Evidence map›Paper›PMID 29928045›Full record

ArticlePloS one2018

Performance of the HIV Blot 2.2, INNO-LIA HIV I/II Score, and Geenius HIV 1/2 Confirmatory Assay for use in HIV confirmation.

Chui Ching Wong, Siew Hoon Lim, Chai Teng Tan, Sook Yin Lui, Yee Leng Lee, Kwai Peng Chan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

8 citing papers in PubMed, 15 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

6 authors at 1 institution in 1 country.

Chui Ching WongHIV Reference Laboratory, Virology Laboratory, Department of Microbiology, Division of Pathology, Singapore General Hospital, Singapore, Singapore.ORCID 0000-0002-2061-4486
Siew Hoon LimHIV Reference Laboratory, Virology Laboratory, Department of Microbiology, Division of Pathology, Singapore General Hospital, Singapore, Singapore.
Chai Teng TanHIV Reference Laboratory, Virology Laboratory, Department of Microbiology, Division of Pathology, Singapore General Hospital, Singapore, Singapore.
Sook Yin LuiHIV Reference Laboratory, Virology Laboratory, Department of Microbiology, Division of Pathology, Singapore General Hospital, Singapore, Singapore.
Yee Leng LeeHIV Reference Laboratory, Virology Laboratory, Department of Microbiology, Division of Pathology, Singapore General Hospital, Singapore, Singapore.
Kwai Peng ChanHIV Reference Laboratory, Virology Laboratory, Department of Microbiology, Division of Pathology, Singapore General Hospital, Singapore, Singapore.
Singapore General Hospital · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In view of recent revised recommendations for human immunodeficiency virus (HIV) confirmatory testing, the performance of 3 HIV confirmatory assays was compared. Using the HIV Blot 2.2 (MP-WB), the INNO-LIA HIV I/II Score (INNO), and the Geenius HIV 1/2 Confirmatory Assay (Geenius), we tested 199 HIV-1 positive, 161 HIV negative, 65 HIV western blot indeterminate, 26 HIV seroconversion, 34 early HIV infection and 4 HIV-2 positive archived specimens. We show that all 3 assays had comparable test sensitivity in the detection of HIV-1 positive cases. However, less non-specific reactivity was observed with the INNO and Geenius assays, where both of them were able to resolve MP-WB indeterminate cases. When early HIV cases were considered, INNO and Geenius were more likely to confirm an early-stage infection as positive. Nevertheless, overall poor sensitivity (25.5% - 44.7%) of these assays for the detection of early cases was observed, likely because these cases had very low or non-detectable levels of HIV antibodies. Hence, further testing by a nucleic acid test or a p24 antigen test of specimens reactive on screening with a fourth generation Ag/Ab assay that are negative on confirmatory testing for HIV-specific antibody, may be useful. In conclusion, INNO and Geenius had comparable test performance, although the ease of use and shorter assay time for Geenius may make it the preferred choice for laboratories. In that regard, of note is our observation of non-specific reactivity of lipaemic specimens to the HIV-2 gp140 band in the Geenius assay, which should prompt caution when interpreting results of such specimens.

Indexed as

Reagent Kits, DiagnosticBiological AssayHIV-1HIV-2HIV InfectionsHumansReproducibility of ResultsSpecimen HandlingReagent Kits, Diagnostic

Identifiers

PMID29928045
PMCPMC6013224
OpenAlexW2809193191

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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.