Lau L L, Jamieson B D, Somasundaram T, Ahmed R
Department of Microbiology and Immunology, UCLA School of Medicine 90024.
Nature. 1994 Jun 23;369(6482):648-52. doi: 10.1038/369648a0.
Memory is a hallmark of the immune system and ever since its recognition there has been considerable interest in understanding how immunity is maintained. The current model is that long-term memory is dependent on persistent antigenic stimulation. We report here results that challenge this view and provide evidence that antigen is not essential for the maintenance of CD8+ T-cell memory. We show that memory CD8+ cytotoxic T lymphocytes persist indefinitely in the absence of priming antigen, retain the memory phenotype (CD44hi), and provide protection against virus challenge. These findings suggest a re-evaluation of our current thinking on mechanisms involved in maintaining immunity and have implications towards designing effective vaccination strategies.
记忆是免疫系统的一个标志,自从它被发现以来,人们对理解免疫如何维持一直有着浓厚的兴趣。目前的模型认为长期记忆依赖于持续的抗原刺激。我们在此报告的结果对这一观点提出了挑战,并提供证据表明抗原对于维持CD8+ T细胞记忆并非必不可少。我们表明,记忆性CD8+ 细胞毒性T淋巴细胞在没有起始抗原的情况下可无限期持续存在,保留记忆表型(CD44高表达),并提供针对病毒攻击的保护作用。这些发现提示我们需要重新评估目前关于维持免疫机制的认识,并对设计有效的疫苗接种策略具有启示意义。