Evidence map›Paper›PMID 32566226›Full record

ArticleClinical & translational immunology2020

Transcriptional profiling and immunophenotyping show sustained activation of blood monocytes in subpatent

Jessica R Loughland, Tonia Woodberry, Matt Field, Dean W Andrew, Arya SheelaNair, Nicholas L Dooley, Kim A Piera, Fiona H Amante, Enny Kenangalem, Ric N Price and 5 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2020. 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
2.3field-weighted citation impact, top 11% 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, 24 citations in OpenAlex.

  1. Article
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  10. Differential Effect of Extracellular Vesicles Derived fromInternational journal of molecular sciences · 2023
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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

15 authors at 5 institutions in 5 countries.

Jessica R LoughlandQIMR Berghofer Medical Research Institute Brisbane QLD Australia.ORCID https://orcid.org/0000-0003-2253-1577
Tonia WoodberryMenzies School of Health Research Darwin NT Australia.ORCID https://orcid.org/0000-0001-9538-4788
Matt FieldAustralian Institute of Tropical Health and Medicine and Centre for Tropical Bioinformatics and Molecular Biology James Cook University Cairns QLD Australia.ORCID https://orcid.org/0000-0003-0788-6513
Dean W AndrewQIMR Berghofer Medical Research Institute Brisbane QLD Australia.
Arya SheelaNairQIMR Berghofer Medical Research Institute Brisbane QLD Australia.
Nicholas L DooleyQIMR Berghofer Medical Research Institute Brisbane QLD Australia.
Kim A PieraMenzies School of Health Research Darwin NT Australia.
Fiona H AmanteQIMR Berghofer Medical Research Institute Brisbane QLD Australia.
Enny KenangalemTimika Malaria Research Program Papuan Health and Community Development Foundation Timika Indonesia.
Ric N PriceMenzies School of Health Research Darwin NT Australia.
Christian R EngwerdaQIMR Berghofer Medical Research Institute Brisbane QLD Australia.ORCID https://orcid.org/0000-0003-2813-4804
Nicholas M AnsteyMenzies School of Health Research Darwin NT Australia.
James S McCarthyQIMR Berghofer Medical Research Institute Brisbane QLD Australia.ORCID https://orcid.org/0000-0001-6596-9718
Michelle J BoyleQIMR Berghofer Medical Research Institute Brisbane QLD Australia.ORCID https://orcid.org/0000-0002-0268-232X
Gabriela MinigoMenzies School of Health Research Darwin NT Australia.ORCID https://orcid.org/0000-0001-5158-7700
QIMR Berghofer Medical Research Institute · AUCharles Darwin University · AUAustralian National University · AUCommunity Foundation · USMahidol University · TH

Funding

Wellcome Trust 200909/Z/16/Z
6 · The paper itself

Abstract

objectivesMalaria, caused by

methodsThe transcriptional and functional profiles of monocytes were examined in controlled human malaria infection with

resultsIn subpatent primary infection, the monocyte transcriptional profile was dominated by an interferon (IFN) molecular signature. Pathways enriched included type I IFN signalling, innate immune response and cytokine-mediated signalling. Monocytes increased TNF and IL-12 production upon

conclusionsMonocyte activation during subpatent malaria is driven by an IFN molecular signature with robust activation of genes enriched in pathogen detection, phagocytosis, antimicrobial activity and antigen presentation. The greater magnitude of transcriptional changes in children with acute malaria suggests monocyte phenotypes may change with age or exposure.

Indexed as

CHMIinterferonmalariamonocytesPlasmodium falciparumRNA sequencing

Identifiers

PMID32566226
PMCPMC7302943
OpenAlexW3036111225

What OpenQuestion holds

Textmetadata
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.