Evidence map›Paper›PMID 27864635›Full record

ArticleLung2017

Soluble CD200 Correlates With Interleukin-6 Levels in Sera of COPD Patients: Potential Implication of the CD200/CD200R Axis in the Disease Course.

Priya Sakthivel, Angele Breithaupt, Marcus Gereke, David A Copland, Christian Schulz, Achim D Gruber, Andrew D Dick, Jens Schreiber, Dunja Bruder

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In one paragraph

Article in Lung, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

6 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

9 authors at 4 institutions in 2 countries.

Priya SakthivelImmune Regulation Group, Helmholtz Centre for Infection Research, Inhoffenstrasse 7, 38124, Braunschweig, Germany. priya.sakthivel@helmholtz-hzi.de.
Angele BreithauptDepartment of Veterinary Medicine, Institute of Veterinary Pathology, Freie Universität Berlin, Berlin, Germany.
Marcus GerekeImmune Regulation Group, Helmholtz Centre for Infection Research, Inhoffenstrasse 7, 38124, Braunschweig, Germany.
David A CoplandSchool of Clinical Sciences, University of Bristol, Bristol, BS8 1TD, UK.
Christian SchulzDepartment of Gastroenterology, Hepatology and Infectious Diseases, Otto-von-Guericke-University Magdeburg, University Hospital, Magdeburg, Germany.
Achim D GruberDepartment of Veterinary Medicine, Institute of Veterinary Pathology, Freie Universität Berlin, Berlin, Germany.
Andrew D DickSchool of Clinical Sciences, University of Bristol, Bristol, BS8 1TD, UK.
Jens SchreiberDepartment of Pulmonology, Otto-von-Guericke-University Magdeburg, University Hospital, Magdeburg, Germany.
Dunja BruderImmune Regulation Group, Helmholtz Centre for Infection Research, Inhoffenstrasse 7, 38124, Braunschweig, Germany.
Otto-von-Guericke University Magdeburg · DEFreie Universität Berlin · DEUniversity of Bristol · GBHelmholtz Centre for Infection Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCOPD represents a multifactorial lung disorder with high morbidity and mortality. Despite intensive research concerning the underlying disease mechanisms, the involvement of the CD200/CD200R axis in supporting or preventing the onset of COPD has not yet been addressed. Since the CD200/CD200R axis is crucially implicated in the maintenance of pulmonary immune homeostasis, we hypothesized that it might be involved in controlling the onset of COPD.

methodsTo address this, we analyzed the serum samples from COPD patients and normal controls for soluble (s) CD200 and correlated the data to COPD-relevant clinical parameters. In addition, basic studies were conducted in CD200-deficient and wild-type mice in which COPD-like inflammation was induced with elastase/LPS followed by lung and serum component analysis.

resultsWe observed a positive correlation between serum sCD200 and IL-6 levels as well as a trend toward a negative correlation of sCD200 with vitamin D3 in COPD patients. Further investigations in mice revealed that despite elevated serum concentration of MMP-9 in CD200KO mice, the early onset of COPD-like lung inflammation was similar in CD200-deficient and wild-type animals in terms of immune cell infiltration, emphysematous changes, and mucus overproduction.

conclusionsWhile our murine studies suggest that the co-inhibitory molecule CD200 does not appear to play a prominent role in the early onset of COPD-like features, correlation of sCD200 serum levels with COPD-related parameters in humans with established disease revealed that the CD200/CD200R axis may be mechanistically linked to the disease course in COPD patients.

Indexed as

AgedAnimalsAntigens, CDAntigens, SurfaceCase-Control StudiesCholecalciferolDisease Models, AnimalFemaleHumansInterleukin-6LipopolysaccharidesLymphocytesMacrophages, AlveolarMaleMatrix Metalloproteinase 9MiceAntigens, CDantigens, CD200Antigens, SurfaceCD200R1 protein, humanCholecalciferolInterleukin-6LipopolysaccharidesMatrix Metalloproteinase 9Mmp9 protein, mouseOrexin ReceptorsPancreatic ElastaseReceptors, Cell SurfaceCD200/CD200R axisCD200-deficient miceCOPDLPS/elastase modelMMP-9

Identifiers

PMID27864635
OpenAlexW2550921293

What OpenQuestion holds

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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.