Chen Z C, Radic M Z, Galili U
Department of Cardiovascular-Thoracic Surgery, Rush University, 1653 West Congress Parkway, Chicago, IL 60612, USA.
Mol Immunol. 2000 Jun;37(8):455-66. doi: 10.1016/s0161-5890(00)00064-x.
This study analyzes the gene repertoire coding for antibodies to an evolutionary novel immunogenic carbohydrate antigen in mice. The alpha-gal epitope (Gal alpha 1-3Gal beta 1-4GlcNAc-R) is an autoantigen, abundantly expressed in wild type mice, but absent in alpha 1,3galactosyltransferase knock-out (KO) mice, where it can induce the production of the anti-Gal antibody. Hybridoma clones secreting anti-Gal were isolated from different mice and their immunoglobulin genes were analyzed. All anti-Gal clones were found to be encoded by the heavy chain gene VH22.1 and light chain gene VK5.1. Moreover, one 'forbidden' anti-Gal clone, produced in a wild type mouse, was also encoded by VH 22.1 and VK 5.1. The genes coding for the different anti-Gal clones were found to contain somatic mutations and different CDR3 domains. These data imply that a highly restricted gene usage combined with junctional diversity and somatic mutations can generate new antibodies that have not been produced in the course of the evolution of a species.
本研究分析了编码小鼠中针对一种进化上新型免疫原性碳水化合物抗原的抗体的基因库。α-半乳糖表位(Galα1-3Galβ1-4GlcNAc-R)是一种自身抗原,在野生型小鼠中大量表达,但在α1,3-半乳糖基转移酶敲除(KO)小鼠中不存在,在KO小鼠中它可诱导抗Gal抗体的产生。从不同小鼠中分离出分泌抗Gal的杂交瘤克隆,并对其免疫球蛋白基因进行分析。发现所有抗Gal克隆均由重链基因VH22.1和轻链基因VK5.1编码。此外,在野生型小鼠中产生的一个“禁忌”抗Gal克隆也由VH 22.1和VK 5.1编码。发现编码不同抗Gal克隆的基因含有体细胞突变和不同的互补决定区3(CDR3)结构域。这些数据表明,高度受限的基因使用与连接多样性和体细胞突变相结合,可以产生在物种进化过程中未曾产生过的新抗体。