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Tim-3 expression on peripheral monocytes and CD3+CD16/CD56+natural killer-like T cells in patients with chronic hepatitis B

机译:慢性乙型肝炎患者外周血单核细胞和CD3 + CD16 / CD56 +自然杀伤性T细胞中Tim-3的表达

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Hepatitis B virus (HBV) infection is one of the major causes of chronic liver inflammation. Tim-3 acts as a negative regulatory molecule and plays a critical role in immune tolerance. In the current study, we investigated Tim-3 expression on peripheral monocytes and CD3+CD16/CD56+ natural killer like T (NKT-like) cells in chronic hepatitis B (CHB) patients. Peripheral blood mononuclear cells (PBMCs) were isolated from 52 CHB patients and 60 healthy controls. Tim-3+CD14+ cells and Tim-3+CD3+CD16/CD56+ cells were analyzed by flow cytometry. Results showed that expression of Tim-3 was significantly increased on both the monocytes and NKT-like cells in CHB patients than in controls (P=0.002 and P<0.001, respectively). Tim-3 levels on monocytes and NKT-like cells were further upregulated in patients with acute-on-chronic liver failure (ACLF). In addition, we assessed the correlation of Tim-3 expression with levels of alanine aminotransferase (ALT) and tumor necrosis factor alpha (TNF-α). Data revealed that Tim-3 expression on both monocytes and NKT-like cells was positively correlated with level of ALT (r=0.59, P<0.001, and r=0.60, P<0.001, respectively), whereas Tim-3 expression on NKT-like cells was negatively correlated with serum level of TNF-α (r=-0.54, P<0.001) in CHB patients. Our results suggest that Tim-3 may play important roles in the pathogenesis of CHB.
机译:乙型肝炎病毒(HBV)感染是慢性肝炎的主要原因之一。 Tim-3充当负调节分子,在免疫耐受中起关键作用。在当前的研究中,我们调查了慢性乙型肝炎(CHB)患者外周血单核细胞和CD3 + CD16 / CD56 +自然杀伤性T细胞(NKT样)上的Tim-3表达。从52位CHB患者和60位健康对照中分离出外周血单核细胞(PBMC)。通过流式细胞术分析Tim-3 + CD14 +细胞和Tim-3 + CD3 + CD16 / CD56 +细胞。结果显示,与对照组相比,CHB患者单核细胞和NKT样细胞中Tim-3的表达均显着增加(分别为P = 0.002和P <0.001)。慢性肝功能衰竭(ACLF)患者的单核细胞和NKT样细胞上的Tim-3水平进一步上调。此外,我们评估了Tim-3表达与丙氨酸转氨酶(ALT)和肿瘤坏死因子α(TNF-α)水平的相关性。数据显示单核细胞和NKT样细胞上Tim-3的表达与ALT水平呈正相关(r = 0.59,P <0.001,r = 0.60,P <0.001),而NKT上的Tim-3表达慢性乙型肝炎患者血清中TNF-α样细胞与血清TNF-α水平呈负相关(r = -0.54,P <0.001)。我们的结果表明,Tim-3可能在CHB的发病机理中起重要作用。

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