Rethinking human cytomegalovirus latency reservoir

被引:10
|
作者
Schwartz, Michal [1 ]
Stern-Ginossar, Noam [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Genet, Rehovot, Israel
基金
欧盟地平线“2020”;
关键词
cytomegalovirus; latency; myeloid cells; reactivation; MURINE CYTOMEGALOVIRUS; GENE-EXPRESSION; T-CELLS; INFECTION; REPLICATION; REACTIVATION; PERSISTENCE; SPLEEN; SITE; DNA;
D O I
10.1111/nyas.14994
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Human cytomegalovirus (HCMV) is a prevalent herpesvirus, infecting the majority of the human population. Like other herpesviruses, it causes lifelong infection through the establishment of latency. Although reactivation from latency can cause significant morbidity and mortality in immunocompromised hosts, our understanding of HCMV latency and how it is maintained remains limited. Here, we discuss the characterized latency reservoir in hematopoietic cells in the bone marrow and the gaps in our knowledge of mechanisms that facilitate HCMV genome maintenance in dividing cells. We further review clinical evidence that strongly suggests the tissue origin of HCMV reactivation, and we outline similarities to murine cytomegalovirus where latency in tissue-resident cells has been demonstrated. Overall, we think these observations call for a rethinking of HCMV latency reservoirs and point to potential sources of HCMV latency that reside in tissues.
引用
收藏
页码:30 / 36
页数:7
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