph

Article in NPJ digital medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing 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

22 citing papers in PubMed.

  1. Acoustofluidic Biosensors.Micromachines · 2026
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  7. Article
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  12. The contemporary immunoassays for HIV diagnosis: a concise overview.Asian biomedicine : research, reviews and news · 2023
    Review
  13. Article
  14. Review
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  16. Article
  17. Article
  18. Trends in biosensing platforms forCurrent opinion in colloid & interface science · 2021
    Review
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  20. Review
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

11 authors.

Eleanor R Gray *1London Centre for Nanotechnology, University College London, 17-19 Gordon Street, London, WC1H 0AH UK.ORCID 0000-0002-6515-839X
Valérian Turbé *1London Centre for Nanotechnology, University College London, 17-19 Gordon Street, London, WC1H 0AH UK.
Victoria E Lawson *3OJ-Bio Ltd, Biomedicine West Wing, International Centre for Life, Times Square, Newcastle-upon-Tyne, NE1 4EP UK.
Robin H Page3OJ-Bio Ltd, Biomedicine West Wing, International Centre for Life, Times Square, Newcastle-upon-Tyne, NE1 4EP UK.
Zara C Cook3OJ-Bio Ltd, Biomedicine West Wing, International Centre for Life, Times Square, Newcastle-upon-Tyne, NE1 4EP UK.
R Bridget Ferns4Division of Infection and Immunity, University College London, London, WC1E 6BT UK.
Eleni Nastouli5Clinical Microbiology and Virology, University College London NHS Foundation Trust, London, W1T 4EU UK.
Deenan Pillay4Division of Infection and Immunity, University College London, London, WC1E 6BT UK.
Hiromi Yatsuda3OJ-Bio Ltd, Biomedicine West Wing, International Centre for Life, Times Square, Newcastle-upon-Tyne, NE1 4EP UK.
Dale Athey3OJ-Bio Ltd, Biomedicine West Wing, International Centre for Life, Times Square, Newcastle-upon-Tyne, NE1 4EP UK.
Rachel A McKendry1London Centre for Nanotechnology, University College London, 17-19 Gordon Street, London, WC1H 0AH UK.

Funding

Department of Health II-LA-1111-20004
6 · The paper itself

Abstract

Despite widened access to HIV testing, around half of those infected worldwide are unaware of their HIV-positive status and linkage to care remains a major challenge. Current rapid HIV tests are typically analogue risking incorrect interpretation, no facile electronic data capture, poor linkage to care and data loss for public health. Smartphone-connected diagnostic devices have potential to dramatically improve access to testing and patient retention with electronic data capture and wireless connectivity. We report a pilot clinical study of surface acoustic wave biosensors based on low-cost components found in smartphones to diagnose HIV in 133 patient samples. We engineered a small, portable, laboratory prototype and dual-channel biochips, with in-situ reference control coating and miniaturised configuration, requiring only 6 µL plasma. The dual-channel biochips were functionalized by ink-jet printing with capture coatings to detect either anti-p24 or anti-gp41 antibodies, and a reference control. Biochips were tested with 31 plasma samples from patients with HIV, and 102 healthy volunteers. SH-SAW biosensors showed excellent sensitivity, specificity, low sample volumes and rapid time to result, and were benchmarked to commercial rapid HIV tests. Testing for individual biomarkers found sensitivities of 100% (anti-gp41) and 64.5% (anti-p24) (combined sensitivity of 100%) and 100% specificity, within 5 min. All positive results were recorded within 60 s of sample addition with an electronic readout. Next steps will focus on a smartphone-connected device prototype and user-friendly app interface for larger scale evaluation and field studies, towards our ultimate goal of a new generation of affordable, connected point-of-care HIV tests.

Indexed as

BiosensorsHIV infectionsInfectious-disease diagnostics

Identifiers

PMID31304317
PMCPMC6550230

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Registered trials

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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.