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伐替唑啉(ITCL,地诺替韦)的免疫调节活性。

Immunotropic activity of vratizolin (ITCL, Denotivir).

作者信息

Machoń Z, Wieczorek Z, Zimecki M

机构信息

Department of Organic Chemistry, Faculty of Pharmacy, University Medical School, Wrocław, Poland.

出版信息

Pol J Pharmacol. 2001 Jul-Aug;53(4):377-83.

Abstract

The aim of this study was to evaluate immunotropic properties of vratizolin, a known antiviral drug, in several in vitro and in vivo assays in mouse and human models. We demonstrated that vratizolin exerted strong immunosuppressive actions both in the humoral and cellular immune response to SRBC in mice. The compound affected not only the inductive phase of delayed type hypersensitivity (DTH) but also the effector phase of that response. Vratizolin was effective when given intraperitoneally and orally. The inhibitory action of vratizolin was comparable to that of cyclosporin A (CsA), the reference drug. Vratizolin exhibited also suppressory properties with regard to PHA-induced proliferation of human peripheral blood lymphocytes and that effect exceeded the inhibitory action of CsA. We also showed that vratizolin inhibited to some degree LPS-induced cytokine production in human peripheral blood cultures. The activities of TNF-alpha, IL-1 and IL-6 were inhibited on average by 37, 26 and 35%, respectively. This was in contrast to the effects of CsA which strongly inhibited only IL-1 production. Lastly, we demonstrated that vratizolin markedly inhibited growth of several tumor cell lines. In particular, the compound significantly inhibited growth of mouse leukemia L-1210 and human acute lymphoblastoid leukemia CCRF-CEM cell lines. The presented data suggest that the immunosuppressory action of vratizolin, although similar to that of CsA, is mediated by a different mechanism. The properties of vratizolin, described in this report, indicate that the drug should be further investigated for possible immunosuppressory and antitumor application.

摘要

本研究的目的是在小鼠和人类模型的多种体外和体内试验中评估已知抗病毒药物vratizolin的免疫调节特性。我们证明,vratizolin在小鼠对SRBC的体液免疫和细胞免疫反应中均发挥了强大的免疫抑制作用。该化合物不仅影响迟发型超敏反应(DTH)的诱导期,还影响该反应的效应期。vratizolin经腹腔注射和口服给药均有效。vratizolin的抑制作用与参考药物环孢素A(CsA)相当。vratizolin对PHA诱导的人外周血淋巴细胞增殖也具有抑制特性,且该效应超过了CsA的抑制作用。我们还表明,vratizolin在一定程度上抑制人外周血培养物中LPS诱导的细胞因子产生。TNF-α、IL-1和IL-6的活性平均分别被抑制37%、26%和35%。这与CsA的作用相反,CsA仅强烈抑制IL-1的产生。最后,我们证明vratizolin显著抑制几种肿瘤细胞系的生长。特别是,该化合物显著抑制小鼠白血病L-1210和人急性淋巴细胞白血病CCRF-CEM细胞系的生长。所呈现的数据表明,vratizolin的免疫抑制作用虽然与CsA相似,但其作用机制不同。本报告中描述的vratizolin的特性表明,该药物应进一步研究其可能的免疫抑制和抗肿瘤应用。

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