Evidence map›Paper›PMID 19525985›Full record

ArticleBone marrow transplantation2010

Donor single nucleotide polymorphism in the CCR9 gene affects the incidence of skin GVHD.

Y Inamoto, M Murata, A Katsumi, Y Kuwatsuka, A Tsujimura, Y Ishikawa, K Sugimoto, M Onizuka, S Terakura, T Nishida and 10 more

Abstract read
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 27% 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

14 citing papers in PubMed, 2 syntheses or guidelines pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Enforced gut homing of murine regulatory T cells reduces early graft-versus-host disease severity.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2023
    Article
  5. Article
  6. Dissecting the contribution of single nucleotide polymorphisms inJournal of translational autoimmunity · 2021
    Article
  7. Article
  8. Article
  9. National Institutes of Health Consensus Development Project on Criteria for Clinical Trials in Chronic Graft-versus-Host Disease: III. The 2014 Biomarker Working Group Report.Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation · 2015
    Article
  10. Biologic markers of chronic GVHD.Bone marrow transplantation · 2014
    Review
  11. Review
  12. Article
  13. Biomarkers in chronic graft-versus-host disease.Expert review of hematology · 2011
    Review
  14. 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

20 authors at 1 institution in 1 country.

Y InamotoDepartment of Hematology and Oncology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
M Murata
A Katsumi
Y Kuwatsuka
A Tsujimura
Y Ishikawa
K Sugimoto
M Onizuka
S Terakura
T Nishida
T Kanie
H Taji
H Iida
R Suzuki
A Abe
H Kiyoi
T Matsushita
K Miyamura
Y Kodera
T Naoe
Nagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The interactions between chemokines and their receptors may have an important role in initiating GVHD after allogeneic hematopoietic SCT (allo-HSCT). CCL25 and CCR9 are unique because they are exclusively expressed in epithelial cells and in Peyer's patches of the small intestine. We focused on rs12721497 (G926A), one of the non-synonymous single nucleotide polymorphisms (SNPs) in the CCR9 gene, and analyzed the SNP of donors in 167 consecutive patients who received allo-HSCT from an HLA-identical sibling donor. Genotypes were tested for associations with acute and chronic GVHD in each organ and transplant outcome. Multivariate analyses showed that the genotype 926AG was significantly associated with the incidence of acute stage > or =2 skin GVHD (hazard ratio: 3.2; 95% confidence interval (95% CI): 1.1-9.1; P=0.032) and chronic skin GVHD (hazard ratio: 4.1; 95% CI: 1.1-15; P=0.036), but not with GVHD in other organs or with relapse, non-relapse mortality or OS. To clarify the functional differences between genotypes, each SNP in retroviral vectors was transfected into Jurkat cells. In chemotaxis assays, the 926G transfectant showed greater response to CCL25 than the 926A transfectant. In conclusion, more active homing of CCR9-926AG T cells to Peyer's patches may produce changes in Ag presentation and result in increased incidence of skin GVHD.

Indexed as

AdolescentAdultChemotaxis, LeukocyteFemaleGraft vs Host DiseaseHematopoietic Stem Cell TransplantationHumansIncidenceJurkat CellsMaleMiddle AgedPolymorphism, Single NucleotideReceptors, CCRSkin DiseasesTissue DonorsTreatment OutcomeCC chemokine receptor 9Receptors, CCR

Identifiers

PMID19525985
OpenAlexW1968317106

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.