Evidence map›Paper›PMID 22105417›Full record

ArticleEuropean journal of immunology2012

Decreased NKp46 and NKG2D and elevated PD-1 are associated with altered NK-cell function in pediatric transplant patients with PTLD.

Silke Wiesmayr, Steven A Webber, Camila Macedo, Iulia Popescu, Louise Smith, Jane Luce, Diana Metes

Abstract read
In one paragraph

Article in European journal of immunology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

69 citing papers in PubMed, 102 citations in OpenAlex.

  1. Article
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  8. Article
  9. Review
  10. Article
  11. CD56Annals of hematology · 2024
    Article
  12. Review
  13. Article
  14. Increased PD-1International journal of general medicine · 2024
    Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  20. Review

9 more citing papers are in PubMed but not listed here.

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.

Silke WiesmayrThomas E. Starzl Transplantation Institute, Pittsburgh, PA 15213, USA.
Steven A Webber
Camila Macedo
Iulia Popescu
Louise Smith
Jane Luce
Diana Metes
University of Pittsburgh · USChildren's Hospital of Pittsburgh · US

Funding

Transplant EBV Disease: Pathogenesis and ImmunotherapyP50HL074732 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI WEBBER, STEVEN A. · 2004 to 2008
$12.2M
NHLBI NIH HHS 5P50HL074732NHLBI NIH HHS P50 HL074732
6 · The paper itself

Abstract

Post-transplantation lymphoproliferative disorders (PTLD) are life-threatening complications of organ transplantation caused by EBV infection and the use of chronic immunosuppression. While T-cell impairment is known to play a critical role in the immunopathogenesis of EBV complications post-transplantation, the role of NK cells is still under investigation. Here, we have characterized NK-cell phenotype and function in peripheral blood from asymptomatic pediatric thoracic transplant patients, patients with PTLD, and healthy controls. Overall, asymptomatic pediatric solid organ transplant (Tx) patients presented significant expansion of the CD56(bright) CD16(±) subset and displayed effective NK-cell function, while PTLD patients accumulated CD56(dim) CD16(-) and CD56(-) CD16(+) NK-cell subsets. In addition, NK cells from PTLD patients down-regulated NKp46 and NKG2D, and significantly up-regulated PD-1. These phenotypic changes were associated with NK functional impairment, resembling cellular exhaustion. Disrupting PD-1 inhibitory pathway improved IFN-γ release, but did not enhance cytotoxicity in PTLD patients, suggesting that these defects were partially PD-1 independent. Our results indicate the important role of NK cells during EBV surveillance post-transplantation, with implications for the immunopathogenesis of EBV complications, and suggest that monitoring NK cells in transplant patients may hold clinical value.

Indexed as

Postoperative ComplicationsAdolescentCD56 AntigenCell Growth ProcessesCells, CulturedChildChild, PreschoolCytotoxicity, ImmunologicEpstein-Barr Virus InfectionsFemaleGene Expression RegulationHeart TransplantationHerpesvirus 4, HumanHumansImmunosuppression TherapyInfantCD56 AntigenKLRK1 protein, humanNatural Cytotoxicity Triggering Receptor 1NCR1 protein, humanNK Cell Lectin-Like Receptor Subfamily KPDCD1 protein, humanProgrammed Cell Death 1 Receptor

Identifiers

PMID22105417
PMCPMC3607363
OpenAlexW1511635744

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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.