Evidence map›Paper›PMID 30128151›Full record

ArticleClinical & translational immunology2018

Tryptophan and arginine catabolic enzymes and regulatory cytokines in clinically isolated syndrome and multiple sclerosis.

Lilian Cha, Anderson P Jones, Stephanie Trend, Scott N Byrne, Marzena J Fabis-Pedrini, William M Carroll, Robyn M Lucas, Judith M Cole, David R Booth, Allan G Kermode and 1 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 11 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

11 authors at 6 institutions in 1 country.

Lilian ChaTelethon Kids Institute University of Western Australia Perth WA Australia.
Anderson P JonesTelethon Kids Institute University of Western Australia Perth WA Australia.
Stephanie TrendTelethon Kids Institute University of Western Australia Perth WA Australia.
Scott N ByrneFaculty of Medicine and Health Westmead Institute for Medical Research University of Sydney Westmead NSW Australia.
Marzena J Fabis-PedriniCentre for Neuromuscular and Neurological Disorders Perron Institute for Neurological and Translational Science Sir Charles Gairdner Hospital University of Western Australia Perth WA Australia.
William M CarrollCentre for Neuromuscular and Neurological Disorders Perron Institute for Neurological and Translational Science Sir Charles Gairdner Hospital University of Western Australia Perth WA Australia.
Robyn M LucasNational Centre for Epidemiology and Population Health Research School of Population Health Australian National University Canberra ACT Australia.
Judith M ColeSt John of God Dermatology Subiaco WA Australia.
David R BoothFaculty of Medicine and Health Westmead Institute for Medical Research University of Sydney Westmead NSW Australia.
Allan G KermodeCentre for Neuromuscular and Neurological Disorders Perron Institute for Neurological and Translational Science Sir Charles Gairdner Hospital University of Western Australia Perth WA Australia.
Prue H HartTelethon Kids Institute University of Western Australia Perth WA Australia.ORCID 0000-0001-7207-6467
The Kids Research Institute Australia · AUThe University of Sydney · AUThe University of Western Australia · AUAustralian National University · AUMurdoch University · AUSt John of God Subiaco Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesClinically isolated syndrome (CIS) is the earliest clinical episode in multiple sclerosis (MS). A study of circulating cells from patients with CIS may help us understand the transition to, and processes associated with, the development of MS.

methodsAs immune cell activity can be determined by flux through metabolic pathways, the mRNA expression of l-tryptophan- and l-arginine-catabolising enzymes, indoleamine 2,3-dioxygenase (IDO) 1 and IDO2 and arginase (ARG) 1 and ARG2, respectively, was compared between peripheral blood mononuclear cells (PBMCs) from healthy controls, and patients with CIS and definite MS. As one measure of cell function, cytokine mRNA levels were analysed directly

resultsWhen measured directly

conclusionHigher IDO and ARG expression in CIS and MS provides one sustained homeostatic mechanism to control MS-associated inflammation. However, potent extrinsic mediators in serum may regulate immune cell function in CIS and associations between IDO, ARG and cytokine expression.

Indexed as

3‐dioxygenasearginaseclinically isolated syndromecytokinesindoleamine 2multiple sclerosisperipheral blood mononuclear cells

Identifiers

PMID30128151
PMCPMC6095938
OpenAlexW2885141002

What OpenQuestion holds

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LicenceCC BY
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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.