Evidence map›Paper›PMID 26992230›Full record

ArticleOncotarget2016

Reduced serpinB9-mediated caspase-1 inhibition can contribute to autoinflammatory disease.

Robert van der Burgh, Jan Meeldijk, Lieneke Jongeneel, Joost Frenkel, Niels Bovenschen, Mariëlle van Gijn, Marianne Boes

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. 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
0.9field-weighted citation impact, top 24% 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, 20 citations in OpenAlex.

  1. Article
  2. Comprehensive Analysis of Immune Infiltration and Key Genes in Peri-Implantitis Using Bioinformatics and Molecular Biology Approaches.Medical science monitor : international medical journal of experimental and clinical research · 2024
    Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Serpin B9 controls tumor cell killing by CAR T cells.Journal for immunotherapy of cancer · 2023
    Article
  8. LncRNA SERPINB9P1 expression and polymorphisms are associated with ischemic stroke in a Chinese Han population.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Article
  9. Observational
  10. Article
  11. Article
  12. Article
  13. Article
  14. Genome-wide DNA methylome alterations in acute coronary syndrome.International journal of molecular medicine · 2018
    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

7 authors at 2 institutions in 1 country.

Robert van der BurghDepartment of Pediatric Immunology, Wilhelmina Children's Hospital, UMC Utrecht, EA, Utrecht, Netherlands.
Jan MeeldijkDepartment of Pathology, University Medical Center Utrecht, CX, Utrecht, Netherlands.
Lieneke JongeneelDepartment of Pediatric Immunology, Wilhelmina Children's Hospital, UMC Utrecht, EA, Utrecht, Netherlands.
Joost FrenkelDepartment of General Pediatrics, Wilhelmina Children's Hospital, UMC Utrecht, EA, Utrecht, Netherlands.
Niels BovenschenDepartment of Pathology, University Medical Center Utrecht, CX, Utrecht, Netherlands.
Mariëlle van GijnDepartment of Genetics, University Medical Center Utrecht, EA, Utrecht, Netherlands.
Marianne BoesDepartment of Pediatric Immunology, Wilhelmina Children's Hospital, UMC Utrecht, EA, Utrecht, Netherlands.
University Medical Center Utrecht · NLWilhelmina Children's Hospital · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients who suffer from autoinflammatory disease (AID) exhibit seemingly uncontrolled release of interleukin (IL)-1β. The presence of this inflammatory cytokine triggers immune activation in absence of pathogens and foreign material. The mechanisms that contribute to 'sterile inflammation' episodes in AID patients are not fully understood, although for some AIDs underlying genetic causes have been identified. We show that the serine protease inhibitor B9 (serpinB9) regulates IL-1β release in human monocytes. SerpinB9 function is more commonly known for its role in control of granzyme B. SerpinB9 however also serves to restrain IL-1β maturation through caspase-1 inhibition. We here describe an autoinflammatory disease-associated serpinB9 (c.985G>T, A329S) variant, which we discovered in a patient with unknown AID. Using patient cells and serpinB9 overexpressing monocytic cells, we show the A329S variant of serpinB9 exhibits unobstructed granzyme B inhibition, but compromised caspase-1 inhibition. SerpinB9 gene variants might contribute to AID development.

Indexed as

AdultAmino Acid SequenceAutoimmune DiseasesBase SequenceCaspase 1Cell Line, TumorChildFamily HealthFemaleHumansInflammationInterleukin-1betaMaleMonocytesMutationSequence Homology, Amino AcidCaspase 1Interleukin-1betaSERPINB9 protein, humanSerpinsautoinflammationcaspase-1granzyme BImmune responseImmunityImmunology and Microbiology Sectioninterleukin 1βserpinB9

Identifiers

PMID26992230
PMCPMC4991381
OpenAlexW2327877143

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.