关键词: Enterovirus 71 Inflammation Neonatal mouse PLAC8 Th cell

Mesh : Age Factors Animals Animals, Newborn Brain / metabolism Cytokines / metabolism Disease Models, Animal Enterovirus A, Human / pathogenicity Enterovirus Infections / metabolism virology Humans Inflammation Mice Proteins / genetics metabolism RNA, Messenger / genetics T-Lymphocytes, Helper-Inducer / metabolism T-Lymphocytes, Regulatory / metabolism

来  源:   DOI:10.1016/j.virol.2021.10.001

Abstract:
Enterovirus 71 can cause severe hand, foot, and mouth disease (HFMD) in children. However, little is known about the mechanism of inflammatory disorders caused by EV71 infection and why severe cases are mainly children aged under-three. In current study, using mRNA microarray assay, the differential expression of Placenta-specific 8 (PLAC8) was identified in mice brain. In addition, we found that PLAC8 expression was down-regulated with age in mice lung tissues and human peripheral blood. Then, we further proved that PLAC8 could promote inflammation progress and disturb Th1/Th2/Th17/Treg related cytokines release after EV71 infection using PLAC8 plasmid over-expressed neonatal mouse model. Our data suggest that PLAC8 might play a crucial role in Th cell differentiation and inflammatory damage caused by EV71 infection in infants. Thus, our findings would help understand the causes of severe inflammatory injury in infants during EV71 infection, and provide new insights into the prevention and control of severe HFMD.
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