Evidence map›Paper›PMID 41031886›Full record

ArticleThe Journal of clinical investigation2025

Pharmacological targeting of the IL-17/neutrophil axis attenuates calcific deposits in rat models of calciphylaxis.

Bo Tao, Edward Z Cao, James Hyun, Sivakumar Ramadoss, Juan F Alvarez, Lianjiu Su, Qihao Sun, Zhihao Liu, Linlin Zhang, Alejandro Espinoza and 5 more

Abstract read
In one paragraph

Article in The Journal of clinical investigation, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

15 authors.

Bo TaoDivision of Cardiology, Department of Medicine, David Geffen School of Medicine.
Edward Z CaoDivision of Cardiology, Department of Medicine, David Geffen School of Medicine.
James HyunDivision of Cardiology, Department of Medicine, David Geffen School of Medicine.
Sivakumar RamadossDivision of Cardiology, Department of Medicine, David Geffen School of Medicine.
Juan F AlvarezDivision of Cardiology, Department of Medicine, David Geffen School of Medicine.
Lianjiu SuDivision of Cardiology, Department of Medicine, David Geffen School of Medicine.
Qihao SunDivision of Cardiology, Department of Medicine, David Geffen School of Medicine.
Zhihao LiuDivision of Cardiology, Department of Medicine, David Geffen School of Medicine.
Linlin ZhangDivision of Cardiology, Department of Medicine, David Geffen School of Medicine.
Alejandro EspinozaDepartment of Human Genetics, David Geffen School of Medicine, UCLA, Los Angeles, California, USA.
Yiqian GuDepartment of Molecular, Cell and Developmental Biology, College of Letters and Sciences.
Feiyang MaDepartment of Cell and Developmental Biology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.
Shen LiDivision of Cardiology, Department of Medicine, David Geffen School of Medicine.
Matteo PellegriniDepartment of Molecular, Cell and Developmental Biology, College of Letters and Sciences.
Arjun DebDivision of Cardiology, Department of Medicine, David Geffen School of Medicine.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Calciphylaxis is a rare but life-threatening disorder characterized by ectopic calcification affecting the subcutaneous tissues and blood vessels of the skin. Survival rates are less than a year after diagnosis, and yet despite the severity of the condition, the pathobiology of calciphylaxis is ill understood. Here, we created animal models of calciphylaxis that recapitulated many characteristics of the human phenotype. We demonstrate that cutaneous calcification is preceded by inflammatory cell infiltration. We show that increased local skin inflammation, regardless of the inciting cause, in the presence of hypercalcemia and hyperphosphatemia contributes to cutaneous ectopic calcification. Genetically modified rodents lacking immune activation of T and B cells or NK cells are resistant to developing cutaneous calcification. Consistent with this, administration of the immunosuppressive cyclophosphamide reduced calcific deposits, as did T cell suppression with cyclosporine. We demonstrate that IL-17 is upregulated in calcific skin and neutrophils are the predominant cell type expressing IL-17 and tissue-nonspecific alkaline phosphatase (TNAP) that are necessary for ectopic calcification. Targeting IL-17 with a monoclonal antibody or using a myeloperoxidase inhibitor to blunt neutrophil activation notably attenuated calcific deposits in vivo. Taken together, these observations provide fresh insight into the role of the immune system and the IL-17/neutrophil axis in mediating ectopic calcification in rodent models of calciphylaxis.

Indexed as

CalciphylaxisInterleukin-17NeutrophilsAlkaline PhosphataseAnimalsDisease Models, AnimalHumansMaleMiceRatsRats, Sprague-DawleySkinAlkaline PhosphataseInterleukin-17Bone diseaseCell biologyDermatologyNeutrophilsSkin

Identifiers

PMID41031886
PMCPMC12483568

What OpenQuestion holds

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LicenceCC BY
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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.