Pregled bibliografske jedinice broj: 300013
CD38 antigen on bronchoalveolar T lymphocytes correlate with alveolitis activity in interstitial lung diseases (ILD)
CD38 antigen on bronchoalveolar T lymphocytes correlate with alveolitis activity in interstitial lung diseases (ILD) // Periodicum Biologorum 97 ((S1) / Branko Vitale (ur.).
Zagreb: Hrvatsko prirodoslovno društvo, 1995. (poster, nije recenziran, sažetak, znanstveni)
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Naslov
CD38 antigen on bronchoalveolar T lymphocytes correlate with alveolitis activity in interstitial lung diseases (ILD)
Autori
Svoboda Beusan, Ivna ; Agbaba Primorac, Rada ; Gomerčić, Dubravka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Periodicum Biologorum 97 ((S1)
/ Branko Vitale - Zagreb : Hrvatsko prirodoslovno društvo, 1995
ISBN
0031-5362
Skup
1995 Annual Meeting of the Croatian Immunological Society
Mjesto i datum
Zagreb, Hrvatska, 23.11.1995. - 24.11.1995
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
CD38; BAL; ILD; Flow cytometry
Sažetak
Recent data suggest that CD38 may be involved in lymphocyte activation and proliferation. The aim of this study was to clarify the role of CD38 in alveolitis pathogenesis. CD38 expression on T cells in bronchoalveolar lavate (BAL) of patients with ILD was assessed by double-staining with CD4/CD38 and CD8/CD38 mAbbs and the data were compared with the same parameters mesured in relevant diseases free subjects (C=8). The ILD samples were obtained from: active sarcoidosis (SA=16), inactive sarcoidosis (SI=15) and idiopathic pulmonary fibrosis (IPF=8). There was variable, but often low number of CD38 cells in control BAL samples. Proportions of CD4, CD38 and CD4CD38 were highly elevated only in SA as compared to SI and IPF, whereas CD8CD38 were generally low. T subset analysis revealed that CD38 was in C predominantly expressed on CD8, whereas in ILD equally on CD4 and CD8 lymphocytes. In three years follow up study eight patients showed CD4CD38 variations depending on the disease activity. As local CD4CD38 expansion correlates with the onset and disease progression, we assume that in SA an intensive recruitment of activated cells is taking place through autocrine fashion by CD38 pathway. Our results indicate that CD38 surface antigen may play a relevant role in SA pathogenesis and could serve as an indicator of alveolitis activity.
Izvorni jezik
Engleski
Znanstvena područja
Biologija
POVEZANOST RADA