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A 1-Year Experience with Human Metapneumovirus in Children Aged <5 Years

The Journal of infectious diseases, 2004-04, Vol.189 (8), p.1388-1396

2004

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IL-10 and RANTES are Elevated in Nasopharyngeal Secretions of Children with Respiratory Syncytial Virus Infection

Allergology international, 2007, Vol.56 (2), p.157-163

2007

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IL-10 gene polymorphism at −1082 A/G is associated with severe rhinovirus bronchiolitis in infants

Pediatric pulmonology, 2008-04, Vol.43 (4), p.391-395

2008

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IL-10 Gene Polymorphisms Are Associated with Post-Bronchiolitis Lung Function Abnormalities at Six Years of Age

PloS one, 2015-10, Vol.10 (10), p.e0140799-e0140799

2015

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IL-12-Activated NK Cells Reduce Lung Eosinophilia to the Attachment Protein of Respiratory Syncytial Virus But Do Not Enhance the Severity of Illness in CD8 T Cell-Immunodeficient Conditions

The Journal of immunology (1950), 2000-12, Vol.165 (12), p.7109-7115

2000

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IL-12 treatment attenuates T helper cell type 2 and B cell responses but does not improve vaccine-enhanced lung illness

The Journal of immunology (1950), 1997-07, Vol.159 (1), p.328-334

1997

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IL-12p40 and IL-18 Modulate Inflammatory and Immune Responses to Respiratory Syncytial Virus Infection

The Journal of immunology (1950), 2004-09, Vol.173 (6), p.4040-4049

2004

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IL-12p40 gene-deficient BALB/c mice exhibit lower weight loss, reduced lung pathology and decreased sensitization to allergen in response to infection with pneumonia virus of mice

Virology (New York, N.Y.), 2016-10, Vol.497, p.1-10

2016

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IL-13 genetic polymorphism identifies children with late wheezing after respiratory syncytial virus infection

Journal of allergy and clinical immunology, 2007-05, Vol.119 (5), p.1086-1091

2007

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IL-13-Induced Airway Hyperreactivity During Respiratory Syncytial Virus Infection Is STAT6 Dependent

The Journal of immunology (1950), 2001-03, Vol.166 (5), p.3542-3548

2001

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IL-13 is associated with reduced illness and replication in primary respiratory syncytial virus infection in the mouse

Microbes and infection, 2006-11, Vol.8 (14), p.2880-2889

2006

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IL-13 Is Required for Eosinophil Entry into the Lung during Respiratory Syncytial Virus Vaccine-Enhanced Disease

The Journal of immunology (1950), 2008-02, Vol.180 (4), p.2376-2384

2008

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IL-13 Is Sufficient for Respiratory Syncytial Virus G Glycoprotein-Induced Eosinophilia After Respiratory Syncytial Virus Challenge

The Journal of immunology (1950), 2003-02, Vol.170 (4), p.2037-2045

2003

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IL-13 regulates Th17 secretion of IL-17A in an IL-10-dependent manner

The Journal of immunology (1950), 2012-02, Vol.188 (3), p.1027-1035

2012

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A 14-year Prospective Study of Human Coronavirus Infections in Hospitalized Children: Comparison With Other Respiratory Viruses

The Pediatric infectious disease journal, 2020-08, Vol.39 (8), p.653-657

2020

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IL-15 regulates memory CD8+ T cell O-glycan synthesis and affects trafficking

The Journal of clinical investigation, 2014-03, Vol.124 (3), p.1013-1026

2014

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A 16-amino acid peptide of respiratory syncytial virus 1A protein contains two overlapping T cell-stimulating sites distinguishable by class II MHC restriction elements

The Journal of immunology (1950), 1989-11, Vol.143 (9), p.2790-2796

1989

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IL-17 boosts proinflammatory outcome of antiviral response in human cells

The Journal of immunology (1950), 2011-11, Vol.187 (10), p.5357-5362

2011

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IL-17A induces signal transducers and activators of transcription-6-independent airway mucous cell metaplasia

American journal of respiratory cell and molecular biology, 2013-06, Vol.48 (6), p.711-716

2013

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IL‐17A is a common and critical driver of impaired lung function and immunopathology induced by influenza virus, rhinovirus and respiratory syncytial virus

