Activation of tumor necrosis factor-α system in chronic hepatitis C virus infection

被引:167
作者
Nelson, DR
Lim, HL
Marousis, CG
Fang, JWS
Davis, GL
Shen, LP
Urdea, MS
Kolberg, JA
Lau, JYN
机构
[1] Univ Florida, Dept Med, Sect Hepatobiliary Dis, Div Gastroenterol Hepatol & Nutr, Gainesville, FL USA
[2] Chiron Corp, Nucl Acids Syst, Emeryville, CA 94608 USA
基金
美国国家卫生研究院;
关键词
hepatitis C virus; hepatitis C; tumor necrosis factor-alpha; receptors; peripheral blood mononuclear cells; cytokines; pathogenesis;
D O I
10.1023/A:1018804426724
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Tumor necrosis factor-alpha (TNF-alpha) plays a central role in the host's immunomodulatory response to infective agents. To evaluate the TNF-alpha system in patients with chronic hepatitis C virus (HCV) infection, plasma, serum, and peripheral blood mononuclear cells (PBMC) were prospectively collected from 53 patients and 33 healthy control subjects. Circulating TNF-alpha and TNF receptors were assayed by their respective enzyme immunoassays. In addition, TNF-alpha mRNA was quantitated in PBMC using a branched DNA assay, and production of TNF-alpha by PBMC with and without lipopolysaccharide was also assessed. Patients with chronic HCV infection had a higher level of circulating TNF-alpha compared to healthy control subjects (9.62 +/- 6.01 vs 3.66 +/- 1.23 pg/ml, P < 0.001). They also had higher circulating levels of TNF receptors compared to control (CD120a: 3323 +/- 1267, pg/ml, N = 49 vs 1855 +/- 422 pg/ml, N = 33, P < 0.001; CD120b: 1290 +/- 650 pg/ml, N = 51, vs 863 +/- 207 pg/ml, N = 33, P < 0.001). Plasma TNF-alpha level correlated with circulating CD120a (r = 0.52, N = 49, P < 0.001) and weakly with CD120b (r = 0.32, N = 51, P = 0.02). Plasma TNF-alpha also correlated with markers of hepatocellular injury, including ALT (r = 0.34, N = 53, P = 0.01) and alpha-GST (r = 0.31, N = 43, P = 0.042), but not with serum HCV RNA levels. There was no difference in the TNF-alpha mRNA levels in PBMC between patients with chronic HCV infection (1.4 +/- 1.9 units/10(6) cells: N = 8) and healthy control subjects (2.1 +/- 1.4 units/10(6) cells, N = 8, P = NS). There was also no difference in the spontaneous production of TNF-alpha by PBMC (1 x 10(6) cells/ml) between patients with chronic HCV infection (14.2 +/- 36.5 pg/ml, N = 11) and healthy subjects (11.9 +/- 14.0 pg/ml, N = 14, P = NS). However, patients with chronic HCV infection produced more TNF-alpha upon stimulation with lipopolysaccharide compared to healthy control subjects (1278 +/- 693 pg/ml, N = 11, vs 629 +/- 689 pg/ml, N = 14, P < 0.05). These data indicate that the TNF-alpha system is activated in patients with chronic HCV infection.
引用
收藏
页码:2487 / 2494
页数:8
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