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Mycoplasma pneumoniae CARDS Toxin Exacerbates Ovalbumin-Induced Asthma-Like Inflammation in BALB/c Mice
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1016/j.anai.2013.01.022openalex-snapshot
Mycoplasma pneumoniae in children with acute and refractory asthma
inferredcites →https://doi.org/10.1016/j.jaci.2009.10.047openalex-snapshot
Asthma: Clinical expression and molecular mechanisms
inferredcites →https://doi.org/10.1037/h0031619openalex-snapshot
Measuring nominal scale agreement among many raters.
inferredcites →https://doi.org/10.1038/cmi.2010.31openalex-snapshot
Murine lung eosinophil activation and chemokine production in allergic airway inflammation
inferredcites →https://doi.org/10.1038/nri3341openalex-snapshot
Eosinophils: changing perspectives in health and disease
inferredcites →https://doi.org/10.1056/nejmoa0805435openalex-snapshot
Mepolizumab for Prednisone-Dependent Asthma with Sputum Eosinophilia
inferredcites →https://doi.org/10.1056/nejmoa0808991openalex-snapshot
Mepolizumab and Exacerbations of Refractory Eosinophilic Asthma
inferredcites →https://doi.org/10.1067/mai.2001.113563openalex-snapshot
A link between chronic asthma and chronic infection
inferredcites →https://doi.org/10.1073/pnas.0510644103openalex-snapshot
ADP-ribosylating and vacuolating cytotoxin of Mycoplasma pneumoniae represents unique virulence determinant among bacterial pathogens
inferredcites →https://doi.org/10.1074/jbc.m406037200openalex-snapshot
Identification of a Cooperative Mechanism Involving Interleukin-13 and Eotaxin-2 in Experimental Allergic Lung Inflammation
inferredcites →https://doi.org/10.1084/jem.20071840openalex-snapshot
Allergic pulmonary inflammation in mice is dependent on eosinophil-induced recruitment of effector T cells
inferredcites →https://doi.org/10.1086/392498openalex-snapshot
Mycoplasma pneumoniae and Asthma in Children
inferredcites →https://doi.org/10.1097/00003246-198409000-00017openalex-snapshot
High-frequency ventilation compared to conventional positive-pressure ventilation in the treatment of hyaline membrane disease in primates
inferredcites →https://doi.org/10.1111/j.1365-2222.2009.03309.xopenalex-snapshot
A low dose of Mycoplasma pneumoniae infection enhances an established allergic inflammation in mice: the role of the prostaglandin E2 pathway
inferredcites →https://doi.org/10.1111/j.1365-2958.2010.07092.xopenalex-snapshot
Mycoplasma pneumoniae Community Acquired Respiratory Distress Syndrome toxin expression reveals growth phase and infection‐dependent regulation
inferredcites →https://doi.org/10.1111/j.1574-6976.2008.00129.xopenalex-snapshot
Epidemiology, clinical manifestations, pathogenesis and laboratory detection ofMycoplasma pneumoniaeinfections: Figure 1
inferredcites →https://doi.org/10.1128/cmr.17.4.697-728.2004openalex-snapshot
Mycoplasma pneumoniae and Its Role as a Human Pathogen
inferredcites →https://doi.org/10.1128/iai.00403-06openalex-snapshot
Delayed Inflammatory Response to Primary Pneumonic Plague Occurs in Both Outbred and Inbred Mice
inferredcites →https://doi.org/10.1128/iai.70.2.649-654.2002openalex-snapshot
Mycoplasma pneumoniae Induces Chronic Respiratory Infection, Airway Hyperreactivity, and Pulmonary Inflammation: a Murine Model of Infection-Associated Chronic Reactive Airway Disease
inferredcites →https://doi.org/10.1128/iai.71.3.1520-1526.2003openalex-snapshot
Effects of Respiratory Mycoplasma pneumoniae Infection on Allergen-Induced Bronchial Hyperresponsiveness and Lung Inflammation in Mice
inferredcites →https://doi.org/10.1128/iai.73.5.2828-2834.2005openalex-snapshot
Identification and Characterization of Human Surfactant Protein A Binding Protein ofMycoplasma pneumoniae
