Deregulation of immune response contributing to fulminant hepatitis in HEV infected pregnant women

Author:

Liang Yining12,Zhang Jiayue3,Luo Dehong2,Cheng Lixin4,Wang Yijin1ORCID,

Affiliation:

1. School of Medicine Southern University of Science and Technology Shenzhen Guangdong China

2. Department of Radiology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital Chinese Academy of Medical Sciences and Peking Union Medical College Shenzhen Guangdong China

3. School of Pharmacy Jiangsu Food & Pharmaceutical Science College Huaian Jiangsu China

4. School of Medicine Shenzhen People's Hospital, First Affiliated Hospital of Southern University of Science and Technology, Second Clinical Medicine College of Jinan University Shenzhen Guangdong China

Abstract

AbstractHepatitis E virus (HEV) infection in pregnant women is associated with a wide spectrum of adverse consequences for both mother and fetus. The high mortality in this population appears to be associated with hormonal changes and consequent immunological changes. This study conducted an analysis of immune responses in pregnant women infected with HEV manifesting varying severity. Data mining analysis of the GSE79197 was utilized to examine differentially biological functions in pregnant women with HEV infection (P‐HEV) versus without HEV infection (P‐nHEV), P‐HEV progressing to ALF (P‐ALF) versus P‐HEV, and P‐HEV versus non‐pregnant women with HEV infection (nP‐HEV). We found cellular response to interleukin and immune response‐regulating signalings were activated in P‐HEV compared with P‐nHEV. However, there was a significant decrease of immune responses, such as T cell activation, leukocyte cell‐cell adhesion, regulation of lymphocyte activation, and immune response‐regulating signaling pathway in P‐ALF patient than P‐HEV patient. Compared with nP‐HEV, MHC protein complex binding function was inhibited in P‐HEV. Further microRNA enrichment analysis showed that MAPK and T cell receptor signaling pathways were inhibited in P‐HEV compared with nP‐HEV. In summary, immune responses were activated during HEV infection while being suppressed when developing ALF during pregnancy, heightening the importance of immune mediation in the pathogenesis of severe outcome in HEV infected pregnant women.

Publisher

Wiley

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