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Somatic mutation of immunoglobulin VH6 genes in human infants

机译:婴儿免疫球蛋白VH6基因的体细胞突变

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摘要

Infants respond to antigen by making antibody that is generally of low affinity for antigen. Somatic hypermutation of immunoglobulin genes, and selection of cells expressing mutations with improved affinity for antigen, are the molecular and cellular processes underlying the maturation of antibody affinity. We have reported previously that neonates and infants up to 2 months of age, including individuals undergoing strong immunological challenge, show very few mutated VH6 sequences, with low mutation frequencies in mutated sequences, and little evidence of selection. We have now examined immunoglobulin genes from healthy infants between 2 and 10 months old for mutation and evidence of selection. In this age group, the proportion of VH6 sequences which are mutated and the mutation frequency in mutated sequences increase with age. There is evidence of selection from 6 months old. These results indicate that the process of affinity maturation, which depends on cognate T–B cell interaction and functional germinal centres, is approaching maturity from 6 months old.
机译:婴儿通过制备对抗原的亲和力通常较低的抗体来对抗原作出反应。免疫球蛋白基因的体细胞超突变以及表达对抗原亲和力提高的突变的细胞的选择是抗体亲和力成熟的分子和细胞过程。我们以前曾报道过,新生儿和2月龄以下的婴儿,包括经历强免疫学攻击的个体,显示出很少的VH6突变序列,突变序列中的突变频率低,并且没有选择的证据。现在,我们已经检查了2到10个月大的健康婴儿的免疫球蛋白基因的突变和选择证据。在这个年龄组中,随着年龄的增长,突变的VH6序列的比例和突变序列中的突变频率都会增加。有选择从6个月大开始的证据。这些结果表明,依赖于关联的T–B细胞相互作用和功能生发中心的亲和力成熟过程已从6个月大开始接近成熟。

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