Factors Affecting the Immunity to Respiratory Syncytial Virus: From Epigenetics to Microbiome

被引:43
|
作者
Fonseca, Wendy [1 ]
Lukacs, Nicholas W. [1 ,2 ]
Ptaschinski, Catherine [1 ,2 ]
机构
[1] Univ Michigan, Dept Pathol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Mary H Weiser Food Allergy Ctr, Ann Arbor, MI 48109 USA
来源
FRONTIERS IN IMMUNOLOGY | 2018年 / 9卷
基金
美国国家卫生研究院;
关键词
respiratory syncytial virus; neonatal immunity; epigenetics; microbiome; metabolites; CD4(+) T-CELLS; PLACEBO-CONTROLLED TRIAL; TOBACCO-SMOKE EXPOSURE; TNF-ALPHA PRODUCTION; IFN-GAMMA PROMOTER; HUMAN CORD-BLOOD; DNA METHYLATION; RISK-FACTORS; RSV BRONCHIOLITIS; CHILDHOOD ASTHMA;
D O I
10.3389/fimmu.2018.00226
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Respiratory syncytial virus (RSV) is a common pathogen that infects virtually all children by 2 years of age and is the leading cause of hospitalization of infants worldwide. While most children experience mild symptoms, some children progress to severe lower respiratory tract infection. Those children with severe disease have a much higher risk of developing childhood wheezing later in life. Many risk factors are known to result in exacerbated disease, including premature birth and early age of RSV infection, when the immune system is relatively immature. The development of the immune system before and after birth may be altered by several extrinsic and intrinsic factors that could lead to severe disease predisposition in children who do not exhibit any currently known risk factors. Recently, the role of the microbiome and the resulting metabolite profile has been an area of intense study in the development of lung disease, including viral infection and asthma. This review explores both known risk factors that can lead to severe RSV-induced disease as well as emerging topics in the development of immunity to RSV and the long-term consequences of severe infection.
引用
收藏
页数:15
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