Evidence map›Paper›PMID 41439132›Full record

ArticleJournal of inflammation research2025

Age-Specific Cytokine Profiling in Children with

Ying Sun, Lin Tong, Ming Lin, Zuowei Huang, Jing He, Lin Su, Songmin Ying, Zhimin Chen

Abstract read
In one paragraph

Article in Journal of inflammation research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Immune dysregulation inFrontiers in immunology · 2026
    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

8 authors.

Ying Sun *Department of Pulmonology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310000, People's Republic of China.ORCID 0000-0003-3496-1400
Lin Tong *Department of Pulmonology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310000, People's Republic of China.ORCID 0000-0002-4438-2931
Ming LinDepartment of Pulmonology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310000, People's Republic of China.
Zuowei HuangDepartment of Pulmonology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310000, People's Republic of China.
Jing HeDepartment of Pulmonology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310000, People's Republic of China.
Lin SuDepartment of Pulmonology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310000, People's Republic of China.
Songmin YingDepartment of Pharmacy, Center for Regeneration and Aging Medicine, the Fourth Affiliated Hospital of School of Medicine, Yiwu, 322000, People's Republic of China.
Zhimin ChenDepartment of Pulmonology, Children's Hospital, Zhejiang University School of Medicine, Hangzhou, 310000, People's Republic of China.ORCID 0000-0002-5160-7502

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In the wake of COVID-19, a resurgence of Methods: This study retrospectively analyzed serum cytokine levels in 40 healthy children and 87 MPP patients, with additional cytokine profiling of bronchoalveolar lavage fluid (BALF) in severe cases, combining KEGG pathway analysis to investigate age-related immune patterns. SARS-CoV-2 antibody levels were further detected in these MPP patients, followed by Spearman correlation analysis to assess their correlation with cytokines in MPP children. Results: Age-specific cytokine patterns emerged in MPP children. In 0-2 years, cytokines enriched in IL-17, TLR, and TNF pathways were upregulated in MPP groups compared to controls, while in 6-12 years, cytokines enriched in TLR, RLR, and JAK-STAT pathways were downregulated in MPP groups. Serum patterns in 3-5 years resembled those in 0-2 years, but BALF aligned with 6-12 years. SARS-CoV-2 IgG positively correlated with TWEAK, IL-22, IL-16, IL-12p40, CCL7, and CD152 in 0-2 years (P < 0.05), but negatively with CCL13 in 6-12 years (P < 0.01). Conclusion: Overall, the immune pattern in children with MPP is age-specific and severity-dependent. Higher levels of SARS-CoV-2 IgG are associated with a more robust and mature anti-infective immune response in younger MPP patients, while in older children, besides providing immune memory against pathogens, SARS-CoV-2 IgG also appears to plant a landmine of immune exhaustion.

Indexed as

age-specificchildrencytokinesimmune patternsMycoplasma pneumoniaeSARS-CoV-2 antibody

Identifiers

PMID41439132
PMCPMC12719638

What Socratic holds

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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.