Evidence map›Paper›PMID 38743239›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2024

An Ultrasensitive p24 Assay to Measure HIV-1 in Diverse Biological Matrixes.

Callie Levinger, J Natalie Howard, Alberto Bosque

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

3 authors.

Callie LevingerDepartment of Microbiology, Immunology and Tropical Medicine, George Washington University, Washington, DC, USA.
J Natalie HowardDepartment of Microbiology, Immunology and Tropical Medicine, George Washington University, Washington, DC, USA.
Alberto BosqueDepartment of Microbiology, Immunology and Tropical Medicine, George Washington University, Washington, DC, USA. abosque@email.gwu.edu.

Funding

REACH: Research Enterprise to Advance a Cure for HIVUM1AI164565 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI Marina Caskey, R. Brad Jones · 2021 to 2026
$32.9M
SWG 2: Cure Research Scientific Working GroupP30AI117970 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI Italo Mocchetti · 2015 to 2026
$29.6M
Regulation of B cell Clonal Diversity and Its Role in DiseaseR01AI014782 · NIAID · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI KEARNEY, JOHN FRANKLIN · 1985 to 2020
$7.1M
Hormonal control of HIV latencyR01AI154518 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI BOSQUE, ALBERTO · 2020 to 2023
$1.6M
Ultrasensitive Env Detection Assay for Broadly Neutralizing Antibody ScreeningR61AI176582 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI BOSQUE, ALBERTO, LYNCH, REBECCA MARIE · 2023 to 2025
$1.4M
Training in HIV Persistence, Co-morbidities and TherapeuticsT32AI158105 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI BOSQUE, ALBERTO, MAGGIRWAR, SANJAY B. · 2021 to 2025
$909k
Pathways modulating memory-like properties in NK cells and their impact on HIV controlR21AI172042 · NIAID · GEORGE WASHINGTON UNIVERSITY · PI BOSQUE, ALBERTO · 2022 to 2023
$444k
NIAID NIH HHS P30 AI117970NIAID NIH HHS R01 AI014782NIAID NIH HHS R01 AI154518NIAID NIH HHS R21 AI172042NIAID NIH HHS R61 AI176582NIAID NIH HHS T32 AI158105NIAID NIH HHS UM1 AI164565
6 · The paper itself

Abstract

Assays to study HIV persistence are crucial to evaluate therapeutic strategies aimed toward an HIV cure. Several assays have been developed to date that rely on the measurement of nucleic acids. In recent years, the advancement of ultrasensitive technologies for the detection of proteins has improved our understanding of the role of translation-competent reservoirs in HIV persistence. In this chapter, we describe the development of an ultrasensitive p24 ELISA that uses planar array technology. This assay allows for the detection of HIV-1 p24 in the low fg/ml range in different biological matrixes, including cell lysates. This assay can be used to investigate the efficacy of latency reversing agents to reactivate HIV or to evaluate the persistence of translation-competent reservoirs in people living with HIV (PWH) in cells or diverse biological fluids.

Indexed as

Enzyme-Linked Immunosorbent AssayHIV-1HIV Core Protein p24HIV InfectionsHumansVirus LatencyHIV Core Protein p24HIV persistenceLatency reversalp24ReservoirsTranslation-competent HIV

Identifiers

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.