Petersen J, Heilmann C, Bjerrum O J, Ingemann-Hansen T, Halkjaer-Kristensen J
Scand J Immunol. 1983 May;17(5):471-8. doi: 10.1111/j.1365-3083.1983.tb00814.x.
A haemolytic plaque-forming cell (PFC) assay detecting human B lymphocytes secreting IgG rheumatoid factor (RF) was established using sheep erythrocytes (SRBC) sensitized with rabbit IgG, developing rabbit anti-human IgG, and complement. IgG-RF PFC were only demonstrated with IgG-depleted guinea-pig serum as the source of complement. Cells spontaneously secreting IgG-RF were found among synovial fluid mononuclear cells (mean, 134/10(6)) and synovial tissue mononuclear cells (mean, 1775/10(6)) from patients with rheumatoid arthritis, whereas few were recorded among blood lymphocytes (mean, 3/10(6)). The experiments revealed that the RF-IgG PFC were protein-synthesizing B lymphocytes. The antibody specificity of the secreted IgF-RF was verified by the inhibitory effect of exogenous human and rabbit IgG on PFC formation.
利用用兔IgG致敏的绵羊红细胞(SRBC)、兔抗人IgG和补体建立了一种检测分泌IgG类风湿因子(RF)的人B淋巴细胞的溶血空斑形成细胞(PFC)试验。仅用IgG缺失的豚鼠血清作为补体来源时才能证明IgG-RF PFC的存在。在类风湿性关节炎患者的滑液单核细胞(平均134/10⁶)和滑膜组织单核细胞(平均1775/10⁶)中发现了自发分泌IgG-RF的细胞,而在血液淋巴细胞中记录到的此类细胞很少(平均3/10⁶)。实验表明,RF-IgG PFC是蛋白质合成B淋巴细胞。外源性人IgG和兔IgG对PFC形成的抑制作用证实了分泌的IgF-RF的抗体特异性。