Evidence map›Paper›PMID 36211408›Full record

ArticleFrontiers in immunology2022

Proline metabolism reprogramming of trained macrophages induced by early respiratory infection combined with allergen sensitization contributes to development of allergic asthma in childhood of mice.

Hanglin Li, Linyan Ma, Wenjian Li, Boyang Zheng, Junhai Wang, Shunyan Chen, Yang Wang, Fei Ge, Beibei Qin, Xiaoqing Zheng and 2 more

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 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
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  4. Asthma endotypes and theratypes.Chinese medical journal pulmonary and critical care medicine · 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

12 authors at 3 institutions in 1 country.

Hanglin LiDepartment of Immunology, Hebei Medical University, Shijiazhuang, China.
Linyan MaDepartment of Immunology, Hebei Medical University, Shijiazhuang, China.
Wenjian LiDepartment of Immunology, Hebei Medical University, Shijiazhuang, China.
Boyang ZhengDepartment of Immunology, Hebei Medical University, Shijiazhuang, China.
Junhai WangDepartment of Immunology, Hebei Medical University, Shijiazhuang, China.
Shunyan ChenDepartment of Immunology, Hebei Medical University, Shijiazhuang, China.
Yang WangDepartment of Immunology, Hebei Medical University, Shijiazhuang, China.
Fei GeDepartment of Immunology, Hebei Medical University, Shijiazhuang, China.
Beibei QinDepartment of Immunology, Hebei Medical University, Shijiazhuang, China.
Xiaoqing ZhengDepartment of Immunology, Hebei Medical University, Shijiazhuang, China.
Yuqing DengDepartment of Immunology, Hebei Medical University, Shijiazhuang, China.
Ruihong ZengDepartment of Immunology, Hebei Medical University, Shijiazhuang, China.
Hebei Medical University · CNFourth Hospital of Hebei Medical University · CNHospital of Hebei Province · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Infants with respiratory syncytial virus (RSV)-associated bronchiolitis are at increased risk of childhood asthma. Recent studies demonstrated that certain infections induce innate immune memory (also termed trained immunity), especially in macrophages, to respond more strongly to future stimuli with broad specificity, involving in human inflammatory diseases. Metabolic reprogramming increases the capacity of the innate immune cells to respond to a secondary stimulation, is a crucial step for the induction of trained immunity. We hypothesize that specific metabolic reprogramming of lung trained macrophages induced by neonatal respiratory infection is crucial for childhood allergic asthma. Objective: To address the role of metabolic reprogramming in lung trained macrophages induced by respiratory virus infection in allergic asthma. Methods: Neonatal mice were infected and sensitized by the natural rodent pathogen Pneumonia virus of mice (PVM), a mouse equivalent strain of human RSV, combined with ovalbumin (OVA). Lung CD11b Results: PVM infection combined with OVA sensitization in neonatal mice resulted in non-Th2 (Th1/Th17) type allergic asthma following OVA challenge in childhood of mice. Lung CD11b Conclusion: Proline metabolism reprogramming of trained macrophages induced by early respiratory infection combined with allergen sensitization contributes to development of allergic asthma in childhood. Proline metabolism could be a well target for prevention of allergic asthma in childhood.

Indexed as

AsthmaHypersensitivityRespiratory Syncytial Virus InfectionsRespiratory Tract InfectionsAllergensAnimalsHumansMacrophagesMiceMice, Inbred BALB COvalbuminProlineAllergensOvalbuminProlineallergic asthmainnate immune memoryproline metabolism reprogrammingrespiratory virus infectiontrained macrophages

Identifiers

PMID36211408
PMCPMC9533174
OpenAlexW4296739188

What Socratic 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 Socratic graph.