Tissue Analysis Core, Immunology laboratory, Vaccine Research Center, NIAID, NIH, Bethesda, Maryland, USA.
Curr Opin HIV AIDS. 2018 Mar;13(2):112-118. doi: 10.1097/COH.0000000000000437.
To describe recent findings on the effect of HIV/SIV infection on lymph node viral and T-cell dynamics using imaging-based methodologies.
Chronic infection, particularly HIV/SIV, alters dramatically the microenvironment, immune cell frequency, distribution, function and tissue organization of secondary lymphoid tissues. These changes are not always reversible. Over the past few years, the implementation of advanced imaging protocols on human lymph node biopsies as well as on longitudinal lymphoid tissues samples from nonhuman primates (NHP) have provided a wealth of information on how local immune responses evolve over time in response to a persisting retroviral pathogen. Most of the information concerns cytotoxic and helper T cells and viral dynamics. In this review, we detail this information focusing on HIV/SIV infection. We also comment on the gaps that imaging technologies have bridged in our understanding and discuss the translational value of these new findings in the light of emerging therapeutic agendas.
Novel imaging platforms allow for dissecting the spatiotemporal dynamics of immune interactions further improving our understanding of the interplay between virus and host and providing important information for designing successful preventive and curative strategies.
描述利用基于成像的方法研究 HIV/SIV 感染对淋巴结病毒和 T 细胞动力学影响的最新发现。
慢性感染,特别是 HIV/SIV,极大地改变了次级淋巴组织的微环境、免疫细胞频率、分布、功能和组织结构。这些变化并非总是可逆的。在过去的几年中,在人类淋巴结活检以及非人类灵长类动物(NHP)的纵向淋巴组织样本上实施先进的成像方案,提供了大量信息,说明局部免疫反应如何随着时间的推移针对持续存在的逆转录病毒病原体而演变。大多数信息涉及细胞毒性和辅助性 T 细胞以及病毒动力学。在这篇综述中,我们详细介绍了这些信息,重点关注 HIV/SIV 感染。我们还评论了成像技术在我们的理解中弥合的差距,并根据新出现的治疗方案讨论了这些新发现的转化价值。
新型成像平台允许进一步剖析免疫相互作用的时空动态,从而提高我们对病毒和宿主相互作用的理解,并为设计成功的预防和治疗策略提供重要信息。