How cytokines control immunoglobulin class switching.

Behring Institute Mitteilungen Pub Date : 1995-06-01
M Lorenz, S Jung, A Radbruch
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Abstract

B lymphocytes can alter the class of antibody they produce by immunoglobulin class switch recombination. This recombination is targeted by distinct cytokines to particular switch regions. Prior to switch recombination, the same cytokines induce transcription through the targeted switch regions and generate IH "switch" transcripts. To show whether the two events are functionally related, we have replaced the endogenous interleukin-4 (IL-4) dependent promoter of murine I gamma 1 switch transcripts by an heterologous promoter, the human metallothionein IIA (hMT) promoter. Indeed, switch recombination can be targeted to IgG1 by the hMT promoter. In mutant mice, which cannot generate processed switch transcripts, switch recombination cannot be targeted to IgG1 by the hMT promoter. Thus, IL-4 targets switch recombination to IgG1 by induction of processed switch transcripts.

细胞因子如何控制免疫球蛋白类转换。
B淋巴细胞可以通过免疫球蛋白类开关重组改变其产生的抗体类别。这种重组是由不同的细胞因子针对特定的开关区域。在开关重组之前,相同的细胞因子通过目标开关区域诱导转录并产生IH“开关”转录本。为了证明这两个事件是否在功能上相关,我们用一个异源启动子,即人金属硫蛋白IIA (hMT)启动子取代了内源性白细胞介素-4 (IL-4)依赖的小鼠I γ 1开关转录本启动子。事实上,开关重组可以通过hMT启动子靶向IgG1。在突变小鼠中,不能产生加工过的开关转录物,开关重组不能通过hMT启动子靶向IgG1。因此,IL-4靶标通过诱导加工过的开关转录物将重组开关转换为IgG1。
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