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B记忆细胞可在体外被抗原刺激,从而成为分泌IgG抗体的细胞。

B-memory cells can be stimulated by antigen in vitro to become IgG antibody-secreting cells.

作者信息

North J R, Maizels R M

出版信息

Immunology. 1977 May;32(5):771-6.

Abstract

Whereas DNP-KLH primed mouse spleen cells fail to show the high IgG anti DNP levels characteristic of an anamnestic immune response when cultured for 5 days under Mishell-Dutton conditions, we show here that such a response can be observed after 8--10 days in vitro using modified Marbrook culture vessels. The kinetics of this secondary response in vitro resemble that described elsewhere for the adotpive secondary immune response in irradiated recipients, and show that insignificant numbers of IgG PFC can be expected before 6 days of culture. This timing is governed by the maturation state of B cells at the start of culture, and was not accelerated by the addition of recently boosted carrier primed spleen cells. We conclude that the deficit in IgG PFC numbers that characterizes Mishell-Dutton cultures of cells primed 2--4 months previously is due to the shortage of time during which such cultures can maintain lymphocyte division and maturation.

摘要

虽然用二硝基苯-钥孔戚血蓝蛋白(DNP-KLH)致敏的小鼠脾细胞在米谢尔-达顿(Mishell-Dutton)条件下培养5天时,未能表现出回忆性免疫反应所特有的高IgG抗DNP水平,但我们在此表明,使用改良的马尔布鲁克(Marbrook)培养容器,在体外培养8-10天后可观察到这种反应。体外这种二次反应的动力学类似于其他地方描述的受辐照受体中适应性二次免疫反应的动力学,并表明在培养6天之前,预期IgG浆细胞形成细胞(PFC)的数量很少。这个时间受培养开始时B细胞成熟状态的控制,并且不会因添加最近加强免疫的载体致敏脾细胞而加快。我们得出结论,米谢尔-达顿培养法中2-4个月前致敏的细胞所特有的IgG PFC数量不足,是由于这种培养法维持淋巴细胞分裂和成熟的时间不足所致。

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IgG response in vitro. I. The requirement for an intermediate responsive cell type.
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本文引用的文献

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