Evidence map›Paper›PMID 27694491›Full record

Trial reportJournal of immunology (Baltimore, Md. : 1950)2016

Upregulation of IFN-Inducible and Damage-Response Pathways in Chronic Graft-versus-Host Disease.

Frances T Hakim, Sarfraz Memon, Ping Jin, Matin M Imanguli, Huan Wang, Najibah Rehman, Xiao-Yi Yan, Jeremy Rose, Jacqueline W Mays, Susan Dhamala and 12 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Journal of immunology (Baltimore, Md. : 1950), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 3 pooled it
4.1field-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

45 citing papers in PubMed, 3 syntheses or guidelines pooled it, 58 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

22 authors at 2 institutions in 1 country.

Frances T HakimExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892; hakimf@mail.nih.gov.ORCID 0000-0003-2507-8229
Sarfraz MemonExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0002-0164-9739
Ping JinDepartment of Transfusion Medicine, Clinical Center, National Institutes of Health, Bethesda, MD 20892.
Matin M ImanguliExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Huan WangDepartment of Transfusion Medicine, Clinical Center, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0003-3100-6141
Najibah RehmanExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0003-2718-6784
Xiao-Yi YanExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Jeremy RoseExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Jacqueline W MaysClinical Research Core, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0002-4472-9974
Susan DhamalaExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Veena KapoorExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
William TelfordExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
John DickinsonExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0001-5184-9184
Sean DavisCancer Genetics Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0002-8991-6458
David HalversonExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Haley B NaikDermatology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892; and.ORCID 0000-0003-2760-3904
Kristin BairdPediatric Oncology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0002-1650-8269
Daniel FowlerExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
David StroncekDepartment of Transfusion Medicine, Clinical Center, National Institutes of Health, Bethesda, MD 20892.ORCID 0000-0001-5867-3265
Edward W CowenDermatology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892; and.
Steven Z PavleticExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
Ronald E GressExperimental Transplantation and Immunology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
National Institutes of Health · USNational Institutes of Health Clinical Center · US

Funding

Immunobiology and therapy of oral mucosal and salivary gland chronic graft-versus-host diseaseZIADE000747 · NIDCR · NATIONAL INSTITUTE OF DENTAL & CRANIOFACIAL RESEARCH · PI MAYS, JACQUELINE · 2016 to 2025
$14.9M
Immune reconstitution following autologous and allogeneic stem cell transplantZICBC010934 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI FLOMERFELT, FRANCIS · 2009 to 2022
$10.0M
Chronic graft-versus-host diseaseZIABC011549 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI COWEN, EDWARD · 2014 to 2021
$5.2M
Autophagy regulates airway epithelial cell mucin secretionK08HL131992 · NHLBI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI DICKINSON, JOHN DAVID · 2016 to 2020
$799k
Immune reconstitution following autologous and allogeneic stem cell transplantZ01BC010934 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HAKIM, FRANCES · 2008 to 2008
$701k
Intramural NIH HHS Z01 BC010934Intramural NIH HHS Z99 CA999999NHLBI NIH HHS K08 HL131992
6 · The paper itself

Abstract

Although chronic graft-versus-host disease (CGVHD) is the primary nonrelapse complication of allogeneic transplantation, understanding of its pathogenesis is limited. To identify the main operant pathways across the spectrum of CGVHD, we analyzed gene expression in circulating monocytes, chosen as in situ systemic reporter cells. Microarrays identified two interrelated pathways: 1) IFN-inducible genes, and 2) innate receptors for cellular damage. Corroborating these with multiplex RNA quantitation, we found that multiple IFN-inducible genes (affecting lymphocyte trafficking, differentiation, and Ag presentation) were concurrently upregulated in CGVHD monocytes compared with normal subjects and non-CGVHD control patients. IFN-inducible chemokines were elevated in both lichenoid and sclerotic CGHVD plasma and were linked to CXCR3

Indexed as

AdultAntigen PresentationB-Cell Activating FactorCell DifferentiationCell MovementChemokine CXCL10Chronic DiseaseDEAD Box Protein 58FemaleGraft vs Host DiseaseHumansImmunity, InnateInterferonsMaleMiddle AgedMonocytesB-Cell Activating FactorChemokine CXCL10CXCR3 protein, humanDEAD Box Protein 58InterferonsReceptors, CXCR3Receptors, ImmunologicReceptors, Pattern RecognitionRIGI protein, humanTLR7 protein, humanTNFSF13B protein, humanToll-Like Receptor 7

Identifiers

PMID27694491
PMCPMC5101132
OpenAlexW2529648056

What OpenQuestion holds

Textmetadata
LicenceTDM
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.