Department of Medicine, University of California San Diego, La Jolla, California, USA.
1] Institute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA. [2] Department of Microbiology, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
Nat Immunol. 2014 Dec;15(12):1104-15. doi: 10.1038/ni.3031.
Immunological memory is a cardinal feature of adaptive immunity and an important goal of vaccination strategies. Here we highlight advances in the understanding of the diverse T lymphocyte subsets that provide acute and long-term protection from infection. These include new insights into the transcription factors, and the upstream 'pioneering' factors that regulate their accessibility to key sites of gene regulation, as well as metabolic regulators that contribute to the differentiation of effector and memory subsets; ontogeny and defining characteristics of tissue-resident memory lymphocytes; and origins of the remarkable heterogeneity exhibited by activated T cells. Collectively, these findings underscore progress in delineating the underlying pathways that control diversification in T cell responses but also reveal gaps in the knowledge, as well as the challenges that arise in the application of this knowledge to rationally elicit desired T cell responses through vaccination and immunotherapy.
免疫记忆是适应性免疫的一个主要特征,也是疫苗接种策略的一个重要目标。在这里,我们重点介绍了对提供急性和长期抗感染保护的多种 T 淋巴细胞亚群的理解方面的进展。这包括对转录因子以及调节其与关键基因调控位点的可及性的上游“开拓性”因子的新见解,以及有助于效应和记忆亚群分化的代谢调节剂;组织驻留记忆淋巴细胞的个体发生和定义特征;以及激活 T 细胞表现出的显著异质性的起源。总的来说,这些发现强调了在描述控制 T 细胞反应多样化的潜在途径方面取得的进展,但也揭示了知识上的差距,以及在将这些知识应用于通过疫苗接种和免疫疗法理性地引发所需 T 细胞反应方面所面临的挑战。