Sahin S, Akoğlu T, Direskeneli H, Sen L S, Lawrence R
Department of Haematology and Immunology, Marmara University Medical School, Istanbul, Turkey.
Ann Rheum Dis. 1996 Feb;55(2):128-33. doi: 10.1136/ard.55.2.128.
To study the in vitro adhesion of polymorphonuclear leucocytes (PMNLs) to endothelial cells in patients with Behçet's disease (BD), and the humoral and cellular factors which may contribute to adhesion.
A total of 118 patients with BD and 60 healthy controls were studied. In vitro adhesion of chromium-51 labelled normal neutrophils to human umbilical vascular endothelial cell (HUVEC) monolayers were studied in the presence of normal serum or serum obtained from patients with BD. Adhesion of neutrophils from patients with BD to HUVEC stimulated with tumour necrosis factor (TNF), interleukin-1 (IL-1), and lipopolysaccharide (LPS) and adhesion molecule (CD11a, CD11b, CD18 and L-selectin) expression on the patient's neutrophils and lymphocytes were determined, and the serum concentration of IL-8 was measured.
Sera from patients with BD were found to enhance the adherence of normal PMNLs to HUVEC monolayers in vitro. Patients' sera induced an increase in surface expression of CD11a and CD18 on normal neutrophils and intercellular adhesion molecule-1 (ICAM-1) expression on HUVECs. The number of CD11a positive neutrophils was greater in the blood of patients with BD than in that of healthy controls (89.4% v 71%; p < 0.001). Pretreatment of HUVECs with IL-1 alpha, TNF alpha or LPS resulted in an increased adhesion of patients' PMNLs greater than that observed for normal PMNLs. Monoclonal antibodies to CD11a, CD11b, CD18, and ICAM-1 caused varying degrees of inhibition of neutrophil adhesion. The concentration of IL-8 was also found to be significantly increased in sera of patients with BD (490 (SD 470) pg/ml) compared with normal controls (97.5 (56.3) pg/ml).
Abnormalities of neutrophils, endothelial cells, or both, have been suggested to be responsible for many of the clinical manifestations of BD. Our findings may explain the underlying mechanism of neutrophil accumulation in Behçet's lesions.
研究白塞病(BD)患者多形核白细胞(PMNLs)与内皮细胞的体外黏附情况,以及可能促成黏附的体液和细胞因子。
共研究了118例BD患者和60例健康对照者。在正常血清或BD患者血清存在的情况下,研究铬-51标记的正常中性粒细胞与人脐静脉血管内皮细胞(HUVEC)单层的体外黏附。测定BD患者中性粒细胞与经肿瘤坏死因子(TNF)、白细胞介素-1(IL-1)和脂多糖(LPS)刺激的HUVEC的黏附情况,以及患者中性粒细胞和淋巴细胞上黏附分子(CD11a、CD11b、CD18和L-选择素)的表达,并检测血清IL-8浓度。
发现BD患者血清可增强正常PMNLs体外对HUVEC单层的黏附。患者血清可诱导正常中性粒细胞上CD11a和CD18的表面表达增加,以及HUVEC上细胞间黏附分子-1(ICAM-1)的表达增加。BD患者血液中CD11a阳性中性粒细胞的数量高于健康对照者(89.4%对71%;p<0.001)。用IL-1α、TNFα或LPS预处理HUVEC后,患者PMNLs的黏附增加程度大于正常PMNLs。针对CD11a、CD11b、CD18和ICAM-1的单克隆抗体可引起中性粒细胞黏附的不同程度抑制。还发现BD患者血清中IL-8浓度与正常对照者相比显著升高(490(标准差470)pg/ml对97.5(56.3)pg/ml)。
中性粒细胞、内皮细胞或两者的异常被认为是BD许多临床表现的原因。我们的研究结果可能解释了白塞病病变中中性粒细胞积聚的潜在机制。