Nemazee David
Department of Immunology, The Scripps Research Institute, Mail Drop IMM-29, 10550 North Torrey Pines Road, La Jolla, California 92037, USA.
Nat Rev Immunol. 2006 Oct;6(10):728-40. doi: 10.1038/nri1939.
The specificities of lymphocytes for antigen are generated by a quasi-random process of gene rearrangement that often results in non-functional or autoreactive antigen receptors. Regulation of lymphocyte specificities involves not only the elimination of cells that display 'unsuitable' receptors for antigen but also the active genetic correction of these receptors by secondary recombination of the DNA. As I discuss here, an important mechanism for the genetic correction of antigen receptors is ongoing recombination, which leads to receptor editing. Receptor editing is probably an adaptation that is necessitated by the high probability of receptor autoreactivity. In both B cells and T cells, the genes that encode the two chains of the antigen receptor seem to be specialized to promote, on the one hand, the generation of diverse specificities and, on the other hand, the regulation of these specificities through efficient editing.
淋巴细胞对抗原的特异性是由基因重排的准随机过程产生的,这一过程常常导致无功能或自身反应性的抗原受体。淋巴细胞特异性的调节不仅涉及消除那些对抗原显示出“不合适”受体的细胞,还涉及通过DNA的二次重组对这些受体进行主动的基因校正。正如我在此所讨论的,抗原受体基因校正的一个重要机制是正在进行的重组,这会导致受体编辑。受体编辑可能是一种适应,这是由受体自身反应性的高概率所必需的。在B细胞和T细胞中,编码抗原受体两条链的基因似乎专门用于一方面促进多样特异性的产生,另一方面通过高效编辑来调节这些特异性。