inferredcites →https://doi.org/10.1152/ajplung.00167.2004openalex-snapshot
Mycoplasma pneumoniaeinfection increases airway collagen deposition in a murine model of allergic airway inflammation
inferredcites →https://doi.org/10.1164/ajrccm.158.3.9711092openalex-snapshot
Detection of Mycoplasma pneumoniae in the Airways of Adults with Chronic Asthma
inferredcites →https://doi.org/10.1164/rccm.200209-996ocopenalex-snapshot
Atypical Pathogen Infection in Adults with Acute Exacerbation of Bronchial Asthma
inferredcites →https://doi.org/10.1164/rccm.200412-1743ppopenalex-snapshot
Chlamydophila pneumoniae and Mycoplasma pneumoniae
inferredcites →https://doi.org/10.1164/rccm.200709-1387ocopenalex-snapshot
Toll-like Receptor 2 Down-regulation in Established Mouse Allergic Lungs Contributes to Decreased Mycoplasma Clearance
inferredcites →https://doi.org/10.1164/rccm.201001-0080ocopenalex-snapshot
Variation in Colonization, ADP-Ribosylating and Vacuolating Cytotoxin, and Pulmonary Disease Severity among Mycoplasma pneumoniae Strains
inferredcites →https://doi.org/10.1164/rccm.201203-0476ocopenalex-snapshot
Asthmatic Granulomatosis: A Novel Disease with Asthmatic and Granulomatous Features
inferredcites →https://doi.org/10.1165/ajrcmb.24.5.4315openalex-snapshot
Airway Inflammation and Bronchial Hyperresponsiveness after Mycoplasma pneumoniae Infection in a Murine Model
inferredcites →https://doi.org/10.1165/rcmb.2004-0197ocopenalex-snapshot
Mycoplasma pneumoniae Induces Host-Dependent Pulmonary Inflammation and Airway Obstruction in Mice
inferredcites →https://doi.org/10.1165/rcmb.2011-0135ocopenalex-snapshot
Mycoplasma pneumoniae CARDS Toxin Induces Pulmonary Eosinophilic and Lymphocytic Inflammation
inferredcites →https://doi.org/10.1172/jci119045openalex-snapshot
Eosinophil recruitment to the lung in a murine model of allergic inflammation. The role of T cells, chemokines, and adhesion receptors.
inferredcites →https://doi.org/10.1183/09031936.00103307openalex-snapshot
Mycoplasma pneumoniaeinduces airway epithelial cell expression of MUC5AC in asthma
inferredcites →https://doi.org/10.1183/09031936.04.00135703openalex-snapshot
Atypical pathogens and respiratory tract infections
inferredcites →https://doi.org/10.1186/1465-9921-9-48openalex-snapshot
Severe asthma exacerbation: role of acute Chlamydophila pneumoniae and Mycoplasma pneumoniae infection
inferredcites →https://doi.org/10.1203/00006450-198706000-00018openalex-snapshot
Ventilatory Management of Infant Baboons with Hyaline Membrane Disease: The Use of High Frequency Ventilation1
inferredcites →https://doi.org/10.1371/journal.pone.0007562openalex-snapshot
Analysis of Pulmonary Inflammation and Function in the Mouse and Baboon after Exposure to Mycoplasma pneumoniae CARDS Toxin
inferredcites →https://doi.org/10.1371/journal.pone.0022877openalex-snapshot
Cellular Vacuoles Induced by Mycoplasma pneumoniae CARDS Toxin Originate from Rab9-Associated Compartments
inferredcites →https://doi.org/10.1378/chest.06-2415openalex-snapshot
Asthma and Atypical Bacterial Infection
inferredcites →https://doi.org/10.1378/chest.11-0221openalex-snapshot
Persistence of Community-Acquired Respiratory Distress Syndrome Toxin-Producing Mycoplasma pneumoniae in Refractory Asthma
inferredcites →https://doi.org/10.1378/chest.121.6.1782openalex-snapshot
Mycoplasma pneumoniae and Chlamydia pneumoniae in Asthma
inferredcites →https://doi.org/10.3414/me12-01-0005openalex-snapshot
Measuring Inter-observer Agreement in Contour Delineation of Medical Imaging in a Dummy Run Using Fleiss’ Kappa
inferredcites →https://doi.org/10.4049/jimmunol.166.9.5792openalex-snapshot
A Murine IL-4 Receptor Antagonist That Inhibits IL-4- and IL-13-Induced Responses Prevents Antigen-Induced Airway Eosinophilia and Airway Hyperresponsiveness
