Modeling and Remodeling the Cell: How Digital Twins and HCMV Can Elucidate the Complex Interactions of Viral Latency, Epigenetic Regulation, and Immune Responses

被引:0
作者
McMahon-Cole, Hana [1 ]
Johnson, Alicia [1 ]
Aghamiri, Sara Sadat [1 ]
Helikar, Tomas [1 ]
Crawford, Lindsey B. [1 ,2 ,3 ]
机构
[1] Univ Nebraska Lincoln, Dept Biochem, Lincoln, NE 68588 USA
[2] Nebraska Ctr Virol, Lincoln, NE 68583 USA
[3] Nebraska Ctr Integrated Biomol Commun, Lincoln, NE 68503 USA
基金
美国国家卫生研究院;
关键词
Human cytomegalovirus; Digital twin; Immune response; Latency; Epigenetics; Personalized medicine; NONHUMAN PRIMATE MODEL; HUMAN CYTOMEGALOVIRUS; HEMATOPOIETIC STEM; INFECTION;
D O I
10.1007/s40588-023-00201-w
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Purpose of ReviewHuman cytomegalovirus (HCMV), while asymptomatic in most, causes significant complications during fetal development, following transplant or in immunosuppressed individuals. The host-virus interactions regulating viral latency and reactivation and viral control of the cellular environment (immune regulation, differentiation, epigenetics) are highly complex. Understanding these processes is essential to controlling infection and can be leveraged as a novel approach for understanding basic cell biology.Recent FindingsImmune digital twins (IDTs) are digital simulations integrating knowledge of human immunology, physiology, and patient-specific clinical data to predict individualized immune responses and targeted treatments. Recent studies used IDTs to elucidate mechanisms of T cells, dendritic cells, and epigenetic control-all key to HCMV biology.Here, we discuss how leveraging the unique biology of HCMV and IDTs will clarify immune response dynamics, host-virus interactions, and viral latency and reactivation and serve as a powerful IDT-validation platform for individualized and holistic health management.
引用
收藏
页码:141 / 151
页数:11
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