Long-term follow-up of chronic hepatitis C patients treated with oral lactoferrin for 12 months

被引:52
作者
Ishii, K
Takamura, N
Shinohara, M
Wakui, N
Shin, H
Sumino, Y
Ohmoto, Y
Teraguchi, S
Yamauchi, K
机构
[1] Toho Univ, Sch Med, Dept Internal Med 2, Ota Ku, Tokyo 143, Japan
[2] Otsuka Pharmaceut Co Ltd, Inst New Drug Res 1, Tokushima 77101, Japan
[3] Morinaga Milk Ind Ltd, Nutrit Sci Lab, Kanagawa, Japan
关键词
lactoferrin; chronic hepatitis C; IL-18; IL-10; Th1; Th2; TOLL-LIKE RECEPTOR-2; T-CELLS; VIRUS VIREMIA; RIBAVIRIN; COMBINATION; INTERFERON; EXPRESSION; RESISTANT; RESPONSES; GENOTYPE;
D O I
10.1016/S1386-6346(02)00279-6
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Bovine lactoferrin (bLF) has been shown to prevent the infection of cultured hepatocytes by hepatitis C virus (HCV). The present study attempted to clarify the effects of long-term administration of bLF on serum parameters, including immunomodulatory cytokines, in patients with chronic hepatitis C (CHC). Methods: Sixty-three CHC patients were randomly assigned into 2 groups. At an oral dose of 600 mg/day, bLF was administered for 12 months to 36 patients (bLF group), while no bLF was given to the remaining 27 patients (control group. Serum levels of alanine aminotransferase, HCV-RNA, IL-10, and IL-18 were evaluated, as well as CD4-positive T cell subsets in the peripheral blood. Results: The serum IL-18 level was increased by bLF administration, but not in the control group. After 3 months of bLF treatment, it was significantly higher than before bLF administration, but it decreased gradually thereafter. The percentage of interferon (IFN)-gamma+ and IL-4- (Th1) cells in the peripheral blood increased along with the serum IL-18 level, although the change was not statistically significant. The other parameters did not change significantly during the study period in both groups. Conclusions: These results suggest that oral administration of bLF to CHC patients for up to 3 months can produce a Th1-cytokine dominant environment in the peripheral blood that favors the eradication of HCV by IFN therapy. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:226 / 233
页数:8
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