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在人巨细胞病毒的裂解和潜伏感染中,T 细胞反应的产生、维持和组织分布。

Generation, maintenance and tissue distribution of T cell responses to human cytomegalovirus in lytic and latent infection.

机构信息

Division of Infectious Diseases, Department of Medicine, University of Cambridge, Addenbrookes Hospital, Level 5, Hills Road, Box 157, Cambridge, CB2 0QQ, UK.

出版信息

Med Microbiol Immunol. 2019 Aug;208(3-4):375-389. doi: 10.1007/s00430-019-00598-6. Epub 2019 Mar 20.

DOI:10.1007/s00430-019-00598-6
PMID:30895366
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6647459/
Abstract

Understanding how the T cell memory response directed towards human cytomegalovirus (HCMV) develops and changes over time while the virus persists is important. Whilst HCMV primary infection and periodic reactivation is well controlled by T cell responses in healthy people, when the immune system is compromised such as post-transplantation, during pregnancy, or underdeveloped such as in new-born infants and children, CMV disease can be a significant problem. In older people, HCMV infection is associated with increased risk of mortality and despite overt disease rarely being seen there are increases in HCMV-DNA in urine of older people suggesting that there is a change in the efficacy of the T cell response following lifelong infection. Therefore, understanding whether phenomenon such as "memory inflation" of the immune response is occurring in humans and if this is detrimental to the overall health of individuals would enable the development of appropriate treatment strategies for the future. In this review, we present the evidence available from human studies regarding the development and maintenance of memory CD8 + and CD4 + T cell responses to HCMV. We conclude that there is only limited evidence supportive of "memory inflation" occurring in humans and that future studies need to investigate immune cells from a broad range of human tissue sites to fully understand the nature of HCMV T cell memory responses to lytic and latent infection.

摘要

了解针对人巨细胞病毒 (HCMV) 的 T 细胞记忆反应如何随着时间的推移而发展和变化,同时病毒持续存在,这一点很重要。虽然 HCMV 原发性感染和周期性再激活在健康人群中被 T 细胞反应很好地控制,但当免疫系统受损时,如移植后、怀孕期间,或在新生儿和儿童等发育不全时,CMV 疾病可能是一个重大问题。在老年人中,HCMV 感染与死亡率增加有关,尽管很少出现显性疾病,但老年人尿液中 HCMV-DNA 增加表明,随着终身感染,T 细胞反应的效力发生了变化。因此,了解人类是否会出现免疫反应的“记忆膨胀”等现象,以及这种现象是否对个体的整体健康有害,将能够为未来制定适当的治疗策略。在这篇综述中,我们介绍了来自人类研究的关于 HCMV 记忆 CD8+和 CD4+T 细胞反应的发展和维持的现有证据。我们得出结论,只有有限的证据支持人类发生“记忆膨胀”,未来的研究需要从广泛的人类组织部位调查免疫细胞,以充分了解 HCMV 裂解和潜伏感染的 T 细胞记忆反应的性质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/6647459/f30417d42f86/430_2019_598_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/6647459/e68c25e6aee8/430_2019_598_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/6647459/c8861ba12309/430_2019_598_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/6647459/d0dac552acf1/430_2019_598_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/6647459/eb4bc73f2a0a/430_2019_598_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/6647459/f30417d42f86/430_2019_598_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/6647459/e68c25e6aee8/430_2019_598_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/6647459/c8861ba12309/430_2019_598_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/6647459/d0dac552acf1/430_2019_598_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/6647459/eb4bc73f2a0a/430_2019_598_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0252/6647459/f30417d42f86/430_2019_598_Fig5_HTML.jpg

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