Evidence map›Paper›PMID 33193355›Full record

ArticleFrontiers in immunology2020

"Age Related Differences in the Biology of Chronic Graft-Versus-Host Disease After Hematopoietic Stem Cell Transplantation".

Geoff D E Cuvelier, Amanda Li, Sibyl Drissler, Amina Kariminia, Sayeh Abdossamadi, Jacob Rozmus, Jean-Pierre Chanoine, Bernard Ng, Sara Mostafavi, Ryan R Brinkman and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
1.9field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 23 citations in OpenAlex.

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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

11 authors at 4 institutions in 1 country.

Geoff D E CuvelierPediatric Blood and Marrow Transplant Program, CancerCare Manitoba, University of Manitoba, Winnipeg, MB, Canada.
Amanda LiMichael Cuccione Childhood Cancer Research Program, British Columbia Children's Hospital, University of British Columbia, Vancouver, BC, Canada.
Sibyl DrisslerTerry Fox Laboratory, BC Cancer, Department of Medical Genetics UBC, Vancouver, BC, Canada.
Amina KariminiaMichael Cuccione Childhood Cancer Research Program, British Columbia Children's Hospital, University of British Columbia, Vancouver, BC, Canada.
Sayeh AbdossamadiMichael Cuccione Childhood Cancer Research Program, British Columbia Children's Hospital, University of British Columbia, Vancouver, BC, Canada.
Jacob RozmusMichael Cuccione Childhood Cancer Research Program, British Columbia Children's Hospital, University of British Columbia, Vancouver, BC, Canada.
Jean-Pierre ChanoineDepartment of Pediatrics, Endocrinology and Diabetes Unit, British Columbia Children's Hospital, Vancouver, BC, Canada.
Bernard NgDepartment of Statistics, Centre for Molecular Medicine and Therapeutics, British Columbia Children's Hospital, University of British Columbia, Vancouver, BC, Canada.
Sara MostafaviDepartment of Statistics, Centre for Molecular Medicine and Therapeutics, British Columbia Children's Hospital, University of British Columbia, Vancouver, BC, Canada.
Ryan R BrinkmanTerry Fox Laboratory, BC Cancer, Department of Medical Genetics UBC, Vancouver, BC, Canada.
Kirk R SchultzMichael Cuccione Childhood Cancer Research Program, British Columbia Children's Hospital, University of British Columbia, Vancouver, BC, Canada.
University of British Columbia · CABC Children's Hospital · CACancerCare Manitoba · CATerry Fox Research Institute · CA

Funding

CIHR
6 · The paper itself

Abstract

It is established that pediatric hematopoietic stem cell transplant (HSCT) recipients have a lower rate of chronic graft-versus-host disease (cGvHD) compared to adults. Our group has previously published immune profiles changes associated with cGvHD of clinically well-defined adult and pediatric HSCT cohorts. Since all analyses were performed by the same research group and analyzed using identical methodology, we first compared our previous immune profile analyses between adults and children. We then performed additional analyses comparing the T cell populations across age groups, and a sub-analysis of the impact of the estimated pubertal status at time of HSCT in our pediatric cohort. In all analyses, we corrected for clinical covariates including total body irradiation and time of onset of cGvHD. Three consistent findings were seen in both children and adults, including elevations of ST2 and naive helper T (Th) cells and depression of NK

Indexed as

Age FactorsHematopoietic Stem Cell TransplantationAdolescentAdultB-LymphocytesChildChronic DiseaseFemaleGraft vs Host DiseaseHumansImmunophenotypingInterleukin-1 Receptor-Like 1 ProteinLymphocyte ActivationMaleMiddle AgedT-Lymphocytes, Helper-InducerIL1RL1 protein, humanInterleukin-1 Receptor-Like 1 Proteinadolescentadultschildrenchronic graft-versus-host diseaseimmune profilepuberty

Identifiers

PMID33193355
PMCPMC7641628
OpenAlexW3093435785

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.