Evidence map›Paper›PMID 30228128›Full record

ArticleBlood advances2018

Impaired bone marrow B-cell development in mice with a bronchiolitis obliterans model of cGVHD.

Oleg V Kolupaev, Trisha A Dant, Hemamalini Bommiasamy, Danny W Bruce, Kenneth A Fowler, Stephen L Tilley, Karen P McKinnon, Stefanie Sarantopoulos, Bruce R Blazar, James M Coghill and 1 more

Open access · goldAbstract read
In one paragraph

Article in Blood advances, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-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

14 citing papers in PubMed, 18 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 2 countries.

Oleg V KolupaevUNC Lineberger Comprehensive Cancer Center.
Trisha A DantDepartment of Microbiology and Immunology, and.
Hemamalini BommiasamyUNC Lineberger Comprehensive Cancer Center.
Danny W BruceUNC Lineberger Comprehensive Cancer Center.
Kenneth A FowlerUNC Lineberger Comprehensive Cancer Center.
Stephen L TilleyDepartment of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Karen P McKinnonUNC Lineberger Comprehensive Cancer Center.
Stefanie SarantopoulosDivision of Hematologic Malignancies and Cellular Therapy, Duke Cancer Institute, Duke University, Durham, NС; and.
Bruce R BlazarMasonic Cancer Center, Minneapolis, MN.
James M CoghillUNC Lineberger Comprehensive Cancer Center.
Jonathan S SerodyUNC Lineberger Comprehensive Cancer Center.
UNC Lineberger Comprehensive Cancer CenterDuke University · USMasonic Cancer CenterUniversity of North Carolina at Chapel Hill · US

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
Pathological B Cells: Novel Strategies to Prevent and Treat Chronic GVHDR01HL129061 · NHLBI · DUKE UNIVERSITY · PI Stefanie Sarantopoulos · 2015 to 2026
$7.7M
Enhancing Treg Therapeutic Efficacy in GVHDR01HL118979 · NHLBI · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, HIPPEN, KELI L · 2014 to 2025
$6.7M
Mechanistic Evaluations of ILC2 Cells for the Treatment/Prevention of GVHDR01HL139730 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SERODY, JONATHAN S. · 2017 to 2020
$2.2M
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 CA166794NHLBI NIH HHS R01 HL118979NHLBI NIH HHS R01 HL129061NHLBI NIH HHS R01 HL139730NIAID NIH HHS P01 AI056299
6 · The paper itself

Abstract

Chronic graft-versus-host disease (cGVHD) causes significant morbidity and mortality in patients after allogeneic bone marrow (BM) or stem cell transplantation (allo-SCT). Recent work has indicated that both T and B lymphocytes play an important role in the pathophysiology of cGVHD. Previously, our group showed a critical role for the germinal center response in the function of B cells using a bronchiolitis obliterans (BO) model of cGVHD. Here, we demonstrated for the first time that cGVHD is associated with severe defects in the generation of BM B lymphoid and uncommitted common lymphoid progenitor cells. We found an increase in the number of donor CD4

Indexed as

Cell DifferentiationAnimalsBiomarkersB-LymphocytesBone Marrow CellsBronchiolitis ObliteransChronic DiseaseCytokinesDisease Models, AnimalGene ExpressionGraft vs Host DiseaseImmunophenotypingLymphocyte DepletionMiceMice, TransgenicOsteoblastsBiomarkersCytokines

Identifiers

PMID30228128
PMCPMC6156893
OpenAlexW2890405528

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.