Evidence map›Paper›PMID 29878854›Full record

ArticleAmerican journal of respiratory and critical care medicine2018

Lung Dysbiosis, Inflammation, and Injury in Hematopoietic Cell Transplantation.

David N O'Dwyer, Xiaofeng Zhou, Carol A Wilke, Meng Xia, Nicole R Falkowski, Katy C Norman, Kelly B Arnold, Gary B Huffnagle, Susan Murray, John R Erb-Downward and 3 more

Open access · greenAbstract read
In one paragraph

Article in American journal of respiratory and critical care medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 4% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 61 citations in OpenAlex.

  1. Guideline
  2. Review
  3. Targeted lungScience advances · 2026
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  7. Genome sequence ofMicrobiology resource announcements · 2024
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  11. How to Understand a Revolution: Guts, Lungs, and Bronchiectasis.American journal of respiratory and critical care medicine · 2023
    Article
  12. The dynamic lung microbiome in health and disease.Nature reviews. Microbiology · 2023
    Review
  13. Review
  14. Review
  15. Article
  16. Observational
  17. Article
  18. Review
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 2 countries.

David N O'Dwyer1 Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine.ORCID 0000-0003-3214-380X
Xiaofeng Zhou1 Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine.
Carol A Wilke1 Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine.
Meng Xia2 Department of Biostatistics, School of Public Health, and.
Nicole R Falkowski1 Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine.
Katy C Norman3 Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan; and.
Kelly B Arnold3 Department of Biomedical Engineering, University of Michigan, Ann Arbor, Michigan; and.
Gary B Huffnagle1 Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine.
Susan Murray2 Department of Biostatistics, School of Public Health, and.
John R Erb-Downward1 Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine.
Gregory A Yanik5 Department of Pediatrics, University of Michigan Medical School, Ann Arbor, Michigan.
Bethany B Moore1 Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine.ORCID 0000-0003-3051-745X
Robert P Dickson1 Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine.ORCID 0000-0002-6875-4277
Pulmonary and Critical Care Associates · USUniversity of Michigan · USCancer Research And Biostatistics · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
Immunobiology of Lung Injury and FibrosisR35HL144481 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOORE, BETHANY B. · 2019 to 2024
$5.2M
Functional Analysis of the Pulmonary Microbiome during COPDR01HL121774 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HUFFNAGLE, GARY B · 2017 to 2020
$3.1M
miR-29b and autophagy regulate alveolar macrophage function post-BMTR01AI117229 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOORE, BETHANY B. · 2015 to 2019
$2.2M
HSCT-induced alterations in DCs to promote IL-17 and lung pathologyR01HL127805 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOORE, BETHANY B. · 2016 to 2018
$1.5M
The Role of the Microbiome in the Acute Respiratory Distress SyndromeK23HL130641 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DICKSON, ROBERT PICKETT · 2016 to 2020
$859k
Toll-like receptors and respiratory microbiota interactions in idiopathic pulmonary fibrosisK99HL139996 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI O'DWYER, DAVID NOEL · 2018 to 2019
$265k
NCI NIH HHS P30 CA046592NHLBI NIH HHS K23 HL130641NHLBI NIH HHS K99 HL139996NHLBI NIH HHS R01 HL121774NHLBI NIH HHS R01 HL127805NHLBI NIH HHS R35 HL144481NIAID NIH HHS R01 AI117229
6 · The paper itself

Abstract

rationaleHematopoietic cell transplant (HCT) is a common treatment for hematological neoplasms and autoimmune disorders. Among HCT recipients, pulmonary complications are common, morbid, and/or lethal, and they have recently been associated with gut dysbiosis. The role of lung microbiota in post-HCT pulmonary complications is unknown.

objectivesTo investigate the role of lung microbiota in post-HCT pulmonary complications using animal modeling and human BAL fluid.

methodsFor animal modeling, we used an established murine model of HCT with and without postengraftment herpes virus infection. For human studies, we characterized lung microbiota in BAL fluid from 43 HCT recipients. Lung bacteria were characterized using 16S ribosomal RNA gene sequencing and were compared with lung histology (murine) and with alveolar inflammation and pulmonary function testing (human). MEASUREMENTS AND MAIN

resultsBoth HCT and viral infection independently altered the composition of murine lung microbiota, but they had no effect on lung microbial diversity. By contrast, combined HCT and viral infection profoundly altered lung microbiota, decreasing community diversity with an associated pneumonitis. Among human HCT recipients, increased relative abundance of the Proteobacteria phylum was associated with impaired pulmonary function, and lung microbiota were significantly associated with alveolar concentrations of inflammatory cytokines.

conclusionsIn animal models and human subjects, lung dysbiosis is a prominent feature of HCT. Lung dysbiosis is correlated with histologic, immunologic, and physiologic features of post-HCT pulmonary complications. Our findings suggest the lung microbiome may be an unappreciated target for the prevention and treatment of post-HCT pulmonary complications.

Indexed as

AnimalsComorbidityDisease Models, AnimalDysbiosisFemaleGastrointestinal MicrobiomeHematopoietic Stem Cell TransplantationHumansInflammationLungLung DiseasesMaleMiceMiddle AgedPostoperative Complicationshematopoietic stem cell transplantationmicrobiomemicrobiotamurine herpes viruspulmonary complications

Identifiers

PMID29878854
PMCPMC6290939
OpenAlexW2807142192

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.