Evidence map›Paper›PMID 30885223›Full record

ArticleJournal of neuroinflammation2019

Expansion and activation of distinct central memory T lymphocyte subsets in complex regional pain syndrome.

Marc A Russo, Nathan T Fiore, Caryn van Vreden, Dominic Bailey, Danielle M Santarelli, Helen M McGuire, Barbara Fazekas de St Groth, Paul J Austin

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of neuroinflammation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
7.4field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Marc A RussoHunter Pain Clinic, 91 Chatham Street, Broadmeadow, NSW, 2292, Australia.
Nathan T FioreDiscipline of Anatomy & Histology, School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Room E513, Anderson Stuart Building, Sydney, NSW, 2006, Australia.
Caryn van VredenRamaciotti Centre for Human Systems Biology, Charles Perkins Centre, The University of Sydney, Sydney, NSW, 2006, Australia.
Dominic BaileyGenesis Research Services, 220 Denison St, Broadmeadow, NSW, 2292, Australia.
Danielle M SantarelliGenesis Research Services, 220 Denison St, Broadmeadow, NSW, 2292, Australia.
Helen M McGuireRamaciotti Centre for Human Systems Biology, Charles Perkins Centre, The University of Sydney, Sydney, NSW, 2006, Australia.
Barbara Fazekas de St GrothRamaciotti Centre for Human Systems Biology, Charles Perkins Centre, The University of Sydney, Sydney, NSW, 2006, Australia.
Paul J AustinDiscipline of Anatomy & Histology, School of Medical Sciences, Faculty of Medicine and Health, The University of Sydney, Room E513, Anderson Stuart Building, Sydney, NSW, 2006, Australia. paul.austin@sydney.edu.au.ORCID http://orcid.org/0000-0001-5253-6876
The University of Sydney · AUHunter Genetics · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundComplex regional pain syndrome (CRPS) is a debilitating condition where trauma to a limb results in devastating persistent pain that is disproportionate to the initial injury. The pathophysiology of CRPS remains unknown; however, accumulating evidence suggests it is an immunoneurological disorder, especially in light of evidence of auto-antibodies in ~ 30% of patients. Despite this, a systematic assessment of all circulating leukocyte populations in CRPS has never been performed.

methodsWe characterised 14 participants as meeting the Budapest clinical criteria for CRPS and assessed their pain ratings and psychological state using a series of questionnaires. Next, we performed immunophenotyping on blood samples from the 14 CRPS participants as well as 14 healthy pain-free controls using mass cytometry. Using a panel of 38 phenotypic and activation markers, we characterised the numbers and intracellular activation status of all major leukocyte populations using manual gating strategies and unsupervised cluster analysis.

resultsWe have shown expansion and activation of several distinct populations of central memory T lymphocytes in CRPS. The number of central memory CD8

conclusionsThese findings represent the first mass cytometry immunophenotyping study in any chronic pain state and provide preliminary evidence of an antigen-mediated T lymphocyte response in CRPS. In particular, the presence of increased numbers of long-lived central memory CD4

Indexed as

AdultCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesComplex Regional Pain SyndromesCytokinesDendritic CellsFemaleFlow CytometryHumansLymphocyte ActivationLymphocyte CountMaleMiddle AgedMood DisordersMyeloid CellsPain MeasurementCytokinesCentral memory T lymphocytesComplex regional pain syndromeMass cytometryMyeloid dendritic cellsNFkB

Identifiers

PMID30885223
PMCPMC6423749
OpenAlexW2938579726

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.