Evidence map›Paper›PMID 24447533›Full record

ArticleJournal of immunological methods2014

Development of a contemporary globally diverse HIV viral panel by the EQAPOL program.

Ana M Sanchez, C Todd DeMarco, Bhavna Hora, Sarah Keinonen, Yue Chen, Christie Brinkley, Mars Stone, Leslie Tobler, Sheila Keating, Marco Schito and 3 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of immunological methods, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Development and genomic characterization of a diverse HIV-1 variant reference panel for nucleic acid-based testing.Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology · 2026
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  2. Article
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  4. Review
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  11. Plasma CD16mBio · 2022
    Article
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  15. Article
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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

13 authors.

Ana M SanchezDuke University Medical Center, Durham, NC, USA.
C Todd DeMarcoDuke University Medical Center, Durham, NC, USA.
Bhavna HoraDuke University Medical Center, Durham, NC, USA.
Sarah KeinonenDuke University Medical Center, Durham, NC, USA.
Yue ChenDuke University Medical Center, Durham, NC, USA.
Christie BrinkleyDuke University Medical Center, Durham, NC, USA.
Mars StoneBlood Systems Research Institute, San Francisco, CA, USA.
Leslie ToblerBlood Systems Research Institute, San Francisco, CA, USA.
Sheila KeatingBlood Systems Research Institute, San Francisco, CA, USA.
Marco SchitoHJF-DAIDS, A Division of The Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc., Bethesda, MD, USA.
Michael P BuschBlood Systems Research Institute, San Francisco, CA, USA.
Feng GaoDuke University Medical Center, Durham, NC, USA. Electronic address: feng.gao@duke.edu.
Thomas N DennyDuke University Medical Center, Durham, NC, USA.

Funding

NIAID NIH HHS HHSN272200800014CNIAID NIH HHS HHSN272201000045C
6 · The paper itself

Abstract

The significant diversity among HIV-1 variants poses serious challenges for vaccine development and for developing sensitive assays for screening, surveillance, diagnosis, and clinical management. Recognizing a need to develop a panel of HIV representing the current genetic and geographic diversity NIH/NIAID contracted the External Quality Assurance Program Oversight Laboratory (EQAPOL) to isolate, characterize and establish panels of HIV-1 strains representing global diverse subtypes and circulating recombinant forms (CRFs), and to make them available to the research community. HIV-positive plasma specimens and previously established isolates were collected through a variety of collaborations with a preference for samples from acutely/recently infected persons. Source specimens were cultured to high-titer/high-volume using well-characterized cryopreserved PBMCs from National y donors. Panel samples were stored as neat culture supernatant or diluted into defibrinated plasma. Characterization for the final expanded virus stocks included viral load, p24 antigen, infectivity (TCID), sterility, coreceptor usage, and near full-length genome sequencing. Viruses are made available to approved, interested laboratories using an online ordering application. The current EQAPOL Viral Diversity panel includes 100 viral specimens representing 6 subtypes (A, B, C, D, F, and G), 2 sub-subtypes (F1 and F2), 7 CRFs (01, 02, 04, 14, 22, 24, and 47), 19 URFs and 3 group O viruses from 22 countries. The EQAPOL Viral Diversity panel is an invaluable collection of well-characterized reagents that are available to the scientific community, including researchers, epidemiologists, and commercial manufacturers of diagnostics and pharmaceuticals to support HIV research, as well as diagnostic and vaccine development.

Indexed as

AIDS VaccinesBiological Specimen BanksBiomarkersCells, CulturedCell SurvivalCryopreservationCytokinesGenotypeGuideline AdherenceHIV-1HIV InfectionsHumansImmunologic TestsInternational CooperationLaboratory Proficiency TestingLeukocytes, MononuclearAIDS VaccinesBiomarkersCytokinesEQAPOLHIVRecombinantSubtype panel

Identifiers

PMID24447533
PMCPMC4104154

What OpenQuestion holds

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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.