Emory Vaccine Center, Emory University, 1462 Clifton Road, Atlanta, GA, 30322, USA.
Immunol Cell Biol. 2011 Mar;89(3):340-5. doi: 10.1038/icb.2010.155. Epub 2011 Feb 8.
Live virus vaccines provide a unique opportunity to study human CD8(+) T-cell memory in the context of a controlled, primary acute viral infection. Yellow fever virus-17D and Dryvax are two such live-virus vaccines that are highly efficacious, used worldwide and provide long-term immunity against yellow fever and smallpox respectively. In this review, we describe the properties of virus-specific memory CD8(+) T cells generated in smallpox and yellow fever vaccinees. We address fundamental questions regarding magnitude, functional quality and longevity of the CD8(+) T-cell response, which are otherwise challenging to address in humans. These findings provide insights into the attributes of the human immune system as well as provide a benchmark for the optimal quality of a CD8(+) T-cell response that can be used to evaluate novel candidate vaccines.
活病毒疫苗为在受控的原发性急性病毒感染背景下研究人类 CD8(+)T 细胞记忆提供了独特的机会。黄热病病毒 17D 和 Dryvax 是两种活病毒疫苗,它们具有高度的功效,在全球范围内使用,并分别提供针对黄热病和天花的长期免疫力。在这篇综述中,我们描述了在天花和黄热病疫苗接种者中产生的针对病毒特异性记忆 CD8(+)T 细胞的特性。我们解决了关于 CD8(+)T 细胞反应的大小、功能质量和持久性的基本问题,这些问题在人类中难以解决。这些发现为人类免疫系统的属性提供了深入的了解,并为可以用于评估新型候选疫苗的 CD8(+)T 细胞反应的最佳质量提供了基准。