Plater-Zyberk C, Maini R N
Kennedy Institute of Rheumatology, London, U.K.
Scand J Rheumatol Suppl. 1988;75:76-83. doi: 10.3109/03009748809096744.
Using flow cytometry B lymphocytes expressing CD5 were increased in the blood of 15 out of 31 patients with rheumatoid arthritis (RA). In contrast to the monoclonal CD5+ B lymphocytes in patients with B-chronic lymphocytic leukaemia, CD5+ B cells from RA patients and neonatal cord blood are polyclonal as demonstrated by kappa/lambda expression. These B cells co-express mu and delta heavy chains and are CD19, CD20, CD21 positive. Purified CD5+ and CD5- B cells appeared of similar size and granularity as judged by light scatter values. Staphylococcus aureus C stimulated cord blood B cells showed loss of CD5 antigen following activation and production of similar amounts of IgM-rheumatoid factor (RF). EBV stimulation of purified RA B subsets lead to greater production of IgM-RF by CD5+ B cells than by CD5-B cells suggesting an enrichment of precursor cells in this fraction.
运用流式细胞术检测发现,31例类风湿关节炎(RA)患者中有15例血液中表达CD5的B淋巴细胞增多。与B慢性淋巴细胞白血病患者的单克隆CD5+B淋巴细胞不同,RA患者和新生儿脐带血中的CD5+B细胞通过κ/λ表达显示为多克隆。这些B细胞共表达μ和δ重链,且CD19、CD20、CD21呈阳性。根据光散射值判断,纯化后的CD5+和CD5-B细胞大小和颗粒度相似。金黄色葡萄球菌C刺激脐带血B细胞后,活化过程中CD5抗原丢失,并产生等量的IgM类风湿因子(RF)。EBV刺激纯化后的RA B亚群,CD5+B细胞比CD5-B细胞产生更多的IgM-RF,提示该部分中前体细胞富集。