Ziora D, Dworniczak S, Niepsuj G, Grzanka P, Cieślicki J, Kozielski J, Ciekalska K, Jarosz W, Sielska-Pytek E
Kliniki Ftizjopneumonologii S.A.M. w Zabrzu.
Pneumonol Alergol Pol. 2000;68(7-8):336-46.
The aim of the study was to evaluate the concentrations of TNF-alpha and GM-CSF in double BAL (2 x 120 ml) from two different lung segments: (s.A) from upper lobe with the most and (s.B) from lower lobe with the least extensive involvement estimated by high resolution computed tomography (HRCT). Examined group consisted of 28 non-smoking sarcoid patients with homogenous, regular distribution of nodular opacities in conventional chest X-ray (14 F, 14M aged 19-54). In examined patients 16 had nonhomogenous distribution (ND) and 12 had regular distribution (RD) of HRCT changes. Eleven healthy volunteers served as controls. In patients with sarcoidosis we observed the significantly higher concentrations (p < 0.01) of TNF-alpha (3.18 pg/ml, 2.64 pg/ml) and GM-CSF (1.01 pg/ml, 0.95 pg/ml) respectively in BAL fluid from s.A and s.B in comparison with BAL from s.Abis and s.Bbis in control group (TNF-alpha: 0.46 pg/ml, 0.47 pg/ml and GM-CSF: 0.28 pg/ml, 0.31 pg/ml respectively). Mean concentration of TNF-alpha in BAL from s.A (3.77 pg/ml) in ND group was significantly higher than in BAL from s.B in RD group (2.91 pg/ml). TNF-alpha in BAL from s.A in active sarcoidosis was higher than in BAL from s.A and s.B in non-active sarcoidosis. Concentrations of TNF-alpha in BAL from both s.A and s.B correlated positively with CD4/CD8 ratio, percentage of lymphocytes, lymphocytes HLA-DR+ and absolute number of CD4 cells and negatively with CD8 cells estimated in BAL from these lung segments. In patients with indications to therapy the level of GM-CSF in BAL from s.A (1.44 pg/ml) was significantly higher (p < 0.05) than in BAL from s.A (0.64 pg/ml) in patients without indications to treatment. We conclude that TNF-alpha and GM-CSF may be involved in sarcoidosis pathogenesis and TNF-alpha may be useful in estimation of sarcoidosis activity.
本研究的目的是评估来自两个不同肺段的双份支气管肺泡灌洗(2×120 ml)中TNF-α和GM-CSF的浓度:(s.A)来自上叶,受累范围最广;(s.B)来自下叶,受累范围最小,通过高分辨率计算机断层扫描(HRCT)评估。研究组由28例非吸烟结节病患者组成,其在传统胸部X线检查中结节状阴影分布均匀、规则(14例女性,14例男性,年龄19 - 54岁)。在研究的患者中,16例HRCT改变分布不均(ND),12例分布规则(RD)。11名健康志愿者作为对照。与对照组s.Abis和s.Bbis的支气管肺泡灌洗相比,结节病患者中,s.A和s.B的支气管肺泡灌洗液中TNF-α(分别为3.18 pg/ml、2.64 pg/ml)和GM-CSF(分别为1.01 pg/ml、0.95 pg/ml)的浓度显著更高(p < 0.01)(TNF-α:分别为0.46 pg/ml、0.47 pg/ml;GM-CSF:分别为0.28 pg/ml、0.31 pg/ml)。ND组s.A的支气管肺泡灌洗中TNF-α的平均浓度(3.77 pg/ml)显著高于RD组s.B的支气管肺泡灌洗(2.91 pg/ml)。活动期结节病患者s.A的支气管肺泡灌洗中TNF-α高于非活动期结节病患者s.A和s.B的支气管肺泡灌洗。s.A和s.B的支气管肺泡灌洗中TNF-α的浓度与CD4/CD8比值、淋巴细胞百分比、淋巴细胞HLA-DR +以及这些肺段支气管肺泡灌洗中CD4细胞的绝对数量呈正相关,与CD8细胞呈负相关。有治疗指征的患者中,s.A的支气管肺泡灌洗中GM-CSF水平(1.44 pg/ml)显著高于无治疗指征患者s.A的支气管肺泡灌洗(0.64 pg/ml)(p < 0.05)。我们得出结论,TNF-α和GM-CSF可能参与结节病的发病机制,TNF-α可能有助于评估结节病的活动度。