Andreesen R, Brugger W, Kunze R, Stille W, von Briesen H
Medizinische Klinik der Albert-Ludwigs-Universität Freiburg Hugstetter, FRG.
Res Virol. 1990 Mar-Apr;141(2):217-24. doi: 10.1016/0923-2516(90)90024-d.
To look for possible defects in cells of the monocyte/macrophage system, blood monocytes from patients infected with human immunodeficiency virus (HIV) were cultured on hydrophobic Teflon for 7 days and their ability to differentiate into mature macrophages in the presence of serum was followed. The following parameters were studied as indicative of successful terminal maturation: (1) the expression of maturation-associated antigens (transferrin receptor, surface transferrin, the BA-2 antigen, MAX antigens), (2) the disappearance of the MOP15 antigen, and (3) a more than 20-fold increase in intracellular ferritin concentration. It was found that the patients' blood monocytes did not differentiate in vitro but rather remained immature precursor cells. If the same holds true in vivo, the results could indicate that the pathophysiology of the acquired immunodeficiency syndrome (AIDS) may be, to a large extent, linked with the functional consequences of this impaired monocyte-to-macrophage maturation.
为了寻找单核细胞/巨噬细胞系统细胞中可能存在的缺陷,将感染人类免疫缺陷病毒(HIV)患者的血液单核细胞在疏水性聚四氟乙烯上培养7天,并观察其在血清存在下分化为成熟巨噬细胞的能力。研究了以下参数作为成功终末成熟的指标:(1)成熟相关抗原(转铁蛋白受体、表面转铁蛋白、BA-2抗原、MAX抗原)的表达;(2)MOP15抗原的消失;(3)细胞内铁蛋白浓度增加20倍以上。结果发现,患者的血液单核细胞在体外未分化,而是保留为未成熟的前体细胞。如果体内情况也是如此,结果可能表明获得性免疫缺陷综合征(AIDS)的病理生理学在很大程度上可能与单核细胞向巨噬细胞成熟受损的功能后果有关。