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4767644openalex-extracted
The RNA-Binding Protein FMRP Induced by Mycoplasma Pneumoniae CARDS Toxin Regulates Multiciliogenesis and Inflammation
inferred← citeshttps://doi.org/10.1007/s00431-026-07514-0openalex-snapshot
Innate and adaptive immunity pathways linking Mycoplasma pneumoniae to pediatric asthma phenotypes
inferred← citeshttps://doi.org/10.1016/j.ddmod.2019.04.001openalex-snapshot
Extracellular matrix components remodeling and lung function parameters in experimental emphysema and allergic asthma: Differences among the mouse strains
inferred← citeshttps://doi.org/10.1016/j.hmedic.2026.100484openalex-snapshot
Mycoplasma pneumoniae-associated diffuse alveolar hemorrhage – A case report and review of its diagnostic intricacies and therapeutic challenges
inferred← citeshttps://doi.org/10.1016/j.iac.2016.03.010openalex-snapshot
Chronic Infection and Severe Asthma
inferred← citeshttps://doi.org/10.1016/j.iac.2019.03.006openalex-snapshot
Bacteria in Asthma Pathogenesis
inferred← citeshttps://doi.org/10.1016/j.jaci.2015.09.032openalex-snapshot
Incident asthma and Mycoplasma pneumoniae: A nationwide cohort study
inferred← citeshttps://doi.org/10.1016/j.jaci.2018.07.021openalex-snapshot
Allergic airway sensitization impairs antibacterial IgG antibody responses during bacterial respiratory tract infections
inferred← citeshttps://doi.org/10.1016/j.jmii.2020.03.030openalex-snapshot
Altered chemokine profile in Refractory Mycoplasma pneumoniae pneumonia infected children
inferred← citeshttps://doi.org/10.1016/j.micpath.2019.02.019openalex-snapshot
House dust mite exposure attenuates influenza A infection in a mouse model of pulmonary allergic inflammation
inferred← citeshttps://doi.org/10.1016/j.micpath.2024.106865openalex-snapshot
Exploring the pathogenicity of Mycoplasma pneumoniae: Focus on community-acquired respiratory distress syndrome toxins
inferred← citeshttps://doi.org/10.1016/j.micpath.2026.108512openalex-snapshot
Development of a high-brightness, genetically stable fluorescent reporter system for Mycoplasma pneumoniae and its application in host-pathogen interaction studies
inferred← citeshttps://doi.org/10.1042/bsr20182201openalex-snapshot
The Mycoplasma pneumoniae HapE alters the cytokine profile and growth of human bronchial epithelial cells
inferred← citeshttps://doi.org/10.1053/j.gastro.2021.10.002openalex-snapshot
Host–Microbiota Interactions in the Esophagus During Homeostasis and Allergic Inflammation
inferred← citeshttps://doi.org/10.1055/s-0044-1779519openalex-snapshot
Periostin Modulating Mycoplasma pneumoniae Pneumonia in Children Related to Th17 Cell Function
inferred← citeshttps://doi.org/10.1080/21505594.2021.1889813openalex-snapshot
Infection strategies of mycoplasmas: Unraveling the panoply of virulence factors
inferred← citeshttps://doi.org/10.1097/aci.0000000000000233openalex-snapshot
Allergen-encoded signals that control allergic responses
inferred← citeshttps://doi.org/10.1111/mmi.70044openalex-snapshot
Bacterial Toxin Exploits Host Membrane Phospholipid as a Receptor for Binding, Entry, and Cytopathogenicity
inferred← citeshttps://doi.org/10.1128/cmr.00114-16openalex-snapshot
Mycoplasma pneumoniae from the Respiratory Tract and Beyond
inferred← citeshttps://doi.org/10.1152/physrev.00040.2016openalex-snapshot
Bacterial-Host Interactions: Physiology and Pathophysiology of Respiratory Infection
inferred← citeshttps://doi.org/10.1165/rcmb.2017-0006ocopenalex-snapshot
The Immunopathologic Effects of Mycoplasma pneumoniae and Community-acquired Respiratory Distress Syndrome Toxin. A Primate Model
inferred← citeshttps://doi.org/10.1186/s12864-015-1801-0openalex-snapshot
Comparative genome analysis of Mycoplasma pneumoniae
