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High Peripheral Blood Th17 Percent Associated with Poor Lung Function in Cystic Fibrosis
by
Roddam, Louise F.
, Beggs, Sean A.
, Cooley, Margaret A.
, Reid, David W.
, Hudson, Jo B.
, Mulcahy, Emily M.
in
Adolescent
/ Adolescents
/ Adult
/ Adults
/ Allergies
/ Analysis
/ Blood
/ Blood tests
/ CD4 antigen
/ Child
/ Child, Preschool
/ Children
/ Chronic infection
/ Cystic fibrosis
/ Cystic Fibrosis - complications
/ Cystic Fibrosis - immunology
/ Cytokines
/ Disease
/ Female
/ Foxp3 protein
/ Genotypes
/ Helper cells
/ Hospitals
/ Humans
/ Infant
/ Infections
/ Interferon
/ Interleukin 10
/ Interleukin 17
/ Interleukin 4
/ Leukocytes, Mononuclear
/ Lung - immunology
/ Lung - microbiology
/ Lungs
/ Lymphocytes
/ Lymphocytes T
/ Male
/ Medicine
/ Middle Aged
/ Peripheral blood mononuclear cells
/ Pseudomonas aeruginosa
/ Pseudomonas aeruginosa - isolation & purification
/ Pseudomonas Infections - complications
/ Pseudomonas Infections - diagnosis
/ Pseudomonas Infections - immunology
/ Respiratory function
/ Respiratory Tract Infections - complications
/ Respiratory Tract Infections - diagnosis
/ Respiratory Tract Infections - immunology
/ Software
/ Statistical analysis
/ Statistics
/ T cells
/ Th17 Cells - immunology
/ Transforming growth factors
/ Young Adult
/ γ-Interferon
2015
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High Peripheral Blood Th17 Percent Associated with Poor Lung Function in Cystic Fibrosis
by
Roddam, Louise F.
, Beggs, Sean A.
, Cooley, Margaret A.
, Reid, David W.
, Hudson, Jo B.
, Mulcahy, Emily M.
in
Adolescent
/ Adolescents
/ Adult
/ Adults
/ Allergies
/ Analysis
/ Blood
/ Blood tests
/ CD4 antigen
/ Child
/ Child, Preschool
/ Children
/ Chronic infection
/ Cystic fibrosis
/ Cystic Fibrosis - complications
/ Cystic Fibrosis - immunology
/ Cytokines
/ Disease
/ Female
/ Foxp3 protein
/ Genotypes
/ Helper cells
/ Hospitals
/ Humans
/ Infant
/ Infections
/ Interferon
/ Interleukin 10
/ Interleukin 17
/ Interleukin 4
/ Leukocytes, Mononuclear
/ Lung - immunology
/ Lung - microbiology
/ Lungs
/ Lymphocytes
/ Lymphocytes T
/ Male
/ Medicine
/ Middle Aged
/ Peripheral blood mononuclear cells
/ Pseudomonas aeruginosa
/ Pseudomonas aeruginosa - isolation & purification
/ Pseudomonas Infections - complications
/ Pseudomonas Infections - diagnosis
/ Pseudomonas Infections - immunology
/ Respiratory function
/ Respiratory Tract Infections - complications
/ Respiratory Tract Infections - diagnosis
/ Respiratory Tract Infections - immunology
/ Software
/ Statistical analysis
/ Statistics
/ T cells
/ Th17 Cells - immunology
/ Transforming growth factors
/ Young Adult
/ γ-Interferon
2015
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High Peripheral Blood Th17 Percent Associated with Poor Lung Function in Cystic Fibrosis
by
Roddam, Louise F.
, Beggs, Sean A.
, Cooley, Margaret A.
, Reid, David W.
, Hudson, Jo B.
, Mulcahy, Emily M.
in
Adolescent
/ Adolescents
/ Adult
/ Adults
/ Allergies
/ Analysis
/ Blood
/ Blood tests
/ CD4 antigen
/ Child
/ Child, Preschool
/ Children
/ Chronic infection
/ Cystic fibrosis
/ Cystic Fibrosis - complications
/ Cystic Fibrosis - immunology
/ Cytokines
/ Disease
/ Female
/ Foxp3 protein
/ Genotypes
/ Helper cells
/ Hospitals
/ Humans
/ Infant
/ Infections
/ Interferon
/ Interleukin 10
/ Interleukin 17
/ Interleukin 4
/ Leukocytes, Mononuclear
/ Lung - immunology
/ Lung - microbiology
/ Lungs
/ Lymphocytes
/ Lymphocytes T
/ Male
/ Medicine
/ Middle Aged
/ Peripheral blood mononuclear cells
/ Pseudomonas aeruginosa
/ Pseudomonas aeruginosa - isolation & purification
/ Pseudomonas Infections - complications
/ Pseudomonas Infections - diagnosis
/ Pseudomonas Infections - immunology
/ Respiratory function
/ Respiratory Tract Infections - complications
/ Respiratory Tract Infections - diagnosis
/ Respiratory Tract Infections - immunology
/ Software
/ Statistical analysis
/ Statistics
/ T cells
/ Th17 Cells - immunology
/ Transforming growth factors
/ Young Adult
/ γ-Interferon
2015
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High Peripheral Blood Th17 Percent Associated with Poor Lung Function in Cystic Fibrosis
Journal Article
High Peripheral Blood Th17 Percent Associated with Poor Lung Function in Cystic Fibrosis
2015
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Overview
People with cystic fibrosis (CF) have been reported to make lung T cell responses that are biased towards T helper (Th) 2 or Th17. We hypothesized that CF-related T cell regulatory defects could be detected by analyzing CD4+ lymphocyte subsets in peripheral blood. Peripheral blood mononuclear cells from 42 CF patients (6 months-53 years old) and 78 healthy controls (2-61 years old) were analyzed for Th1 (IFN-γ+), Th2 (IL-4+), Th17 (IL-17+), Treg (FOXP3+), IL-10+ and TGF-β+ CD4+ cells. We observed higher proportions of Treg, IL-10+ and TGF-β+ CD4+ cells in CF adults (≥ 18 years old), but not children/adolescents, compared with controls. Within the CF group, high TGF-β+% was associated with chronic Pseudomonas aeruginosa lung infection (p < 0.006). We observed no significant differences between control and CF groups in the proportions of Th1, Th2 or Th17 cells, and no association within the CF group of any subset with sex, CFTR genotype, or clinical exacerbation. However, high Th17% was strongly associated with poor lung function (FEV1 % predicted) (p = 0.0008), and this association was strongest when both lung function testing and blood sampling were performed within one week. Our results are consistent with reports of CF as a Th17 disease and suggest that peripheral blood Th17 levels may be a surrogate marker of lung function in CF.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Adult
/ Adults
/ Analysis
/ Blood
/ Child
/ Children
/ Cystic Fibrosis - complications
/ Cystic Fibrosis - immunology
/ Disease
/ Female
/ Humans
/ Infant
/ Lungs
/ Male
/ Medicine
/ Peripheral blood mononuclear cells
/ Pseudomonas aeruginosa - isolation & purification
/ Pseudomonas Infections - complications
/ Pseudomonas Infections - diagnosis
/ Pseudomonas Infections - immunology
/ Respiratory Tract Infections - complications
/ Respiratory Tract Infections - diagnosis
/ Respiratory Tract Infections - immunology
/ Software
/ T cells
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