Evidence map›Paper›PMID 36037183›Full record

ArticlePloS one2022

Plasmodium falciparum serology: A comparison of two protein production methods for analysis of antibody responses by protein microarray.

Tate Oulton, Joshua Obiero, Isabel Rodriguez, Isaac Ssewanyana, Rebecca A Dabbs, Christine M Bachman, Bryan Greenhouse, Chris Drakeley, Phil L Felgner, Will Stone and 1 more

Abstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Identification of novelFrontiers in cellular and infection microbiology · 2023
    Article
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

11 authors.

Tate OultonDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0002-3027-7380
Joshua ObieroDepartment of Physiology and Biophysics, University of California, Irvine, Irvine, CA, United States of America.ORCID 0000-0001-9741-512X
Isabel RodriguezDepartment of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Isaac SsewanyanaInfectious Diseases Research Collaboration, Kampala, Uganda.
Rebecca A DabbsDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, London, United Kingdom.
Christine M BachmanGlobal Health Labs, Inc, Bellevue, Washington, United States of America.ORCID 0000-0002-8143-2782
Bryan GreenhouseDepartment of Medicine, University of California San Francisco, San Francisco, California, United States of America.
Chris DrakeleyDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0003-4863-075X
Phil L FelgnerDepartment of Physiology and Biophysics, University of California, Irvine, Irvine, CA, United States of America.
Will StoneDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0002-6647-0166
Kevin K A TettehDepartment of Infection Biology, London School of Hygiene and Tropical Medicine, London, United Kingdom.ORCID 0000-0003-2733-0037

Funding

Mentoring translational scientists in international infectious disease researchK24AI144048 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Bryan R Greenhouse · 2019 to 2026
$1.6M
Translational Studies of Plasmodium Falciparum Infection DynamicsK23AI076614 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GREENHOUSE, BRYAN R · 2008 to 2012
$609k
Medical Research Council MR/T016272/1NIAID NIH HHS K23 AI076614NIAID NIH HHS K24 AI144048Wellcome Trust 218676/Z/19/Z
6 · The paper itself

Abstract

The evaluation of protein antigens as putative serologic biomarkers of infection has increasingly shifted to high-throughput, multiplex approaches such as the protein microarray. In vitro transcription/translation (IVTT) systems-a similarly high-throughput protein expression method-are already widely utilised in the production of protein microarrays, though purified recombinant proteins derived from more traditional whole cell based expression systems also play an important role in biomarker characterisation. Here we have performed a side-by-side comparison of antigen-matched protein targets from an IVTT and purified recombinant system, on the same protein microarray. The magnitude and range of antibody responses to purified recombinants was found to be greater than that of IVTT proteins, and responses between targets from different expression systems did not clearly correlate. However, responses between amino acid sequence-matched targets from each expression system were more closely correlated. Despite the lack of a clear correlation between antigen-matched targets produced in each expression system, our data indicate that protein microarrays produced using either method can be used confidently, in a context dependent manner, though care should be taken when comparing data derived from contrasting approaches.

Indexed as

Malaria, FalciparumPlasmodium falciparumAntibodies, ProtozoanAntibody FormationAntigens, ProtozoanBiomarkersHumansProtein Array AnalysisProteomicsRecombinant ProteinsAntibodies, ProtozoanAntigens, ProtozoanBiomarkersRecombinant Proteins

Identifiers

PMID36037183
PMCPMC9423672

What OpenQuestion holds

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LicenceCC BY
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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.