医学
外周血单个核细胞
细胞因子
免疫学
病毒
CD8型
肿瘤坏死因子α
炎症
爱泼斯坦-巴尔病毒
体外
病毒学
免疫系统
生物
生物化学
作者
Erika Onozawa,Haruna Shibayama,Ken‐Ichi Imadome,Akiho Tsuzura,Takatoshi Koyama,Osamu Miura,Ayako Arai
出处
期刊:PubMed
日期:2017-01-01
卷期号:58 (3): 189-196
被引量:9
标识
DOI:10.11406/rinketsu.58.189
摘要
In order to clarify the mechanisms underlying the development of inflammation in chronic active Epstein-Barr virus infection (CABEV), we examined cytokine production using patient samples. Eleven patients were analyzed. The serum concentrations of IFN-γ, TNF-α, and IL-6 were significantly higher in patients than in healthy donors. The mRNAs of these cytokines in peripheral blood mononuclear cells were elevated in patients as compared with healthy donors. The mRNA of IFN-γ was significantly higher in patients than in healthy donors. We examined which fraction produced the cytokines in the CD4-, CD8-, and CD56-positive fractions of PBMCs. The mRNAs of IFN-γ, TNF-α, and IL-6 were highly expressed in EBV-infected cells, whereas expression was also observed in non-infected cells. We performed in vitro infection of EBV on a T-cell line, MOLT4. EBV infection enhanced the mRNA expressions of IFN-γ and TNF-α. These results suggest that the inflammatory cytokines in CAEBV are produced not only by EBV-infected but also non-infected cells. EBV itself may have roles in the cytokine production observed in infected cells.
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