Evidence map›Paper›PMID 23539759›Full record

ArticleJournal of the American Society of Nephrology : JASN2013

MICA variant promotes allosensitization after kidney transplantation.

Pierre Tonnerre, Nathalie Gérard, Mathias Chatelais, Caroline Poli, Stéphanie Allard, Sylvie Cury, Céline Bressollette, Anne Cesbron-Gautier, Béatrice Charreau

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the American Society of Nephrology : JASN, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 37 citations in OpenAlex.

  1. Trial
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  9. A Valine Mismatch at Position 129 ofInternational journal of molecular sciences · 2018
    Article
  10. Review
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  12. Review
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  14. Genetic barriers in transplantation medicine.World journal of transplantation · 2016
    Review
  15. Article
  16. Article
  17. MICA SNPs and the NKG2D system in virus-induced HCC.Journal of gastroenterology · 2015
    Review
  18. Review
  19. 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

9 authors at 5 institutions in 1 country.

Pierre TonnerreCentre de Recherche en Transplantation et Immunologie, LabEx Transplantex, Nantes, France.
Nathalie Gérard
Mathias Chatelais
Caroline Poli
Stéphanie Allard
Sylvie Cury
Céline Bressollette
Anne Cesbron-Gautier
Béatrice Charreau
Établissement Français du Sang · FRInstitut de Transplantation Urologie en Nephrologie · FRCentre Hospitalier Universitaire de Nantes · FRNantes Université · FRUniversité Nantes Angers Le Mans · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MHC class I-related chain A (MICA) antigens are surface glycoproteins strongly implicated in innate immunity, and the MICA gene is highly polymorphic. Clinical observations suggest a role for donor MICA antigens expressed on transplant endothelial cells in the alloimmune response, but the effect of MICA genotype is not well understood. Here, we investigated the immunologic effect of the A5.1 mutation, related to the common MICA*008 allele. Compared with wild-type endothelial cells (ECs), homozygosity for MICA A5.1 associated with an endothelial phenotype characterized by 7- to 10-fold higher levels of MICA mRNA and MICA proteins at the cell surface, as well as exclusive release in exosomes instead of enzymatic cleavage. Mechanistically, we did not detect quantitative changes in regulatory microRNAs. Functionally, A5.1 ECs enhanced NKG2D interaction and natural killer cell activation, promoting NKG2D-dependent lysis of ECs. In kidney transplant recipients, polyreactive anti-MICA sera bound preferentially to ECs from MICA A5.1 donors, suggesting that MICA*008(A5.1) molecules are the preferential antigenic determinants on ECs of grafts. Furthermore, the incidence of MICA A5.1 mismatch revealed a statistically significant association between donor MICA A5.1 and both anti-MICA sensitization and increased proteinuria in kidney recipients. Taken together, these results identify the A5.1 mutation as an immunodominant factor and a potential risk factor for transplant survival.

Indexed as

AdultAgedEndothelial CellsFemaleGenetic Predisposition to DiseaseGenetic VariationGenotypeGraft RejectionHistocompatibility Antigens Class IHumansImmunity, InnateIsoantigensKidney TransplantationMaleMiddle AgedNK Cell Lectin-Like Receptor Subfamily KHistocompatibility Antigens Class IIsoantigensKLRK1 protein, humanMHC class I-related chain ANK Cell Lectin-Like Receptor Subfamily KRNA, Small InterferingSTAT1 Transcription Factor

Identifiers

PMID23539759
PMCPMC3665393
OpenAlexW2139763899

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.