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Epstein-Barr Virus and miRNAs: Partners in Crime in the Pathogenesis of Multiple Sclerosis?
被引:19
|作者:
Hassani, Asma
[1
]
Khan, Gulfaraz
[1
]
机构:
[1] United Arab Emirates Univ, Dept Microbiol & Immunol, Coll Med & Hlth Sci, Al Ain, U Arab Emirates
来源:
FRONTIERS IN IMMUNOLOGY
|
2019年
/
10卷
关键词:
miRNA;
post-transcriptional regulation;
multiple sclerosis;
EBV;
immune response;
INFECTIOUS-MONONUCLEOSIS;
T-CELLS;
REGULATORY NETWORK;
MICRORNAS TARGET;
RISK;
EBV;
BIOGENESIS;
IDENTIFICATION;
EXPRESSION;
RECOGNITION;
D O I:
10.3389/fimmu.2019.00695
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
MicroRNAs (miRNAs) are small non-coding RNAs that modulate gene expression post transcriptionally. In healthy individuals, miRNAs contribute to maintaining gene expression homeostasis. However, the level of miRNAs expressed is markedly altered in different diseases, including multiple sclerosis (MS). The impact of such changes is being investigated, and thought to shape the immune system into the in fl ammatory autoimmune phenotype. Much is yet to be learned about the contribution of miRNAs in the molecular pathology of MS. Epstein-Barr virus (EBV) infection is a major risk factor for the development of MS. EBV encodes more than 40 miRNAs, most of which have been studied in the context of EBV associated cancers. These viral miRNAs regulate genes involved in cell apoptosis, antigen presentation and recognition, as well as B cell transformation. If EBV infection contributes to the pathology of MS, it is plausible that EBV miRNAs may be involved. Unfortunately, there are limited studies addressing how EBV miRNAs are involved in the pathogenesis of MS. This review summarizes what has been reported regarding cellular and viral miRNA pro fi les in MS and proposes possible interactions between the two in the development of MS.
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页数:9
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