Respirology (Carlton, Vic.), 2021-11, Vol.26 (11), p.1049-1059

2021

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IL-17A plays a critical role in RSV infection in children and mice

Virology journal, 2023-02, Vol.20 (1), p.30-30, Article 30

2023

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IL‐17E (IL‐25) and IL‐17RB promote respiratory syncytial virus‐induced pulmonary disease

Journal of leukocyte biology, 2014-05, Vol.95 (5), p.809-815

2014

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The 1B (NS2), 1C (NS1) and N Proteins of Human Respiratory Syncytial Virus (RSV) of Antigenic Subgroups A and B: Sequence Conservation and Divergence within RSV Genomic RNA

Journal of general virology, 1989-06, Vol.70 (6), p.1539-1547

1989

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1st WHO International Standard antiserum to RSV: Availability and benefits for RSV vaccine development (Commentary on the collaborative study report published in the vaccine journal (Vaccine 2018 36: 7641–7649))

Vaccine, 2019-07, Vol.37 (31), p.4233-4235

Knezevic, Ivana

2019

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IL-1α is required for T cell-driven weight loss after respiratory viral infection

Mucosal immunology, 2024-04, Vol.17 (2), p.272-287

2024

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A 1-Year Experience with Human Metapneumovirus in Children Aged <5 Years

IL-10 and RANTES are Elevated in Nasopharyngeal Secretions of Children with Respiratory Syncytial Virus Infection

IL-10 gene polymorphism at −1082 A/G is associated with severe rhinovirus bronchiolitis in infants

IL-10 Gene Polymorphisms Are Associated with Post-Bronchiolitis Lung Function Abnormalities at Six Years of Age

IL-12-Activated NK Cells Reduce Lung Eosinophilia to the Attachment Protein of Respiratory Syncytial Virus But Do Not Enhance the Severity of Illness in CD8 T Cell-Immunodeficient Conditions

IL-12 treatment attenuates T helper cell type 2 and B cell responses but does not improve vaccine-enhanced lung illness

IL-12p40 and IL-18 Modulate Inflammatory and Immune Responses to Respiratory Syncytial Virus Infection

IL-12p40 gene-deficient BALB/c mice exhibit lower weight loss, reduced lung pathology and decreased sensitization to allergen in response to infection with pneumonia virus of mice

IL-13 genetic polymorphism identifies children with late wheezing after respiratory syncytial virus infection

IL-13-Induced Airway Hyperreactivity During Respiratory Syncytial Virus Infection Is STAT6 Dependent

IL-13 is associated with reduced illness and replication in primary respiratory syncytial virus infection in the mouse

IL-13 Is Required for Eosinophil Entry into the Lung during Respiratory Syncytial Virus Vaccine-Enhanced Disease

IL-13 Is Sufficient for Respiratory Syncytial Virus G Glycoprotein-Induced Eosinophilia After Respiratory Syncytial Virus Challenge

IL-13 regulates Th17 secretion of IL-17A in an IL-10-dependent manner

A 14-year Prospective Study of Human Coronavirus Infections in Hospitalized Children: Comparison With Other Respiratory Viruses

IL-15 regulates memory CD8+ T cell O-glycan synthesis and affects trafficking

A 16-amino acid peptide of respiratory syncytial virus 1A protein contains two overlapping T cell-stimulating sites distinguishable by class II MHC restriction elements

IL-17 boosts proinflammatory outcome of antiviral response in human cells

IL-17A induces signal transducers and activators of transcription-6-independent airway mucous cell metaplasia

IL‐17A is a common and critical driver of impaired lung function and immunopathology induced by influenza virus, rhinovirus and respiratory syncytial virus

IL-17A plays a critical role in RSV infection in children and mice

IL‐17E (IL‐25) and IL‐17RB promote respiratory syncytial virus‐induced pulmonary disease

The 1B (NS2), 1C (NS1) and N Proteins of Human Respiratory Syncytial Virus (RSV) of Antigenic Subgroups A and B: Sequence Conservation and Divergence within RSV Genomic RNA

1st WHO International Standard antiserum to RSV: Availability and benefits for RSV vaccine development (Commentary on the collaborative study report published in the vaccine journal (Vaccine 2018 36: 7641–7649))

IL-1α is required for T cell-driven weight loss after respiratory viral infection

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