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Autor(en) / Beteiligte
Titel
Patients with cystic fibrosis have inducible IL-17+ IL-22+ memory cells in lung draining lymph nodes
Ist Teil von
  • Journal of allergy and clinical immunology, 2013-04, Vol.131 (4), p.1117-1129.e5
Ort / Verlag
New York, NY: Mosby, Inc
Erscheinungsjahr
2013
Quelle
MEDLINE
Beschreibungen/Notizen
  • Background IL-17 is an important cytokine signature of the TH differentiation pathway TH 17. This T-cell subset is crucial in mediating autoimmune disease or antimicrobial immunity in animal models, but its presence and role in human disease remain to be completely characterized. Objective We set out to determine the frequency of TH 17 cells in patients with cystic fibrosis (CF), a disease in which there is recurrent infection with known pathogens. Methods Explanted lungs from patients undergoing transplantation or organ donors (CF samples = 18; non-CF, nonbronchiectatic samples = 10) were collected. Hilar nodes and parenchymal lung tissue were processed and examined for TH 17 signature by using immunofluorescence and quantitative real-time PCR. T cells were isolated and stimulated with antigens from Pseudomonas aeruginosa and Aspergillus species. Cytokine profiles and staining with flow cytometry were used to assess the reactivity of these cells to antigen stimulation. Results We found a strong IL-17 phenotype in patients with CF compared with that seen in control subjects without CF. Within this tissue, we found pathogenic antigen–responsive CD4+ IL-17+ cells. There were double-positive IL-17+ IL-22+ cells [TH 17(22)], and the IL-22+ population had a higher proportion of memory characteristics. Antigen-specific TH 17 responses were stronger in the draining lymph nodes compared with those seen in matched parenchymal lungs. Conclusion Inducible proliferation of TH 17(22) with memory cell characteristics is seen in the lungs of patients with CF. The function of these individual subpopulations will require further study regarding their development. T cells are likely not the exclusive producers of IL-17 and IL-22, and this will require further characterization.
Sprache
Englisch
Identifikatoren
ISSN: 0091-6749
eISSN: 1097-6825
DOI: 10.1016/j.jaci.2012.05.036
Titel-ID: cdi_proquest_miscellaneous_1322732013
Format
Schlagworte
Adult, Aged, Allergy and Immunology, Antigens, Antigens, Bacterial - immunology, Antigens, Bacterial - pharmacology, Antigens, Fungal - immunology, Antigens, Fungal - pharmacology, Aspergillus - chemistry, Aspergillus species, Biological and medical sciences, Case-Control Studies, Cell Proliferation - drug effects, chronic infectious disease, Chronic obstructive pulmonary disease, Cystic fibrosis, Cystic Fibrosis - genetics, Cystic Fibrosis - immunology, Cystic Fibrosis - pathology, Disease, Errors of metabolism, Female, Fundamental and applied biological sciences. Psychology, Fundamental immunology, Fungal infections, Gene Expression, Human subjects, Humans, IL-17, IL-22, Immune system, Immunologic Memory, Immunopathology, Immunophenotyping, Interleukin-17 - genetics, Interleukin-17 - immunology, Interleukin-22, Interleukins - genetics, Interleukins - immunology, Lung - drug effects, Lung - immunology, Lung - pathology, lung transplant, Lungs, Lymph Nodes - drug effects, Lymph Nodes - immunology, Lymph Nodes - pathology, Lymphocyte Activation - drug effects, Male, Medical sciences, memory T-cell response, Metabolic diseases, Middle Aged, Miscellaneous hereditary metabolic disorders, Pseudomonas aeruginosa - chemistry, Pseudomonas species, Review boards, Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis, Studies, TH17, Th17 Cells - drug effects, Th17 Cells - immunology, Th17 Cells - pathology, TH22, Transplants & implants

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