Patel P J
J Exp Med. 1981 Sep 1;154(3):821-31. doi: 10.1084/jem.154.3.821.
Immunity to infection of mice with the facultative, intracellular pathogen Listeria monocytogenes was employed as a model system to investigate the immunological basis for the age-associated decline in anti-microbial immunity. In response to a sublethal immunizing infection, aged (24-mo old or more) mice displayed a smaller increase in spleen weight, spleen cellularity, and splenic T cell content than young (3- to 4-mo-old) mice. Aged mice also generated a smaller number of anti-Listeria protective T cells at the time of a peak response, in that their spleen cells were 1,000-fold less protective than equivalent numbers of spleen cells from the young donors, even when enriched T cell populations were employed. These results suggest that the impaired ability of aged mice to produce protective T cells is mainly responsible for decreased resistance of these mice to infection with Listeria.
以兼性细胞内病原体单核细胞增生李斯特菌感染小鼠的免疫情况作为模型系统,来研究与年龄相关的抗微生物免疫下降的免疫学基础。在应对亚致死性免疫感染时,老年(24月龄及以上)小鼠脾脏重量、脾细胞数量和脾脏T细胞含量的增加幅度小于年轻(3至4月龄)小鼠。在峰值反应时,老年小鼠产生的抗李斯特菌保护性T细胞数量也较少,因为即使使用富集的T细胞群体,其脾细胞的保护能力也比来自年轻供体的同等数量脾细胞低1000倍。这些结果表明,老年小鼠产生保护性T细胞的能力受损是导致这些小鼠对李斯特菌感染抵抗力下降的主要原因。