Evidence map›Paper›PMID 21814172›Full record

ArticleKidney international2011

Acute pyelonephritis and renal scarring are caused by dysfunctional innate immunity in mCxcr2 heterozygous mice.

Majlis Svensson, Manisha Yadav, Bo Holmqvist, Nataliya Lutay, Catharina Svanborg, Gabriela Godaly

Abstract read
In one paragraph

Article in Kidney international, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
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

27 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. The immune mechanisms of the urinary tract against infections.Frontiers in cellular and infection microbiology · 2025
    Review
  5. Experimental Sepsis Models: Advantages and Limitations.The Eurasian journal of medicine · 2023
    Article
  6. Uropathogen and host responses in pyelonephritis.Nature reviews. Nephrology · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Inflammation drives renal scarring in experimental pyelonephritis.American journal of physiology. Renal physiology · 2017
    Article
  16. Current Murine Models of Sepsis.Surgical infections · 2016
    Review
  17. Androgens Enhance Male Urinary Tract Infection Severity in a New Model.Journal of the American Society of Nephrology : JASN · 2016
    Article
  18. Article
  19. Review
  20. CXCL5 drives neutrophil recruitment in TH17-mediated GN.Journal of the American Society of Nephrology : JASN · 2015
    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

6 authors.

Majlis SvenssonDepartment of Microbiology, Immunology and Glycobiology, Institute of Laboratory Medicine, Lund University, Lund, Sweden.
Manisha Yadav
Bo Holmqvist
Nataliya Lutay
Catharina Svanborg
Gabriela Godaly

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The CXCR1 receptor and chemokine CXCL8 (IL-8) support neutrophil-dependent clearance of uropathogenic Escherichia coli from the urinary tract. CXCR1 is reduced in children prone to pyelonephritis, and heterozygous hCXCR1 polymorphisms are more common in this patient group than in healthy individuals, strongly suggesting a disease association. Since murine CXCR2 (mCXCR2) is functionally similar to human CXCR1, we determined effects of gene heterozygosity on the susceptibility to urinary tract infection by infecting heterozygous (mCxcr2(+/-)) mice with uropathogenic Escherichia coli. Clearance of infection and tissue damage were assessed as a function of innate immunity in comparison to that in knockout (mCxcr2(-/-)) and wild-type (mCxcr2(+/+)) mice. Acute sepsis-associated mortality was increased and bacterial clearance drastically impaired in heterozygous compared to wild-type mice. Chemokine and neutrophil responses were delayed along with evidence of neutrophil retention and unresolved kidney inflammation 1 month after infection. This was accompanied by epithelial proliferation and subepithelial fibrosis. The heterozygous phenotype was intermediate, between knockout and wild-type mice, but specific immune cell infiltrates that accompany chronic infection in knockout mice were not found. Hence, the known heterozygous CXCR1 polymorphisms may predispose patients to acute pyelonephritis and urosepsis.

Indexed as

Immunity, InnateAcute DiseaseAnimalsChemokinesDisease Models, AnimalEpithelial CellsEscherichia coliEscherichia coli InfectionsFibrosisGenetic Predisposition to DiseaseHeterozygoteKidneyLymphocytesMiceMice, 129 StrainMice, Inbred BALB CChemokinesReceptors, Interleukin-8B

Identifiers

PMID21814172
PMCPMC3257042

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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.