Wang Clifford L, Wabl Matthias
Department of Microbiology and Immunology, University of California, San Francisco, CA 94143, USA.
J Immunol. 2004 May 15;172(10):5815-21. doi: 10.4049/jimmunol.172.10.5815.
Small resting B lymphocytes all start out producing IgM Abs. Upon encountering Ag, the cells become activated and make a switch from IgM to other Ig classes. This class switch serves to distribute a particular V region to different Ig C regions. Each C region mediates a specialized effector function, and so, through switching, an organism can guide its Abs to various sites. Creating the new H chain requires loop-out and deletion of DNA between switch regions. These DNA acrobatics require transcription of the switch regions, presumably so that necessary factors can gain access to the DNA. These requisite switching factors include activation-induced cytidine deaminase and components of general DNA repair, including base excision repair, mismatch repair, and double-strand break repair. Despite much recent progress, not all important factors have been discovered, especially those that may guide recombination to a particular subclass.
静止的小B淋巴细胞最初都产生IgM抗体。遇到抗原后,这些细胞被激活,并从IgM转换为其他Ig类别。这种类别转换用于将特定的V区分配到不同的Ig C区。每个C区介导一种特殊的效应功能,因此,通过转换,生物体可以将其抗体导向不同的部位。产生新的重链需要环出并删除转换区之间的DNA。这些DNA的变化需要转换区的转录,大概是为了使必要的因子能够接触到DNA。这些必需的转换因子包括激活诱导的胞嘧啶脱氨酶和一般DNA修复的成分,包括碱基切除修复、错配修复和双链断裂修复。尽管最近取得了很大进展,但并非所有重要因子都已被发现,特别是那些可能引导重组到特定亚类的因子。