Evidence map›Paper›PMID 28941323›Full record

ArticleAmerican journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons2018

A critical role for donor-derived IL-22 in cutaneous chronic GVHD.

Kate H Gartlan, Hemamalini Bommiasamy, Katelyn Paz, Andrew N Wilkinson, Mary Owen, Dawn K Reichenbach, Tatjana Banovic, Kimberly Wehner, Faith Buchanan, Antiopi Varelias and 12 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

32 citing papers in PubMed, 49 citations in OpenAlex.

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  18. The Pathophysiology and Treatment of Graft-Frontiers in immunology · 2021
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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

22 authors at 7 institutions in 2 countries.

Kate H GartlanImmunology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.ORCID 0000-0002-0343-1274
Hemamalini BommiasamyLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.
Katelyn PazDepartment of Pediatrics, University of Minnesota Cancer Center, Minneapolis, MN, USA.
Andrew N WilkinsonImmunology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Mary OwenLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.
Dawn K ReichenbachDepartment of Pediatrics, University of Minnesota Cancer Center, Minneapolis, MN, USA.
Tatjana BanovicImmunology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Kimberly WehnerLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.
Faith BuchananLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.
Antiopi VareliasImmunology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Rachel D KunsImmunology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Karshing ChangImmunology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
Yuri FedoriwLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.
Thomas SheaLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.
James CoghillLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.
Michael ZaikenDepartment of Pediatrics, University of Minnesota Cancer Center, Minneapolis, MN, USA.
Maximilian W PlankHunter Medical Research Institute, University of Newcastle, Callaghan, NSW, Australia.
Paul S FosterHunter Medical Research Institute, University of Newcastle, Callaghan, NSW, Australia.
Andrew D CloustonEnvoi Specialist Pathologists, Brisbane, QLD, Australia.
Bruce R BlazarDepartment of Pediatrics, University of Minnesota Cancer Center, Minneapolis, MN, USA.
Jonathan S SerodyLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill, NC, USA.
Geoffrey R HillImmunology Department, QIMR Berghofer Medical Research Institute, Brisbane, QLD, Australia.
University of North Carolina at Chapel Hill · USUniversity of Minnesota · USQIMR Berghofer Medical Research Institute · AUThe University of Queensland · AUHunter Medical Research Institute · AUEnvoi Specialist Pathologists · AURoyal Adelaide Hospital · AU

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI David Darr · 1985 to 2026
$201.5M
Transgenic/KnockoutP01AI056299 · NIAID · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI BLAZAR, BRUCE R · 2003 to 2023
$42.5M
Project 3: Humoral Targets and B Cell Biology in Chronic Graft-vs.-Host DiseaseP01CA142106 · NCI · DANA-FARBER CANCER INST · PI RITZ, JEROME · 2009 to 2019
$17.5M
TRAINING GRANT IN MICROBIOLOGY/CANCER RESEARCHT32CA009138 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Scott M. Dehm · 1985 to 2026
$11.3M
IMMUNOLOGY TRAINING PROGRAMT32AI007313 · NIAID · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Carla Rothlin · 1989 to 2026
$5.7M
T-CELL TARGETING FOR GVHDR01HL056067 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI BLAZAR, BRUCE R · 1995 to 2022
$5.4M
Th1/Th17 Macrophage Interactions in Cutaneous GVHDR01CA166794 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SERODY, JONATHAN S. · 2012 to 2016
$1.5M
NCI NIH HHS P01 CA142106NCI NIH HHS P30 CA016086NCI NIH HHS R01 CA166794NCI NIH HHS T32 CA009138NHLBI NIH HHS R01 HL056067NIAID NIH HHS P01 AI056299NIAID NIH HHS T32 AI007313
6 · The paper itself

Abstract

Graft-versus-host disease (GVHD) is the major cause of nonrelapse morbidity and mortality after allogeneic stem cell transplantation (allo-SCT). Prevention and treatment of GVHD remain inadequate and commonly lead to end-organ dysfunction and opportunistic infection. The role of interleukin (IL)-17 and IL-22 in GVHD remains uncertain, due to an apparent lack of lineage fidelity and variable and contextually determined protective and pathogenic effects. We demonstrate that donor T cell-derived IL-22 significantly exacerbates cutaneous chronic GVHD and that IL-22 is produced by highly inflammatory donor CD4

Indexed as

Tissue DonorsAnimalsChronic DiseaseFemaleGraft vs Host DiseaseHumansInterleukin-17Interleukin-22InterleukinsMiceMice, Inbred BALB CMice, Inbred C57BLPrognosisSkin DiseasesStem Cell TransplantationTransplantation, HomologousInterleukin-17Interleukin-22Interleukinsbasic (laboratory) research/sciencebone marrow/hematopoietic stem cell transplantationbronchiolitis obliterans (BOS)cytokines/cytokine receptorsgraft-versus-host disease (GVHD)immunobiologylymphocyte biology: differentiation/maturationT cell biology

Identifiers

PMID28941323
PMCPMC5866168
OpenAlexW2757048754

What OpenQuestion holds

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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.