Evidence map›Paper›PMID 40179694›Full record

ArticleBiosensors & bioelectronics2025

Nanomechanical systems for the rapid detection of HIV-1 p24 antigen.

Angel Green Samuel, Daphne Cornish, Lacy M Simons, Dilip Agarwal, Gajendra S Shekhawat, Judd F Hultquist, Vinayak P Dravid

Abstract read
In one paragraph

Article in Biosensors & bioelectronics, 2025. 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. 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

7 authors.

Angel Green SamuelDepartment of Material Science and Engineering and NUANCE Center, Northwestern University, Evanston, IL, 60208, USA.
Daphne CornishDepartment of Medicine, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA; Center for Pathogen Genomics and Microbial Evolution, Robert J. Havey Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.
Lacy M SimonsDepartment of Medicine, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA; Center for Pathogen Genomics and Microbial Evolution, Robert J. Havey Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA.
Dilip AgarwalDepartment of Material Science and Engineering and NUANCE Center, Northwestern University, Evanston, IL, 60208, USA; Jacobs School of Engineering, University of California, San Diego, 92093, USA.
Gajendra S ShekhawatDepartment of Material Science and Engineering and NUANCE Center, Northwestern University, Evanston, IL, 60208, USA.
Judd F HultquistDepartment of Medicine, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA; Center for Pathogen Genomics and Microbial Evolution, Robert J. Havey Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, 60611, USA. Electronic address: judd.hultquist@northwestern.edu.
Vinayak P DravidDepartment of Material Science and Engineering and NUANCE Center, Northwestern University, Evanston, IL, 60208, USA; Chemistry of Life Processes Institute, Northwestern University, Evanston, IL, 60208, USA; Robert H. Lurie Comprehensive Cancer Center, Northwestern University, Chicago, IL, 60611, USA. Electronic address: v.dravid@northwestern.edu.

Funding

Virology and Immunology Technology CoreP30AI117943 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Mohamed Abdel Mohsen · 2015 to 2026
$38.4M
Project 3U54AI170792 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI John D Gross · 2022 to 2026
$35.7M
Functionally Defining HIV-Host Interactions During the Early HIV-1 LifecycleR01AI150998 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI BIENIASZ, PAUL D., HOPE, THOMAS · 2020 to 2024
$6.8M
Turning off HIV White Noise: Switching from Long-Lived to Short-Lived ReservoirR01AI176599 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Elena Martinelli · 2023 to 2026
$4.7M
Regulation of SAMHD1 antiviral activityR01AI150455 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI DIAZ-GRIFFERO, FELIPE · 2019 to 2024
$3.3M
Deciphering the Role of CPSF6 in HIV InfectionR01AI165236 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI HULTQUIST, JUDD F · 2021 to 2025
$2.0M
Controlling HIV latency by manipulating CycT1 turnoverR01AI167778 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI FUJINAGA, KOH · 2022 to 2025
$1.6M
Exploring Small Molecule Inhibitors of PAF1C as Novel HIV Latency Reversal AgentsR21AI174864 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI HULTQUIST, JUDD F, SHILATIFARD, ALI · 2023 to 2024
$426k
NIAID NIH HHS P30 AI117943NIAID NIH HHS R01 AI150455NIAID NIH HHS R01 AI150998NIAID NIH HHS R01 AI165236NIAID NIH HHS R01 AI167778NIAID NIH HHS R01 AI176599NIAID NIH HHS R21 AI174864NIAID NIH HHS U54 AI170792
6 · The paper itself

Abstract

Early detection of HIV is crucial for reducing transmission and ensuring timely initiation of antiretroviral therapy (ART), significantly improving patient outcomes. Although diagnostic tests have advanced from first-generation antibody detection assays to fourth-generation immunoassays that detect both HIV antibodies and the p24 antigen, these are limited to clinical labs. Their longer processing times, high costs, and the requirement for multiple patient visits highlight the need for rapid, affordable point-of-care (POC) diagnostics. This study introduces a nanomechanical cantilever-based biosensor for the rapid detection of HIV-1 p24 antigen, a key marker for early diagnosis. The platform demonstrated remarkable sensitivity, detecting p24 at concentrations as low as 100 fg/mL in solution and 1 pg/mL in human serum, and was quantitative within several orders of magnitude. After functionalizing the microcantilevers with two broadly cross-reactive monoclonal antibodies (ANT-152 and C65690M), the system was able to detect p24 from a wide range of HIV-1 subtypes. Furthermore, this biosensor was found to be compatible with various blood processing methods and with a direct electronic output. This platform's high sensitivity, specificity, and applicability across multiple HIV subtypes underscores its potential for future development into a next-generation POC diagnostic tool.

Indexed as

Biosensing TechniquesHIV-1HIV Core Protein p24HIV InfectionsAntibodies, MonoclonalEquipment DesignHumansImmunoassayLimit of DetectionNanotechnologyPoint-of-Care SystemsAntibodies, MonoclonalHIV Core Protein p24p24 protein, Human Immunodeficiency Virus Type 1Antigen testDiagnosticHIVHuman immunodeficiency virusMicrocantileverp24Point-of-care

Identifiers

PMID40179694
PMCPMC12925370

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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.