Determination of gamma/delta and other T-lymphocyte subsets in bronchoalveolar lavage fluid and peripheral blood from patients with sarcoidosis and idiopathic fibrosis of the lung

被引:25
作者
Gruber, R
Pforte, A
Beer, B
Riethmuller, G
机构
[1] UNIV MUNICH,KLINIKUM INNENSTADT,MED KLIN,W-8000 MUNICH,GERMANY
[2] KLIN LUNGENKRANKHEITEN,GAUTING,GERMANY
关键词
NK cells; CD16; CD56; CD3; CD4; CD8; Langerhans' cell histiocytosis; hypereosinophilic syndrome; flow cytometry;
D O I
10.1111/j.1699-0463.1996.tb00708.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We measured five different lymphocyte subpopulations, including gamma/delta-T cells, in peripheral blood and bronchoalveolar lavage (BAL) fluid from 48 consecutive patients undergoing diagnostic BAL (patients with sarcoidosis (n=19), patients with idiopathic pulmonary fibrosis (IPF; n=11) and patients with other diseases of the lung). Quantitative analysis of CD3+, CD4+, CD8+, CD16/56+ cells and gamma/delta-T cells was done by flow cytometry. The proportion of CD3+ and CD4+ cells in the peripheral blood of patients with sarcoidosis and IPF was significantly diminished, while CD8+ lymphocytes and NK cells were significantly elevated compared to healthy controls. There was no significant difference for the gamma/delta-T cell subpopulation between patients with sarcoidosis, IPF and the control group. The proportion of CD3+ and CD4+ cells in BAL fluid was significantly elevated in sarcoidosis compared to IPF, while CD8+ cells were significantly diminished. Natural kilter cells, defined as CD16/56+ CD3- cells, showed comparable low numbers in sarcoidosis and IPE For gamma/delta-T cells no significant difference was found between patients with sarcoidosis and IPF.
引用
收藏
页码:199 / 205
页数:7
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