Evidence map›Paper›PMID 36032072›Full record

ArticleFrontiers in immunology2022

M2 Macrophages promote IL-33 expression, ILC2 expansion and mucous metaplasia in response to early life rhinovirus infections.

Mingyuan Han, Haley A Breckenridge, Shiuhyang Kuo, Shilpi Singh, Adam G Goldsmith, Yiran Li, Jordan E Kreger, J Kelley Bentley, Marc B Hershenson

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  3. Group 2 innate lymphoid cells derived IL-9 reduces macrophage apoptosis and attenuates acute lung injury in sepsis.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Article
  4. Review
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  7. Early-life pulmonary viral infection leads to long-term functional and lower airway structural changes in the lungs.American journal of physiology. Lung cellular and molecular physiology · 2024
    Article
  8. Article
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  10. Review
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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

9 authors at 1 institution in 1 country.

Mingyuan HanDepartment of Pediatrics, University of Michigan Medical School, Ann Arbor, MI, United States.
Haley A BreckenridgeDepartment of Pediatrics, University of Michigan Medical School, Ann Arbor, MI, United States.
Shiuhyang KuoDepartment of Pediatrics, University of Michigan Medical School, Ann Arbor, MI, United States.
Shilpi SinghDepartment of Pediatrics, University of Michigan Medical School, Ann Arbor, MI, United States.
Adam G GoldsmithDepartment of Pediatrics, University of Michigan Medical School, Ann Arbor, MI, United States.
Yiran LiDepartment of Pediatrics, University of Michigan Medical School, Ann Arbor, MI, United States.
Jordan E KregerDepartment of Pediatrics, University of Michigan Medical School, Ann Arbor, MI, United States.
J Kelley BentleyDepartment of Pediatrics, University of Michigan Medical School, Ann Arbor, MI, United States.
Marc B HershensonDepartment of Pediatrics, University of Michigan Medical School, Ann Arbor, MI, United States.
University of Michigan–Ann Arbor · US

Funding

Early Life Rhinovirus Infection and Childhood AsthmaR01AI120526 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HERSHENSON, MARC B. · 2016 to 2024
$3.9M
Models of rhinovirus-C respiratory infection and asthmaR01AI155444 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI HERSHENSON, MARC B. · 2020 to 2024
$2.1M
NIAID NIH HHS R01 AI120526NIAID NIH HHS R01 AI155444
6 · The paper itself

Abstract

Wheezing-associated rhinovirus (RV) infections are associated with asthma development. We have shown that infection of immature mice with RV induces type 2 cytokine production and mucous metaplasia which is dependent on IL-33 and type 2 innate lymphoid cells (ILC2s) and intensified by a second heterologous RV infection. We hypothesize that M2a macrophages are required for the exaggerated inflammation and mucous metaplasia in response to heterologous RV infection. Wild-type C57Bl/6J mice and LysM Conclusion: Early-life RV infection alters the macrophage response to subsequent heterologous infection, permitting enhanced IL-33 expression, ILC2 expansion and intensified airway inflammation and mucous metaplasia.

Indexed as

Interleukin-33RhinovirusAnimalsImmunity, InnateInflammationLymphocytesMacrophagesMetaplasiaMiceRNA, MessengerInterleukin-33RNA, MessengerIL-33ILC2M2 macrophageneonateRhinovirus

Identifiers

PMID36032072
PMCPMC9412168
OpenAlexW4291123538

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.