Goulding N J, Eales L J, Hall N D
Ann Rheum Dis. 1986 Nov;45(11):925-31. doi: 10.1136/ard.45.11.925.
Mononuclear cells expressing Fc gamma receptors that form Facb rosettes are increased in the peripheral blood of patients with rheumatoid arthritis compared with controls. Healthy individuals with a positive skin response to tuberculin showed a marked increase in numbers of circulating Facb-R+ cells three days after challenge, returning to baseline after seven days. No response was observed in subjects showing a negative skin test. A similar increase in Facb-R+ cell numbers was measured after intramuscular injection of another specific antigen, tetanus toxoid. In addition to this enhancement of Facb-R+ cell numbers, evidence has been obtained that these cells are in an activated state postimmunisation as judged by acquisition of low density and increased expression of class II MHC antigens. Apparently identical changes in Facb-R+ cell numbers and activation may be induced in vitro either by culturing sensitised mononuclear cells with specific antigen for three days or by an overnight incubation of normal cells with gamma-interferon (gamma-IFN). By analogy, therefore, the increased numbers of Facb-R+ cells in patients with rheumatoid arthritis are probably induced by gamma-interferon generated as part of an antigen driven immune response. In this context it is interesting that patients with Felty's syndrome, in whom neutropenia increases susceptibility to infections leading to the possibility of further stimulation of the immune system by micro-organisms, have particularly high levels of circulating Facb-R+ cells.
与对照组相比,类风湿性关节炎患者外周血中表达形成Facb玫瑰花结的Fcγ受体的单核细胞增多。对结核菌素皮肤反应呈阳性的健康个体在激发后三天循环中的Facb-R+细胞数量显著增加,七天后恢复至基线水平。皮肤试验呈阴性的受试者未观察到反应。肌肉注射另一种特异性抗原破伤风类毒素后,也检测到Facb-R+细胞数量有类似增加。除了Facb-R+细胞数量增加外,还获得证据表明,根据低密度的获得和II类MHC抗原表达的增加判断,这些细胞在免疫后处于激活状态。通过用特异性抗原培养致敏单核细胞三天或用γ干扰素(γ-IFN)过夜孵育正常细胞,在体外可能诱导Facb-R+细胞数量和激活发生明显相同的变化。因此,类推而言,类风湿性关节炎患者中Facb-R+细胞数量增加可能是由作为抗原驱动免疫反应一部分产生的γ干扰素诱导的。在这种情况下,有意思的是,费尔蒂综合征患者循环中的Facb-R+细胞水平特别高,在这些患者中,中性粒细胞减少会增加感染易感性,导致微生物进一步刺激免疫系统的可能性。