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TLR2 Expression in Peripheral CD4+ T Cells Promotes Th17 Response and Is Associated with Disease Aggravation of Hepatitis B Virus-Related Acute-On-Chronic Liver Failure

机译:TLR2在外周CD4 + T细胞中的表达促进Th17反应并与乙型肝炎病毒相关的慢性肝功能衰竭相关的疾病加重

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摘要

Th17 responses have been shown to play crucial roles in the pathogenesis of hepatitis B virus (HBV)-associated acute-on-chronic liver failure (ACLF). The mechanism underlying the enhanced Th17 responses in these patients remains largely unclear. Here we investigated toll-like receptors (TLRs) expression in peripheral T cells and their roles in Th17 cell differentiation and disease aggravation in ACLF patients. 18 healthy subjects (HS), 20 chronic HBV-infected (CHB) patients, and 26 ACLF patients were enrolled and examined for TLRs expression in peripheral blood mononuclear cells (PBMCs). The correlations of T cell TLR2 expression with the antigen non-specific Th17 responses and disease aggravation, as well as the Th17 response to TLR2 ligand stimulation were evaluated in ACLF patients. Compared to HS and CHB patients, ACLF patients showed a distinct TLRs expression pattern in PBMCs. Significantly increased TLR2 expression in T cells was observed in ACLF patients. The TLR2 expression in CD4+ T cells was correlated with the Th17 responses and the clinical markers for disease aggravation in ACLF patients. Moreover, TLR2 ligands stimulation promoted Th17 cell differentiation and response in PBMCs of ACLF patients. These findings implicate that TLR2 signaling plays critical roles in Th17 cell differentiation and disease aggravation of HBV-related ACLF.
机译:Th17反应已显示在乙型肝炎病毒(HBV)相关的慢性慢性肝衰竭(ACLF)的发病机理中起关键作用。这些患者中Th17反应增强的潜在机制仍不清楚。在这里,我们研究了ACLF患者外周T细胞中Toll样受体(TLR)的表达及其在Th17细胞分化和疾病加重中的作用。招募了18位健康受试者(HS),20位慢性HBV感染(CHB)患者和26位ACLF患者,并检查了外周血单核细胞(PBMC)中的TLRs表达。在ACLF患者中评估了T细胞TLR2表达与抗原非特异性Th17反应和疾病加重以及Th17对TLR2配体刺激的反应之间的相关性。与HS和CHB患者相比,ACLF患者在PBMC中显示出不同的TLRs表达模式。在ACLF患者中观察到T细胞中TLR2表达显着增加。 CD4 + T细胞中TLR2的表达与ACLF患者Th17反应和疾病加重的临床标志物相关。此外,TLR2配体刺激可促进ACLF患者PBMC中Th17细胞的分化和应答。这些发现暗示TLR2信号在Th17细胞分化和HBV相关ACLF的疾病加重中起关键作用。

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