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dc.creatorPapiris, S. A.en
dc.creatorKollintza, A.en
dc.creatorKaratza, M.en
dc.creatorManali, E. D.en
dc.creatorSotiropoulou, C.en
dc.creatorMilic-Emili, J.en
dc.creatorRoussos, C.en
dc.creatorDaniil, Z.en
dc.date.accessioned2015-11-23T10:44:44Z
dc.date.available2015-11-23T10:44:44Z
dc.date.issued2007
dc.identifier10.1186/1476-9255-4-14
dc.identifier.issn14769255
dc.identifier.urihttp://hdl.handle.net/11615/31995
dc.description.abstractBackground. Recently it was shown that in Idiopathic Pulmonary Fibrosis (IPF) tissue infiltrating CD8+ T lymphocytes (TLs) are associated with breathlessness and physiological indices of disease severity, as well as that CD8+ TLs recovered by bronchoalveolar lavage (BAL) relate to those infiltrating lung tissue. Since BAL is a far less invasive technique than tissue biopsy to study mechanisms in IPF we further investigated the usefulness offered by this means by studying the relationship between BAL macrophages, neutrophils, eosinophils, CD3+, CD4+, CD8+, CD8+/38+ TLs and CD4+/CD8+ ratio with breathlessness and physiological indices. Patients and methods. 27 IPF patients, 63 ± 9 years of age were examined. Cell counts were expressed as percentages of total cells and TLs were evaluated by flow cytometry. FEV 1, FVC, TLC, RV, DLCO, PaO2, and PaCO2 were measured in all. Breathlessness was assessed by the Medical Research Council (MRC) chronic dyspnoea scale. Results. CD8+ TLs correlated positively (rs = 0.46, p = 0.02), while CD4+/CD8+ ratio negatively (rs = -0.54, p = 0.006) with the MRC grade. CD 8+ TLs correlated negatively with RV (rs = -0.50, p = 0.017). CD8+/38+ TLs were negatively related to the FEV1 and FVC (rs = -0.53, p = 0.03 and rs = -0.59, p = 0.02, respectively). Neutrophils correlated positively with the MRC grade (r s = 0.42, p = 0.03), and negatively with the DLCO (rs = -0.54, p = 0.005), PaO2 (rs = -0.44, p = 0.03), and PaCO2 (rs = -0.52, p = 0.01). Conclusion. BAL CD 8+ TLs associations with physiological and clinical indices seem to indicate their implication in IPF pathogenesis, confirming our previous tissue study. © 2007 Papiris et al; licensee BioMed Central Ltd.en
dc.source.urihttp://www.scopus.com/inward/record.url?eid=2-s2.0-34447103402&partnerID=40&md5=a39a36b5b0721e85da7189bd2dbea29e
dc.subjectCD3 antigenen
dc.subjectCD4 antigenen
dc.subjectCD8 antigenen
dc.subjectadulten
dc.subjectcarbon dioxide tensionen
dc.subjectCD8+ T lymphocyteen
dc.subjectcell counten
dc.subjectclinical articleen
dc.subjectdyspneaen
dc.subjecteosinophilen
dc.subjectfemaleen
dc.subjectfibrosing alveolitisen
dc.subjectflow cytometryen
dc.subjectforced expiratory volumeen
dc.subjecthumanen
dc.subjectlung diffusionen
dc.subjectlung lavageen
dc.subjectmacrophageen
dc.subjectmaleen
dc.subjectmedical research council chronic dyspnea scaleen
dc.subjectneutrophilen
dc.subjectoxygen tensionen
dc.subjectpathogenesisen
dc.subjectrating scaleen
dc.subjectresidual volumeen
dc.subjectreviewen
dc.subjecttotal lung capacityen
dc.titleCD8+T lymphocytes in bronchoalveolar lavage in idiopathic pulmonary fibrosisen
dc.typejournalArticleen


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