inferred← citeshttps://doi.org/10.1186/s12872-021-01940-8openalex-snapshot
Effect of congenital heart disease on the recurrence of cough variant asthma in children
inferred← citeshttps://doi.org/10.1186/s12887-021-02523-4openalex-snapshot
Comparison of different detection methods for Mycoplasma pneumoniae infection in children with community-acquired pneumonia
inferred← citeshttps://doi.org/10.12677/acm.2024.143685openalex-snapshot
Research Progress on Biomarkers of Refractory Mycoplasma pneumoniae Pneumonia in Children
inferred← citeshttps://doi.org/10.12677/acm.2026.1641368openalex-snapshot
Research Progress on Epidemiology and Pathogenesis of Pediatric Mycoplasma pneumoniae Pneumonia
inferred← citeshttps://doi.org/10.1371/journal.pone.0172447openalex-snapshot
Mycoplasma pneumoniae CARDS toxin elicits a functional IgE response in Balb/c mice
inferred← citeshttps://doi.org/10.14740/jocmr3421wopenalex-snapshot
Mycoplasma pneumoniae: A Potentially Severe Infection
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Viral pneumonia in preschool children: current aspects of clinical and paraclinical diagnosis and treatment
inferred← citeshttps://doi.org/10.3345/cep.2019.00360openalex-snapshot
Current perspectives on atypical pneumonia in children
inferred← citeshttps://doi.org/10.3389/falgy.2022.852067openalex-snapshot
Impact of Therapeutics on Unified Immunity During Allergic Asthma and Respiratory Infections
inferred← citeshttps://doi.org/10.3389/falgy.2024.1423938openalex-snapshot
Adjuvant-independent airway sensitization and infection mouse models leading to allergic asthma
inferred← citeshttps://doi.org/10.3389/fimmu.2021.738431openalex-snapshot
Mycoplasma genitalium and M. pneumoniae Regulate a Distinct Set of Protein-Coding Genes in Epithelial Cells
inferred← citeshttps://doi.org/10.3389/fimmu.2026.1724496openalex-snapshot
Immune dysregulation in Mycoplasma pneumoniae pneumonia: mechanistic controversies and clinical translation from inflammatory dysregulation and immune evasion to chronic injury
inferred← citeshttps://doi.org/10.3389/fmicb.2021.766591openalex-snapshot
Community-Acquired Respiratory Distress Syndrome Toxin: Unique Exotoxin for M. pneumoniae
inferred← citeshttps://doi.org/10.3389/fmicb.2025.1589971openalex-snapshot
Whole-genome probe capture sequencing reveals genomic diversity and characteristics of Mycoplasma pneumoniae in Nanjing, China
inferred← citeshttps://doi.org/10.3390/pathogens15050533openalex-snapshot
Pathogenesis and Risk Factors of Post-Infectious Bronchiolitis Obliterans in Children: A Focus on Adenovirus and Mycoplasma Infections
inferred← citeshttps://doi.org/10.36488/cmac.2023.4.332-349openalex-snapshot
Mycoplasma pneumoniae – modern data on the structure, molecular biology and epidemiology of the pathogen
inferred← citeshttps://doi.org/10.3892/mmr.2016.5765openalex-snapshot
Insights into the pathogenesis of Mycoplasma pneumoniae
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Pathogenesis of Mycoplasma pneumoniae: An update
inferred← citeshttps://doi.org/10.5546/aap.2018.179openalex-snapshot
Prevalencia de la infección por Mycoplasma pneumoniae en pacientes pediátricos con exacerbación aguda del asma
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Prevalence of Mycoplasma pneumoniae infection in pediatric patients with acute asthma exacerbation
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Mycoplasma pneumoniae and Recurrent Respiratory Tract Infection Within One Year After Treatment in Infants: Risk Factors and Prevalence
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Additional file 1 of Comparison of different detection methods for Mycoplasma pneumoniae infection in children with community-acquired pneumonia
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