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Cross-reactive influenza virus-specific CD8+ T cells contribute to lymphoproliferation in Epstein-Barr virus-associated infectious mononucleosis.交叉反应性流感病毒特异性CD8 + T细胞促成了爱泼斯坦-巴尔病毒相关传染性单核细胞增多症中的淋巴细胞增殖。
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Newly generated CD4 T cells in aged animals do not exhibit age-related defects in response to antigen.老年动物中新生成的CD4 T细胞在对抗抗原时不会表现出与年龄相关的缺陷。
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免疫与年龄:活在过去?

Immunity and age: living in the past?

作者信息

Woodland David L, Blackman Marcia A

机构信息

Trudeau Institute, Saranac Lake, NY 12983, USA.

出版信息

Trends Immunol. 2006 Jul;27(7):303-7. doi: 10.1016/j.it.2006.05.002. Epub 2006 May 30.

DOI:10.1016/j.it.2006.05.002
PMID:16731040
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7185388/
Abstract

Increasing age is associated with a decreasing ability to mediate effective immune responses to newly encountered antigens. It is generally believed that this reflects the age-associated decline in the number, repertoire and function of available naive T cells. Here, we propose that naive T cells become increasingly irrelevant to the immune system, and that responses to newly encountered antigens are progressively dominated by cross-reactive memory T cells as the individual ages. In addition, we propose that the majority, if not all, of the response to newly encountered antigens in the elderly is mediated by cross-reactive memory T cells. This predicts highly stochastic responses to new infections that should vary between individuals, and has important implications for vaccination strategies in the elderly.

摘要

年龄增长与介导针对新遇到抗原的有效免疫反应的能力下降有关。人们普遍认为,这反映了与年龄相关的可用初始T细胞数量、库和功能的下降。在此,我们提出初始T细胞对免疫系统的相关性日益降低,并且随着个体年龄增长,对新遇到抗原的反应逐渐由交叉反应性记忆T细胞主导。此外,我们提出老年人对新遇到抗原的反应,即使不是全部,大部分也是由交叉反应性记忆T细胞介导的。这预示着对新感染的反应具有高度随机性,因人而异,并且对老年人的疫苗接种策略具有重要意义。