Evidence map›Paper›PMID 42216148›Full record

ArticleBMC microbiology2026

Dysregulated myeloid-T cell immunity in refractory Mycoplasma pneumoniae pneumonia: high inflammation meets T cell suppression.

Yanjuan Yu, Zijie Li, Gaijing Jia, Chunbo Hao, Genhao Wang, Shouhang Chen, Yang Wu, Fang Wang, Yuefei Jin, Yu Tang

Abstract read
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Article in BMC microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Yanjuan Yu *Henan Children's Hospital, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou Children's Hospital, Zhengzhou, 450018, China.
Zijie Li *Department of Epidemiology, College of Public Health, Zhengzhou University, Zhengzhou, 450001, China.
Gaijing JiaHenan Children's Hospital, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou Children's Hospital, Zhengzhou, 450018, China.
Chunbo HaoDepartment of Epidemiology, College of Public Health, Zhengzhou University, Zhengzhou, 450001, China.
Genhao WangDepartment of Epidemiology, College of Public Health, Zhengzhou University, Zhengzhou, 450001, China.
Shouhang ChenHenan Children's Hospital, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou Children's Hospital, Zhengzhou, 450018, China.
Yang WuHenan Children's Hospital, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou Children's Hospital, Zhengzhou, 450018, China.
Fang WangHenan Children's Hospital, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou Children's Hospital, Zhengzhou, 450018, China.
Yuefei JinHenan Children's Hospital, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou Children's Hospital, Zhengzhou, 450018, China. jyf201907@zzu.edu.cn.
Yu TangHenan Children's Hospital, Children's Hospital Affiliated to Zhengzhou University, Zhengzhou Children's Hospital, Zhengzhou, 450018, China. tangyu010312@sina.com.

Funding

China Postdoctoral Science Foundation 2024T170246Open Grant from the Pingyuan Laboratory 2023PY-OP-0202Open Project of Henan Province Engineering Research Center of Diagnosis and Treatment of Pediatric Infection and Critical Care ERC202302Open Project of Key Laboratory of Children's Disease Research in Guangxi's Colleges and Universities GXCDR202401Open Project of Key Laboratory of Infection and Immunity of Anhui Higher Education Institutes I&I-2024-R01Program for Innovative Talents in Higher Education Institutions of Henan Province 25HASTIT055supported by Outstanding Youth Science Foundation of Henan Province 252300421122
6 · The paper itself

Abstract

backgroundAlthough the clinical burden associated with refractory Mycoplasma pneumoniae pneumonia (RMPP) has been continuously increasing in recent years, the immunological mechanisms of RMPP remain poorly understood.

methodsA total of 27 RMPP patients, 24 general Mycoplasma pneumoniae pneumonia (GMPP) patients, and 24 bronchial foreign body patients were enrolled in this study. Protein array technology was used to assess the cytokine profiles in bronchoalveolar lavage fluid (BALF) samples from the patients. Functional interactions among differentially expressed cytokines (DECs) were investigated using protein-protein interaction (PPI) network and pathway enrichment analyses. The impact of DECs on the clinical prognosis and laboratory indicators of the patients was further analyzed in conjunction with clinical data.

resultsSeven DECs were identified: T cell-associated (IL-12p70, IFN-γ, IL-7, IL-4) and myeloid-associated (IL-8, MCP-1, MIP-1β). Compared with GMPP, RMPP BALF showed significantly decreased T cell cytokines and elevated myeloid cytokines. Pathway enrichment analysis revealed these DECs were significantly enriched in the JAK-STAT signaling pathway. ROC analysis suggested that IL-12p70 and IL-4 had the highest discriminative ability among the DECs, but these results are preliminary due to the limited sample size and need external validation. Furthermore, all seven DECs showed correlations with patients' clinical indicators and prognostic parameters.

conclusionsRMPP exhibits a dual immune dysregulation: myeloid hyperinflammation and T cell suppression, with the dysregulated cytokine network converging on JAK-STAT signaling. This provides novel mechanistic insights and identifies potential therapeutic targets.

Indexed as

InflammationMycoplasma pneumoniaeMyeloid CellsPneumonia, MycoplasmaT-LymphocytesAdultBronchoalveolar Lavage FluidCytokinesFemaleHumansMaleMiddle AgedPrognosisProtein Interaction MapsSignal TransductionCytokinesBronchoalveolar lavage fluidCytokine profileRefractory Mycoplasma pneumoniae pneumoniaT Cell Suppression

Identifiers

PMID42216148
PMCPMC13436307

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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.