van Dijk-Härd I, Söderström I, Feld S, Holmberg D, Lundkvist I
Division for Clinical Immunology, Karolinska Institute, Huddinge Hospital, Sweden.
Eur J Immunol. 1997 Jun;27(6):1381-6. doi: 10.1002/eji.1830270613.
To elucidate the basic molecular events underlying humoral immunity during ontogeny and senescence, we analyzed a panel of 179 polymerase chain reaction-derived VH6-D-JH rearrangements from cord blood, peripheral blood, and spleen. Nucleotide sequence analysis of the CDR3 region shows that there is a difference in D and JH gene usage in functional rearrangements between lymphocytes from peripheral blood and spleen. Analysis of the VH6 gene shows that the mutational frequencies rise from 0.81% in cord blood to 1.96% in peripheral blood lymphocytes derived from young adults, and decrease to 0.80% in samples from individuals older than 50 years. The number of rearrangements carrying mutations follows a similar pattern: 22% in cord blood, 73% in the age group 20-49 years, and 57% in the age group over 50 years. The mutational frequencies among the mutated genes are, however, similar for cord blood and young adults, 2.76% and 2.51%, respectively, and 1.3% in older adults. These data show an age-related impaired affinity maturation which might relate to the decrease in immunological responsiveness among the elderly.
为阐明个体发育和衰老过程中体液免疫潜在的基本分子事件,我们分析了来自脐带血、外周血和脾脏的179个聚合酶链反应衍生的VH6-D-JH重排。CDR3区域的核苷酸序列分析表明,外周血和脾脏淋巴细胞功能性重排中D和JH基因的使用存在差异。VH6基因分析显示,突变频率从脐带血中的0.81%上升到年轻成年人外周血淋巴细胞中的1.96%,在50岁以上个体的样本中降至0.80%。携带突变的重排数量遵循类似模式:脐带血中为22%,20-49岁年龄组中为73%,50岁以上年龄组中为57%。然而,突变基因中的突变频率在脐带血和年轻成年人中相似,分别为2.76%和2.51%,在老年人中为1.3%。这些数据显示了与年龄相关的亲和力成熟受损,这可能与老年人免疫反应性降低有关。