Haaijman J J, Schuit H R, Hijmans W
Immunology. 1977 Apr;32(4):427-34.
The number of cells containing cytoplasmic immunoglobulin (C-Ig cells) was determined in the spleen, mesenteric lymph nodes, bone marrow and Peyer's patches of CBA mice of different ages. A rapid increase in the number of C-Ig cells at between 2 and 6 weeks of age was observed in spleen and gut-associated lymphoid organs. The absolute number of C-Ig cells in these organs decreases with advancing age. In the bone marrow, the number of C-Ig cells increases steadily with age up to one year. From one year on, the number remains approximately constant in the males. In female mice, the number of C-Ig cells, mainly of the IgA class, increases sharply around 1 year of age. The spleen is the major site of Ig synthesis up to about 6 months of age. In older animals, the relative contribution of the bone marrow increases with age, possibly due to a gradual shift in the individual animal from primary type responses to a pattern of secondary type responses. No indication of a decreased overall immunological activity in senescence was obtained.
测定了不同年龄CBA小鼠脾脏、肠系膜淋巴结、骨髓和派尔集合淋巴结中含细胞质免疫球蛋白的细胞(C-Ig细胞)数量。在脾脏和肠道相关淋巴器官中,观察到2至6周龄时C-Ig细胞数量迅速增加。这些器官中C-Ig细胞的绝对数量随年龄增长而减少。在骨髓中,C-Ig细胞数量随年龄稳步增加,直至1岁。从1岁起,雄性小鼠的数量大致保持恒定。在雌性小鼠中,主要为IgA类的C-Ig细胞数量在约1岁时急剧增加。脾脏是约6个月龄前Ig合成的主要部位。在老年动物中,骨髓的相对贡献随年龄增加,这可能是由于个体动物从初级反应模式逐渐转变为次级反应模式。未发现衰老过程中整体免疫活性降低的迹象。