Komiyama A, Ichikawa M, Kanda H, Aoyama K, Yasui K, Yamazaki M, Kawai H, Miyagawa Y, Akabane T
Department of Pediatrics, Shinshu University School of Medicine, Matsumoto, Japan.
Clin Exp Immunol. 1988 Sep;73(3):500-4.
Monocytes in a familial monocyte disorder, a recently recognized primary immunodeficiency syndrome, with impaired phagocytic functions were studied for their ability to produce interleukin 1 (IL-1) as well as the surface property. Monocytes from two children (siblings) with the disorder possessed CD11b, CD13, CD14, CD33, Ia and LFA-1/Mac-1/p150,95 beta subunit antigens as determined by flow cytometry. Electron microscopic cytochemistry showed that the monocytes had surface glycoproteins reactive with four representative lectins. The IL-1 production by monocytes was assayed in the two patients and compared with that in six children with primary immunodeficiency syndromes and some monocyte abnormalities; three had congenital neutropenia, two had hyper-IgE syndrome, and one had defective monocyte chemotaxis. Monocyte culture supernatants were prepared with stimulation by lipopolysaccharide or silica, and their IL-1 activity was measured by the mouse thymocyte-proliferation assay. The patients' monocytes were defective in IL-1 production: the values were less than 1.0% of the control monocyte values (n = 12) and were in contrast with those of congenital neutropenia monocytes of 186.2% to 204.3%. These results demonstrate a familial monocyte disorder which is characteristic among the immunodeficiency syndromes with regard to the defective IL-1 production and the impaired phagocytic functions.
在一种家族性单核细胞疾病(一种最近才被认识的原发性免疫缺陷综合征,其吞噬功能受损)中,研究了单核细胞产生白细胞介素1(IL-1)的能力以及其表面特性。通过流式细胞术测定,来自两名患有该疾病的儿童(兄弟姐妹)的单核细胞具有CD11b、CD13、CD14、CD33、Ia和LFA-1/Mac-1/p150,95β亚基抗原。电子显微镜细胞化学显示,这些单核细胞具有与四种代表性凝集素反应的表面糖蛋白。对两名患者的单核细胞产生IL-1的情况进行了测定,并与六名患有原发性免疫缺陷综合征且有一些单核细胞异常的儿童进行了比较;其中三名患有先天性中性粒细胞减少症,两名患有高IgE综合征,一名单核细胞趋化性有缺陷。用脂多糖或二氧化硅刺激制备单核细胞培养上清液,并通过小鼠胸腺细胞增殖试验测量其IL-1活性。患者的单核细胞在产生IL-1方面存在缺陷:其值低于对照单核细胞值的1.0%(n = 12),这与先天性中性粒细胞减少症单核细胞的值(186.2%至204.3%)形成对比。这些结果证明了一种家族性单核细胞疾病,在免疫缺陷综合征中,它在IL-1产生缺陷和吞噬功能受损方面具有特征性。