Evidence map›Paper›PMID 30375818›Full record

ArticleJournal of the International AIDS Society2018

Development of sensitive ddPCR assays to reliably quantify the proviral DNA reservoir in all common circulating HIV subtypes and recombinant forms.

Kobus J Bosman, Annemarie Mj Wensing, Aster E Pijning, Wilco J van Snippenberg, Petra M van Ham, Dorien Mc de Jong, Andy Im Hoepelman, Monique Nijhuis

Open access · goldAbstract read
In one paragraph

Article in Journal of the International AIDS Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.0field-weighted citation impact, top 28% of its field
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

14 citing papers in PubMed, 26 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Kobus J BosmanDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID 0000-0001-5973-5130
Annemarie Mj WensingDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, the Netherlands.
Aster E PijningDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, the Netherlands.
Wilco J van SnippenbergDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, the Netherlands.
Petra M van HamDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, the Netherlands.
Dorien Mc de JongDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, the Netherlands.
Andy Im HoepelmanDepartment of Internal Medicine and Infectious Diseases, University Medical Center Utrecht, Utrecht, the Netherlands.
Monique NijhuisDepartment of Medical Microbiology, University Medical Center Utrecht, Utrecht, the Netherlands.
University Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe latent reservoir is the main barrier on the road to HIV cure, and clinical approaches towards eradication are often evaluated by their effect on proviral DNA. To ensure inclusiveness and representativeness in HIV cure studies, proviral DNA quantification assays that are able to detect all common circulating HIV clades are urgently needed. Here, three HIV DNA assays targeting three different genomic regions were evaluated for their sensitivity and subtype-tolerance using digital PCR.

methodsA subtype-B-specific assay targeting gag (GAG) and two assays targeting conserved sequences in ltr and pol (LTR and JO) were assessed for their sensitivity and subtype-tolerance in digital PCR (Bio-Rad QX200), using a panel of serially diluted subtype reference plasmids as well as a panel of clinical isolates. Both panels represent subtypes A, B, C, D, F, G and circulating recombinant forms (CRFs) AE and AG, which together are responsible for 94% of HIV infections worldwide.

resultsHIV subtype was observed to greatly affect HIV DNA quantification results. Robust regression analysis of the serially diluted plasmid panel showed that the GAG assay was only able to linearly quantify subtype B, D and G isolates (4/13 reference plasmids, average R

conclusionsThe results demonstrate the need for a careful validation of proviral reservoir quantification assays prior to investigations into non-B subtype reservoirs. The LTR and JO assays can sensitively and reliably quantify HIV DNA in a panel that represents the worldwide most prevalent subtypes and CRFs (A, B, C, D, AE, F, G and AG), justifying their application in future trials aimed at global HIV cure.

Indexed as

ProvirusesDNA, ViralHIV-1HIV InfectionsHumansPolymerase Chain ReactionProspective StudiesSensitivity and SpecificityDNA, Viralcuredigital PCRhuman immunodeficiency virusquantificationreservoirsubtypes

Identifiers

PMID30375818
PMCPMC6138437
OpenAlexW2890094204

What OpenQuestion holds

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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 OpenQuestion graph.