Evidence map›Paper›PMID 25726869›Full record

ArticleCellular & molecular immunology2016

Complement 5a receptor-mediated neutrophil dysfunction is associated with a poor outcome in sepsis.

Ruonan Xu, Fang Lin, Chunmei Bao, Huihuang Huang, Chengcheng Ji, Siyu Wang, Lei Jin, Lijian Sun, Ke Li, Zheng Zhang and 1 more

Open access · bronzeAbstract read
In one paragraph

Article in Cellular & molecular immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 18% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Neutrophil activity in sepsis: a systematic review.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2020
    Pooled it
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  17. High levels of circulating GM-CSFCellular & molecular immunology · 2019
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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 1 institution in 1 country.

Ruonan XuResearch Centre for Biological Therapy, The Institute of Translational Hepatology, Beijing 302 Hospital, Beijing, China.
Fang LinThe Institute of Intensive Care Unit, Beijing 302 Hospital, Beijing, China.
Chunmei BaoCentre of Clinical Laboratory Medicine, Beijing 302 Hospital, Beijing, China.
Huihuang HuangThe Institute of Intensive Care Unit, Beijing 302 Hospital, Beijing, China.
Chengcheng JiThe Institute of Intensive Care Unit, Beijing 302 Hospital, Beijing, China.
Siyu WangResearch Centre for Biological Therapy, The Institute of Translational Hepatology, Beijing 302 Hospital, Beijing, China.
Lei JinResearch Centre for Biological Therapy, The Institute of Translational Hepatology, Beijing 302 Hospital, Beijing, China.
Lijian SunThe Institute of Intensive Care Unit, Beijing 302 Hospital, Beijing, China.
Ke LiThe Institute of Intensive Care Unit, Beijing 302 Hospital, Beijing, China.
Zheng ZhangResearch Centre for Biological Therapy, The Institute of Translational Hepatology, Beijing 302 Hospital, Beijing, China.
Fu-Sheng WangResearch Centre for Biological Therapy, The Institute of Translational Hepatology, Beijing 302 Hospital, Beijing, China.
302 Military Hospital of China · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Complement 5a (C5a) has been implicated in the pathogenesis of sepsis by inducing the functional impairment of neutrophils; however, the utility of C5a receptors (C5aRs; C5aR and C5L2) as biomarkers for the management of sepsis is uncertain. This study investigated the dynamic expression of C5aR and C5L2 on neutrophils and their effects on neutrophil function. We found that sepsis patients displayed low expression levels of C5aR and C5L2 on neutrophils compared to healthy and systemic inflammatory response syndrome (SIRS) subjects, and this expression pattern was correlated with disease severity. Additionally, the expression levels of C5aR and C5L2 were associated with the survival of sepsis patients. In vitro, the addition of C5a significantly reduced C5aR and C5L2 expression levels and IL-8 production in neutrophils from sepsis patients. Those findings suggest that the reduced expression of C5aRs was associated with the functional impairment of neutrophils and a poor prognosis for sepsis patients. Overall, these findings may help establish C5aRs expression levels as early markers to predict the severity of sepsis.

Indexed as

AdultAgedBiomarkersCase-Control StudiesComplement C5aFemaleGene Expression RegulationHumansInterleukin-8MaleMiddle AgedNeutrophilsPrimary Cell CulturePrognosisReceptor, Anaphylatoxin C5aReceptors, ChemokineBiomarkersC5AR1 protein, humanC5aR2 protein, humanComplement C5aInterleukin-8Receptor, Anaphylatoxin C5aReceptors, Chemokine

Identifiers

PMID25726869
PMCPMC4711680
OpenAlexW1974987042

What OpenQuestion holds

Textmetadata
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.