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重组白细胞介素2和γ干扰素在体外人B细胞终末成熟的不同阶段发挥协同作用。

Recombinant interleukin 2 and gamma-interferon act synergistically on distinct steps of in vitro terminal human B cell maturation.

作者信息

Fauci A S

出版信息

J Clin Invest. 1986 Apr;77(4):1173-9. doi: 10.1172/JCI112418.

Abstract

The effects of recombinant interleukin 2 (IL-2) on the in vitro differentiation of human tonsillar B cells which were not preincubated with Staphylococcus aureus Cowan I or with anti-human IgM were investigated. IL-2 was shown to induce the generation of Ig-containing cells in a dose-dependent fashion from 2.5 to 2,500 U IL-2/ml. Conversely, the quantities of Ig secreted in the culture supernatant were found in the majority of experiments to peak at 25 U/ml. The possible presence, in cultures stimulated with IL-2, of cells that were capable of synthesizing Ig but that did not secrete the Ig they have produced was investigated. Among a number of factors tested, we found that gamma-interferon, which did not trigger in vitro B cell differentiation when used alone, can induce an increased secretion of Ig without noticeable change in the number of Ig-containing cells in cultures stimulated with IL-2. The possibility that gamma-interferon and IL-2 act on subsequent steps of in vitro B cell differentiation is discussed.

摘要

研究了重组白细胞介素2(IL-2)对未预先用金黄色葡萄球菌Cowan I或抗人IgM孵育的人扁桃体B细胞体外分化的影响。结果显示,IL-2以剂量依赖方式诱导含Ig细胞的生成,IL-2浓度范围为2.5至2500 U/ml。相反,在大多数实验中发现,培养上清液中分泌的Ig量在25 U/ml时达到峰值。研究了在用IL-2刺激的培养物中,是否存在能够合成Ig但不分泌所产生Ig的细胞。在测试的多种因素中,我们发现γ干扰素单独使用时不会触发体外B细胞分化,但它可以在IL-2刺激的培养物中诱导Ig分泌增加,而含Ig细胞数量无明显变化。讨论了γ干扰素和IL-2作用于体外B细胞分化后续步骤的可能性。

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