期刊
FRONTIERS IN PEDIATRICS
卷 10, 期 -, 页码 -出版社
FRONTIERS MEDIA SA
DOI: 10.3389/fped.2022.1091571
关键词
epstein-Barr virus; chronic active EBV infection; immune response; toll-like receptor; excessive inflammatory response
类别
This study aimed to investigate the immunological mechanisms of Toll-like receptor (TLR) signaling pathways in different types of Epstein-Barr virus (EBV) infection. The results showed that there was an increased expression of TLR7/TLR9 in EBV-infected patients, leading to increased downstream signaling mediators such as MyD88 and NF-κB. Particularly, in patients with chronic active EBV infection, the TLR7/TLR9 pathway was overactivated, resulting in enhanced inflammation which might be relevant to poor prognosis.
We aimed to investigate the immunological mechanisms of the Toll-like receptor (TLR) signaling pathways in different types of Epstein-Barr virus (EBV) infection. We retrospectively summarized the clinical data, routine laboratory tests and the immunological function of the infectious mononucleosis (IM) and chronic active EBV infection (CAEBV) patients. A real-time quantitative PCR array was used to detect the mRNA expression levels of TLR7/TLR9 and myeloid-differentiation factor 88 (MyD88). Flow cytometry was used to detect the protein expression of TLR7/TLR9. The MyD88 and nuclear factor-kappa B (NF-kappa B) (p65) protein were detected by western blotting. A cytometric bead array (CBA) assay was used to detect the expression of downstream cytokines. CAEBV patients presented with increased expression of TLR7/TLR9 in monocytes and B lymphocytes. TLR9 expression in the B lymphocytes of IM patients was decreased compared with the CAEBV pateints. Downstream signaling mediators, including MyD88 and NF-kappa B, were revealed to be increased in EBV-infected patients. Moreover, the expression of MyD88 and NF-kappa B was higher in CAEBV patients, leading to disrupted balance of downstream cytokines. EBV may activate the immune system via TLR7/TLR9 signaling pathways. Moreover, the overactivated TLR7/TLR9 pathway in CAEBV patients resulted in excessive inflammation, which might be relevant to the poor prognosis.
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