Evidence map›Paper›PMID 30220008›Full record

ReviewImmunogenetics2019

On the role of the immunoproteasome in transplant rejection.

Michael Basler, Jun Li, Marcus Groettrup

Abstract readReview
PubMed Publisher
In one paragraph

Review in Immunogenetics, 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
–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

16 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. The Significant Role of PA28αβ in CD8International journal of molecular sciences · 2024
    Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
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  12. Review
  13. Review
  14. Article
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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

3 authors.

Michael BaslerDivision of Immunology, Department of Biology, University of Konstanz, P1101 Universitätsstrasse 10, D-78457, Konstanz, Germany. Michael.Basler@uni-konstanz.de.ORCID 0000-0002-9428-2349
Jun LiDivision of Immunology, Department of Biology, University of Konstanz, P1101 Universitätsstrasse 10, D-78457, Konstanz, Germany.
Marcus GroettrupDivision of Immunology, Department of Biology, University of Konstanz, P1101 Universitätsstrasse 10, D-78457, Konstanz, Germany. Marcus.Groettrup@uni-konstanz.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The immunoproteasome is expressed in cells of hematopoietic origin and is induced during inflammation by IFN-γ. Targeting the immunoproteasome with selective inhibitors has been shown to be therapeutically effective in pre-clinical models for autoimmune diseases, colitis-associated cancer formation, and transplantation. Immunoproteasome inhibition prevents activation and proliferation of lymphocytes, lowers MHC class I cell surface expression, reduces the expression of cytokines of activated immune cells, and curtails  T helper 1 and 17 cell differentiation. This might explain the in vivo efficacy of immunoproteasome inhibition in different pre-clinical disease models for autoimmunity, cancer, and transplantation. In this review, we summarize the effect of immunoproteasome inhibition in different animal models for transplantation.

Indexed as

AnimalsAutoimmune DiseasesGraft RejectionHistocompatibility Antigens Class IHumansOrgan TransplantationProteasome Endopeptidase ComplexProteasome InhibitorsSignal TransductionHistocompatibility Antigens Class IProteasome Endopeptidase ComplexProteasome InhibitorsAntigen presentationAntigen processingImmunoproteasomeProteasomeTransplantation

Identifiers

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.