IL-4 polymorphisms, HRCT score and lung tissue markers in idiopathic pulmonary fibrosis
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
23911740
DOI
10.1016/j.humimm.2013.07.011
PII: S0198-8859(13)00212-7
Knihovny.cz E-zdroje
- MeSH
- alely MeSH
- biologické markery MeSH
- biopsie MeSH
- dospělí MeSH
- eozinofily metabolismus MeSH
- fenotyp MeSH
- genotyp MeSH
- idiopatická plicní fibróza diagnóza genetika MeSH
- interleukin-4 genetika MeSH
- lidé středního věku MeSH
- lidé MeSH
- makrofágy metabolismus MeSH
- plíce imunologie metabolismus patologie MeSH
- počet leukocytů MeSH
- polymorfismus genetický * MeSH
- receptor interleukinu-4 - alfa-podjednotka genetika metabolismus MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- biologické markery MeSH
- interleukin-4 MeSH
- receptor interleukinu-4 - alfa-podjednotka MeSH
AIMS: We studied the influence of IL-4 gene polymorphisms on the IPF phenotype, i.e., extent of radiological changes (HRCT interstitial (IS) and alveolar (AS) score) and histopathological markers from lung biopsies. PATIENTS AND METHODS: 46 IPF patients underwent genotyping, 43 of them had HRCT and 14 patients had a surgical lung biopsy. The HRCT scans were evaluated for AS and IS. The histopathological evaluation comprised myofibroblast foci (MF), intensity of inflammation and fibrosis (Ashcroft score) and numbers of eosinophils and granulomas. For immunohistochemical evaluation primary antibodies against PAR-2, CD124, TGF beta, YY-1 and TSLP were used. The IL-4 and IL-4 R alpha gene polymorphisms were characterized. RESULTS: We found a correlation between eosinophils in lung biopsies and AS. The Ashcroft score was higher in IL-4 HA 2 GCC and MF were more frequent in IL-4 HA 2 TCC carriers. A relationship was found between IL-4 (-1098) A2 T and PAR-2 expression and IL-4 (-590) A1 T, IL-4 HA1TTT and CD124 expression. AS was lower in IL-4 (-590) A1 C, in IL-4 HA1 TCC and in IL-4RA (+1902) A1 A carriers. CONCLUSIONS: We suggest that the polymorphisms of IL-4 genes might influence the phenotype of IPF reflected by histopathological changes in lung biopsies and HRCT score.
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