Evidence map›Paper›PMID 30848661›Full record

ArticleAmerican journal of respiratory cell and molecular biology2019

Cystic Fibrosis Plasma Blunts the Immune Response to Bacterial Infection.

Xi Zhang, Amy Pan, Shuang Jia, Justin E Ideozu, Katherine Woods, Kathleen Murkowski, Martin J Hessner, Pippa M Simpson, Hara Levy

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory cell and molecular biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Update in Pediatrics 2020.American journal of respiratory and critical care medicine · 2021
    Article
  8. Transcriptome Sequencing IdentifiesFrontiers in genetics · 2021
    Article
  9. The Multifaceted Roles of MicroRNAs in Cystic Fibrosis.Diagnostics (Basel, Switzerland) · 2020
    Review
  10. Review
  11. Strong toll-like receptor responses in cystic fibrosis patients are associated with higher lung function.Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society · 2020
    Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Cystic Fibrosis Inflammation: Hyperinflammatory, Hypoinflammatory, or Both?American journal of respiratory cell and molecular biology · 2019
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 4 institutions in 1 country.

Xi ZhangDivision of Pulmonary Medicine, Department of Pediatrics, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.ORCID 0000-0003-4766-822X
Amy PanChildren's Research Institute of the Children's Hospital of Wisconsin, Wauwatosa, Wisconsin; and.
Shuang JiaDivision of Endocrinology, Department of Pediatrics.
Justin E IdeozuDivision of Pulmonary Medicine, Department of Pediatrics, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.
Katherine WoodsDivision of Pediatric Critical Care Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Kathleen MurkowskiDivision of Pediatric Critical Care Medicine, Medical College of Wisconsin, Milwaukee, Wisconsin.
Martin J HessnerChildren's Research Institute of the Children's Hospital of Wisconsin, Wauwatosa, Wisconsin; and.
Pippa M SimpsonChildren's Research Institute of the Children's Hospital of Wisconsin, Wauwatosa, Wisconsin; and.
Hara LevyDivision of Pulmonary Medicine, Department of Pediatrics, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois.ORCID 0000-0002-3784-0711
Children's Hospital of Wisconsin · USNorthwestern University · USMedical College of Wisconsin · USPediatrics and Genetics · US

Funding

Integration of Genomics with Genetics - Molecular Phenotypes for CF Lung DiseaseDP2OD007031 · OD · MEDICAL COLLEGE OF WISCONSIN · PI LEVY, HARA · 2010 to 2010
$2.2M
NIH HHS DP2 OD007031
6 · The paper itself

Abstract

Cystic fibrosis (CF) is caused by mutations of the gene encoding the CF transmembrane conductance regulator. It remains unclear whether the abnormal immune response in CF involves extrinsic signals released from the external or internal environment. We sought to characterize the peripheral immune signatures in CF and its association with clinical phenotypes. Healthy peripheral blood mononuclear cells (PBMCs) were cultured with plasma from CF probands (CFPs) or healthy control subjects (HCs) followed by nCounter gene and microRNA (miRNA) profiling. A discovery cohort of 12 CFPs and 12 HCs and a validation cohort of 103 CFPs and 31 HCs (our previous microarray data [GSE71799]) were analyzed to characterize the composition of cultured immune cells and establish a miRNA‒mRNA network. Cell compositions and miRNA profiles were associated with clinical characteristics of the cohorts. Significantly differentially expressed genes and abundance of myeloid cells were downregulated in PMBCs after culture with CF plasma (

Indexed as

Bacterial InfectionsCells, CulturedCystic FibrosisCystic Fibrosis Transmembrane Conductance RegulatorHumansLeukocytes, MononuclearLungMicroRNAsMonocytesPlasmaPseudomonas aeruginosaPseudomonas InfectionsCFTR protein, humanCystic Fibrosis Transmembrane Conductance RegulatorMicroRNAscystic fibrosisgene expressionimmune responsemicroRNAperipheral blood mononuclear cells

Identifiers

PMID30848661
PMCPMC6839930
OpenAlexW2921486742

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.