Evidence map›Paper›PMID 37978185›Full record

ArticleNature communications2023

The transcriptional and phenotypic characteristics that define alveolar macrophage subsets in acute hypoxemic respiratory failure.

Eric D Morrell, Sarah E Holton, Matthew Lawrance, Marika Orlov, Zoie Franklin, Mallorie A Mitchem, Hannah DeBerg, Vivian H Gersuk, Ashley Garay, Elizabeth Barnes and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

16 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Immunology of Sepsis.Clinics in chest medicine · 2026
    Review
  5. Article
  6. Article
  7. Monocyte-Derived LGMNResearch (Washington, D.C.) · 2026
    Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Macrophage Dysfunction in Respiratory Disease.Results and problems in cell differentiation · 2024
    Review
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

16 authors at 6 institutions in 2 countries.

Eric D Morrell *Division of Pulmonary, Critical Care, and Sleep Medicine, University of Washington, Seattle, WA, USA. edmorrel@uw.edu.ORCID 0000-0001-9900-3604
Sarah E Holton *Division of Pulmonary, Critical Care, and Sleep Medicine, University of Washington, Seattle, WA, USA.ORCID 0000-0002-6373-3768
Matthew LawranceTranslational Immunology, Benaroya Research Institute, Seattle, WA, USA.
Marika OrlovDivision of Pulmonary Sciences and Critical Care Medicine, University of Colorado, Aurora, CO, USA.ORCID 0000-0003-1961-0813
Zoie FranklinTranslational Immunology, Benaroya Research Institute, Seattle, WA, USA.
Mallorie A MitchemTranslational Immunology, Benaroya Research Institute, Seattle, WA, USA.
Hannah DeBergTranslational Immunology, Benaroya Research Institute, Seattle, WA, USA.
Vivian H GersukTranslational Immunology, Benaroya Research Institute, Seattle, WA, USA.ORCID 0000-0003-4123-9926
Ashley GarayDivision of Pulmonary, Critical Care, and Sleep Medicine, University of Washington, Seattle, WA, USA.
Elizabeth BarnesDivision of Pulmonary, Critical Care, and Sleep Medicine, University of Washington, Seattle, WA, USA.
Ted LiuDivision of Pulmonary, Critical Care, and Sleep Medicine, University of Washington, Seattle, WA, USA.
Ithan D PeltanDivision of Pulmonary and Critical Care Medicine, Intermountain Health, Murray, UT, USA.
Angela RogersDivision of Pulmonary and Critical Care, Stanford University, Stanford, CA, USA.ORCID 0000-0001-6969-6200
Steven ZieglerTranslational Immunology, Benaroya Research Institute, Seattle, WA, USA.ORCID 0000-0003-0657-5529
Mark M WurfelDivision of Pulmonary, Critical Care, and Sleep Medicine, University of Washington, Seattle, WA, USA.
Carmen MikacenicTranslational Immunology, Benaroya Research Institute, Seattle, WA, USA. cmikacenic@benaroyaresearch.org.ORCID 0000-0001-8966-5161
Benaroya Research InstituteUniversity of Washington · USCGIAR · FRIntermountain Healthcare · USStanford University · USUniversity of Colorado Anschutz Medical Campus · US

Funding

Technology Development Project - Increasing the complexity of ex vivo human airway models for studying immune response to viral infectionU19AI142733 · NIAID · JACKSON LABORATORY · PI Damien Chaussabel · 2019 to 2026
$23.1M
RESPIRATORY RESEARCH TRAINING PROGRAMT32HL007287 · NHLBI · UNIVERSITY OF WASHINGTON · PI Kristina Anne Crothers, David J. Horne · 1985 to 2026
$16.7M
Immune Checkpoints in Acute Respiratory Distress Syndrome (IC-ARDS)R01HL149676 · NHLBI · BENAROYA RESEARCH INST AT VIRGINIA MASON · PI MIKACENIC, CARMEN R · 2020 to 2024
$3.0M
The Role of Alveolar Mononuclear Phagocytes in Acute Respiratory Distress SyndromeK23HL144916 · NHLBI · UNIVERSITY OF WASHINGTON · PI MORRELL, ERIC DOUGLAS · 2019 to 2023
$951k
NHLBI NIH HHS K23 HL144916NHLBI NIH HHS R01 HL149676NHLBI NIH HHS T32 HL007287NIAID NIH HHS U19 AI142733
6 · The paper itself

Abstract

The transcriptional and phenotypic characteristics that define alveolar monocyte and macrophage subsets in acute hypoxemic respiratory failure (AHRF) are poorly understood. Here, we apply CITE-seq (single-cell RNA-sequencing and cell-surface protein quantification) to bronchoalveolar lavage and blood specimens longitudinally collected from participants with AHRF to identify alveolar myeloid subsets, and then validate their identity in an external cohort using flow cytometry. We identify alveolar myeloid subsets with transcriptional profiles that differ from other lung diseases as well as several subsets with similar transcriptional profiles as reported in healthy participants (Metallothionein) or patients with COVID-19 (CD163/LGMN). We use information from CITE-seq to determine cell-surface proteins that distinguish transcriptional subsets (CD14, CD163, CD123, CD71, CD48, CD86 and CD44). In the external cohort, we find a higher proportion of CD163/LGMN alveolar macrophages are associated with mortality in AHRF. We report a parsimonious set of cell-surface proteins that distinguish alveolar myeloid subsets using scalable approaches that can be applied to clinical cohorts.

Indexed as

Lung DiseasesRespiratory InsufficiencyHumansMacrophagesMacrophages, AlveolarMonocytes

Identifiers

PMID37978185
PMCPMC10656558
OpenAlexW4388774942

What OpenQuestion holds

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LicenceCC BY
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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.