Evidence map›Paper›PMID 38168230›Full record

ArticlebioRxiv : the preprint server for biology2023

Macrophages control pathological interferon responses during viral respiratory infection.

Daisy A Hoagland, Patricia Rodríguez-Morales, Alexander O Mann, Shuang Yu, Alicia Lai, Alan Baez Vazquez, Scott D Pope, Jaechul Lim, Shun Li, Xian Zhang and 3 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 2 countries.

Daisy A HoaglandDepartment of Immunology, Harvard Medical School; Boston, MA, USA.ORCID 0000-0002-6781-3079
Patricia Rodríguez-MoralesDepartment of Immunology, Harvard Medical School; Boston, MA, USA.ORCID 0000-0002-2646-4482
Alexander O MannDepartment of Immunology, Harvard Medical School; Boston, MA, USA.ORCID 0000-0002-5927-1396
Shuang YuDepartment of Immunobiology, Yale University School of Medicine; New Haven, CT, USA.
Alicia LaiDepartment of Immunology, Harvard Medical School; Boston, MA, USA.
Alan Baez VazquezDepartment of Immunology, Harvard Medical School; Boston, MA, USA.ORCID 0000-0001-5768-1271
Scott D PopeDepartment of Immunobiology, Yale University School of Medicine; New Haven, CT, USA.ORCID 0000-0002-5243-3639
Jaechul LimDepartment of Immunobiology, Yale University School of Medicine; New Haven, CT, USA.ORCID 0000-0002-6075-2656
Shun LiImmunology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center; New York, NY, USA.
Xian ZhangImmunology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center; New York, NY, USA.
Ming O LiImmunology Program, Sloan Kettering Institute, Memorial Sloan Kettering Cancer Center; New York, NY, USA.
Ruslan MedzhitovDepartment of Immunobiology, Yale University School of Medicine; New Haven, CT, USA.ORCID 0000-0002-7021-2012
Ruth A FranklinDepartment of Immunology, Harvard Medical School; Boston, MA, USA.ORCID 0000-0002-6563-6187
Harvard University · USMemorial Sloan Kettering Cancer Center · USYale University · USHoward Hughes Medical Institute · USNew Generation University College · ET

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
NRSA Training CoreTL1TR002543 · NCATS · HARVARD MEDICAL SCHOOL · PI MICHEL, THOMAS · 2018 to 2022
$3.4M
Macrophage-mediated regulation of inflammation and tissue repairR35GM150816 · NIGMS · HARVARD MEDICAL SCHOOL · PI Ruth A Franklin · 2023 to 2026
$1.9M
NCATS NIH HHS TL1 TR002543NIDDK NIH HHS P30 DK043351NIGMS NIH HHS R35 GM150816
6 · The paper itself

Abstract

Antiviral immune mediators, including interferons and their downstream effectors, are critical for host defense yet can become detrimental when uncontrolled. Here, we identify a macrophage-mediated anti-inflammatory mechanism that limits type I interferon (IFN-I) responses. Specifically, we found that cellular stress and pathogen recognition induce Oncostatin M (OSM) production by macrophages. OSM-deficient mice succumbed to challenge with influenza or a viral mimic due to heightened IFN-I activation. Macrophage-derived OSM restricted excessive IFN-I production by lung epithelial cells following viral stimulation. Furthermore, reconstitution of OSM in the respiratory tract was sufficient to protect mice lacking macrophage-derived OSM against morbidity, indicating the importance of local OSM production. This work reveals a host strategy to dampen inflammation in the lung through the negative regulation of IFN-I by macrophages.

Identifiers

PMID38168230
PMCPMC10760173
OpenAlexW4389870893

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.