Evidence map›Paper›PMID 32210974›Full record

ArticleFrontiers in immunology2020

Inhibition of CXCR4 and CXCR7 Is Protective in Acute Peritoneal Inflammation.

Kristian-Christos Ngamsri, Christoph Jans, Rizki A Putri, Katharina Schindler, Jutta Gamper-Tsigaras, Claudia Eggstein, David Köhler, Franziska M Konrad

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

15 citing papers in PubMed, 24 citations in OpenAlex.

  1. Inhalable perfluorocarbon RNA nanocapsules overcome biological barriers to treat lung metastases.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Adenosine-mediated immune responses in inflammatory bowel disease.Frontiers in cell and developmental biology · 2024
    Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
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

8 authors at 1 institution in 1 country.

Kristian-Christos NgamsriDepartment of Anesthesiology and Intensive Care Medicine, University Hospital of Tübingen, Tübingen, Germany.
Christoph JansDepartment of Anesthesiology and Intensive Care Medicine, University Hospital of Tübingen, Tübingen, Germany.
Rizki A PutriDepartment of Anesthesiology and Intensive Care Medicine, University Hospital of Tübingen, Tübingen, Germany.
Katharina SchindlerDepartment of Anesthesiology and Intensive Care Medicine, University Hospital of Tübingen, Tübingen, Germany.
Jutta Gamper-TsigarasDepartment of Anesthesiology and Intensive Care Medicine, University Hospital of Tübingen, Tübingen, Germany.
Claudia EggsteinDepartment of Anesthesiology and Intensive Care Medicine, University Hospital of Tübingen, Tübingen, Germany.
David KöhlerDepartment of Anesthesiology and Intensive Care Medicine, University Hospital of Tübingen, Tübingen, Germany.
Franziska M KonradDepartment of Anesthesiology and Intensive Care Medicine, University Hospital of Tübingen, Tübingen, Germany.
University Children's Hospital Tübingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Our previous studies revealed a pivotal role of the chemokine stromal cell-derived factor (SDF)-1 and its receptors CXCR4 and CXCR7 on migratory behavior of polymorphonuclear granulocytes (PMNs) in pulmonary inflammation. Thereby, the SDF-1-CXCR4/CXCR7-axis was linked with adenosine signaling. However, the role of the SDF-1 receptors CXCR4 and CXCR7 in acute inflammatory peritonitis and peritonitis-related sepsis still remained unknown. The presented study provides new insight on the mechanism of a selective inhibition of CXCR4 (AMD3100) and CXCR7 (CCX771) in two models of peritonitis and peritonitis-related sepsis by injection of zymosan and fecal solution. We observed an increased expression of SDF-1, CXCR4, and CXCR7 in peritoneal tissue and various organs during acute inflammatory peritonitis. Selective inhibition of CXCR4 and CXCR7 reduced PMN accumulation in the peritoneal fluid and infiltration of neutrophils in lung and liver tissue in both models. Both inhibitors had no anti-inflammatory effects in A

Indexed as

Acute DiseaseAnimalsBenzylaminesCapillary PermeabilityChemokine CXCL12CyclamsDisease Models, AnimalHumansMiceMice, Inbred C57BLMice, KnockoutNeutrophilsPeritonitisReceptor, Adenosine A2BReceptors, CXCRReceptors, CXCR4BenzylaminesChemokine CXCL12Cmkor1 protein, mouseCxcl12 protein, mouseCXCR4 protein, mouseCyclamsplerixaforReceptor, Adenosine A2BReceptors, CXCRReceptors, CXCR4adenosine receptor A2BneutrophilPMNSDF-1stromal cell-derived factortight junction proteins

Identifiers

PMID32210974
PMCPMC7076176
OpenAlexW3011229542

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.