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口服免疫调节蛋白结合多糖PSK后,外周血单核细胞中免疫调节细胞因子基因表达的诱导。

Induction of gene expression for immunomodulating cytokines in peripheral blood mononuclear cells in response to orally administered PSK, an immunomodulating protein-bound polysaccharide.

作者信息

Kato M, Hirose K, Hakozaki M, Ohno M, Saito Y, Izutani R, Noguchi J, Hori Y, Okumoto S, Kuroda D

机构信息

2nd Department of Surgery, Kinki University School of Medicine, Osaka, Japan.

出版信息

Cancer Immunol Immunother. 1995 Mar;40(3):152-6. doi: 10.1007/BF01517346.

DOI:10.1007/BF01517346
PMID:7728773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11037764/
Abstract

The protein-bound polysaccharide extracted from a fungus, PSK, has been used as a biological response modifier in the treatment of cancer patients in Japan for over 16 years. The administration of PSK to tumor-bearing rodents inhibited tumor growth and modulated immune responses. Recently, an in vitro study has revealed that PSK is a strong inducer of cytokine gene expression and production in human peripheral blood mononuclear cells (PBMC). To establish whether PSK has cytokine-inducing activities in vivo, we have orally administered PSK (1 g, the clinical dose) to 12 healthy volunteers and 9 gastric cancer patients who had undergone gastrectomy, and assessed the gene expression for cytokines in PBMC of each subject. As determined by the reverse-transcribed polymerase chain reaction method, the induction of gene expression for both tumor necrosis factor alpha and interleukin-8 (IL-8) was detected in PBMC from 5 of the 12 healthy volunteers (42%) and 4 of the 9 patients (44%). Furthermore, the concentration of serum IL-8 was elevated in 5 healthy volunteers given PSK orally, who had shown induction of IL-8 gene expression, as detected by enzyme-linked immunosorbent assay. These findings indicate that responsiveness of PBMC to PSK, in terms of gene expression and production of cytokines, varies among individuals. Thus, when using PSK to treat cancer patients, it seems advisable to select patients on the basis of their responsiveness to PSK. We speculate that the cytokines induced by PSK might mediate the immunoenhancing action of this agent in vivo.

摘要

从一种真菌中提取的蛋白结合多糖——PSK,在日本作为生物反应调节剂用于癌症患者的治疗已有16年多。给荷瘤啮齿动物施用PSK可抑制肿瘤生长并调节免疫反应。最近,一项体外研究表明,PSK是人类外周血单个核细胞(PBMC)中细胞因子基因表达和产生的强力诱导剂。为确定PSK在体内是否具有细胞因子诱导活性,我们给12名健康志愿者和9名接受过胃切除术的胃癌患者口服PSK(1克,临床剂量),并评估每个受试者PBMC中细胞因子的基因表达。通过逆转录聚合酶链反应法测定,在12名健康志愿者中的5名(42%)和9名患者中的4名(44%)的PBMC中检测到肿瘤坏死因子α和白细胞介素-8(IL-8)基因表达的诱导。此外,通过酶联免疫吸附测定法检测,在口服PSK的5名健康志愿者中,血清IL-8浓度升高,这些志愿者显示出IL-8基因表达的诱导。这些发现表明,PBMC对PSK在细胞因子基因表达和产生方面的反应性因人而异。因此,在使用PSK治疗癌症患者时,根据患者对PSK的反应性来选择患者似乎是明智的。我们推测,PSK诱导的细胞因子可能在体内介导该药物的免疫增强作用。

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Induction of gene expression for immunomodulating cytokines in peripheral blood mononuclear cells in response to orally administered PSK, an immunomodulating protein-bound polysaccharide.口服免疫调节蛋白结合多糖PSK后,外周血单核细胞中免疫调节细胞因子基因表达的诱导。
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Overexpression of mitochondrial manganese superoxide dismutase promotes the survival of tumor cells exposed to interleukin-1, tumor necrosis factor, selected anticancer drugs, and ionizing radiation.线粒体锰超氧化物歧化酶的过表达可促进暴露于白细胞介素-1、肿瘤坏死因子、某些抗癌药物及电离辐射的肿瘤细胞存活。
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