Evidence map›Paper›PMID 32384121›Full record

ArticlePloS one2020

Differential gene analysis during the development of obliterative bronchiolitis in a murine orthotopic lung transplantation model: A comprehensive transcriptome-based analysis.

Atsushi Hata, Hidemi Suzuki, Takahiro Nakajima, Taiki Fujiwara, Yuki Shiina, Taisuke Kaiho, Takahide Toyoda, Terunaga Inage, Takamasa Ito, Yuichi Sakairi and 12 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Immune dysfunction in Alzheimer disease.Nature reviews. Neuroscience · 2026
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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 1 institution in 1 country.

Atsushi HataDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.ORCID 0000-0002-9578-683X
Hidemi SuzukiDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Takahiro NakajimaDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Taiki FujiwaraDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Yuki ShiinaDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.ORCID 0000-0003-0040-0816
Taisuke KaihoDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Takahide ToyodaDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Terunaga InageDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Takamasa ItoDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Yuichi SakairiDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Hajime TamuraDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Hironobu WadaDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Yoshito YamadaDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Masako ChiyoDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Keisuke MatsusakaDepartment of Molecular Oncology, Chiba University Graduate School of Medicine, Chiba, Japan.
Masaki FukuyoDepartment of Molecular Oncology, Chiba University Graduate School of Medicine, Chiba, Japan.
Ken-Ichi ShinoharaDepartment of Molecular Oncology, Chiba University Graduate School of Medicine, Chiba, Japan.
Sakae ItogaDepartment of Laboratory Medicine & Division of Clinical Genetics and Proteomics, Chiba University Graduate School of Medicine, Chiba, Japan.
Shinichiro MotohashiDepartment of Medical Immunology, Chiba University Graduate School of Medicine, Chiba, Japan.
Kazuyuki MatsushitaDepartment of Laboratory Medicine & Division of Clinical Genetics and Proteomics, Chiba University Graduate School of Medicine, Chiba, Japan.
Atsushi KanedaDepartment of Molecular Oncology, Chiba University Graduate School of Medicine, Chiba, Japan.
Ichiro YoshinoDepartment of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan.
Chiba University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundObliterative bronchiolitis (OB) is a known issue during minor histocompatibility antigen (mHA) disparity during lung transplantation. This study evaluated gene expression in a murine orthotropic lung transplantation model using microarray analysis.

methodsLeft lungs from C57BL/10(H-2b) donor mice were transplanted into mHA-mismatched C57BL/6(H-2b) recipient mice. Three groups (OB, non-OB, and sham controls) were confirmed pathologically and analyzed. Gene expression changes in the lung grafts were determined by microarray and immunohistochemical staining, and genes were verified by quantitative PCR in the lungs and mediastinal lymph nodes (LNs).

resultsA total of 1343 genes were upregulated in the OB lungs compared to the sham group. Significant upregulation was observed for genes related to innate, e.g. Tlr2 and CCL3 and adaptive immunity, e.g. H2-ab1 and Il-21. Positive labeling for MHC class II antigen was observed in the bronchial epithelium of OB accompanied with B cells. We found increased Tlr2, Ccl3, H2-ab1, Il-21, Ighg3, Ifng, and Pdcd1 mRNA expression in the OB lung, and increased Il-21, Ighg3, and Pdcd1 expression in the OB LNs.

conclusionsAdaptive and innate immune reactions were involved in OB after lung transplantation, and genetic examination of related genes could be used for detection of OB.

Indexed as

Lung TransplantationAdaptive ImmunityAnimalsBronchiolitisDisease Models, AnimalGene ExpressionGene Expression ProfilingImmunity, InnateLungLymph NodesMaleMice, Inbred C57BLMinor Histocompatibility AntigensRNA, MessengerSpecific Pathogen-Free OrganismsSpleenMinor Histocompatibility AntigensRNA, Messenger

Identifiers

PMID32384121
PMCPMC7209239
OpenAlexW3023828268

What OpenQuestion holds

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Registered trials

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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.