Boosting interleukin-10 production: therapeutic effects and mechanisms.

Xiaoxia Zhou, Peter Schmidtke, Fred Zepp, Claudius U Meyer
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引用次数: 42

Abstract

More than forty cytokines have been extensively researched on the molecular structure, cell signaling and transduction pathway. With respect to cytokine-regulating therapy in immunological imbalance however, the reported results are conflicting because of the pleiotropic functions and the intricate interactions of the cytokine network. In this review, we outline the observations on interleukin-10 (IL-10) upregulatory therapy. Despite varying opinions on its therapeutic effects for different disorders, IL-10 has been considered a potential anti-inflammatory cytokine. Numerous studies support the view that IL-10 shows a strong suppressive effect on Th1 lymphocytes, antigen presenting cells and the production of inflammatory mediators. It is also noticeable that recent research has revealed the relationship between IL-10 induced antigen specific regulatory CD4+ T cells and antigen specific immune tolerance. This specific regulation was mediated in part through IL-10 secretion, because anti-IL-10 treatment reverted the inhibitory effect of regulatory T cell clones. In different models, these cells were shown to inhibit both Th1 and Th2-type inflammatory responses through the secretion of IL-10. With the presence of IL-10, regulatory T cells may induce peripheral immune tolerance. Exogenous administration, transgenic expression and endogenous stimulative agents of IL-10 have been used for a variety of inflammatory diseases, autoimmune diseases and allograft rejection in patients and experimental models. A therapeutic intervention with drug inducing endogenous IL-10 may be more practical than an exogenous administration of IL-10 with transient effect. Although further investigation on gene regulation of IL-10 is necessary, increasing studies have been reported concerning the attempt to develop the agents, which could promote endogenous IL-10 production for the treatment of immunological disorders and inflammatory diseases. With some unclear mechanisms, these agents have strongly upregulated IL-10 production in vitro or in vivo. Reported IL-10 upregulatory agents have shown promising prospects for remission of autoimmune diseases and inflammatory diseases and have even induced antigen specific immune tolerance. It is interesting that the IL-10 upregulatory effect of several traditional immunosuppressive drugs has been detected, e.g. glucocorticoid, which is considered "not more as an immunosuppressive drug but an immune modulating agent". Approximately twenty IL-10 upregulatory agents as instances are described in the present review. In addition, their therapeutic effects in various diseases are discussed.

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促进白细胞介素-10的产生:治疗效果和机制。
目前已有40多种细胞因子在分子结构、细胞信号转导途径等方面得到了广泛的研究。然而,由于细胞因子网络的多效性和复杂的相互作用,关于细胞因子调节治疗免疫失衡的报道结果相互矛盾。本文就白细胞介素-10 (IL-10)上调治疗的研究进展进行综述。尽管对其治疗不同疾病的效果有不同的看法,但IL-10被认为是一种潜在的抗炎细胞因子。大量研究支持IL-10对Th1淋巴细胞、抗原提呈细胞和炎症介质的产生具有较强的抑制作用。同样值得注意的是,最近的研究揭示了IL-10诱导的抗原特异性调节性CD4+ T细胞与抗原特异性免疫耐受之间的关系。这种特异性调节部分是通过IL-10分泌介导的,因为抗IL-10治疗恢复了调节性T细胞克隆的抑制作用。在不同的模型中,这些细胞通过分泌IL-10来抑制Th1和th2型炎症反应。在IL-10存在的情况下,调节性T细胞可诱导外周免疫耐受。IL-10的外源性给药、转基因表达和内源性刺激剂已被用于多种炎症性疾病、自身免疫性疾病和同种异体移植排斥反应的患者和实验模型。药物诱导内源性IL-10的治疗干预可能比具有瞬时效应的外源性给药IL-10更实用。尽管对IL-10基因调控的进一步研究是必要的,但越来越多的研究报道了开发能够促进内源性IL-10产生的药物以治疗免疫疾病和炎症性疾病的尝试。尽管机制尚不清楚,但这些药物在体内或体外均能强烈上调IL-10的产生。已报道的IL-10上调制剂在自身免疫性疾病和炎症性疾病的缓解中显示出良好的前景,甚至诱导抗原特异性免疫耐受。有趣的是,一些传统的免疫抑制药物已经检测到IL-10的上调作用,例如糖皮质激素,它被认为“与其说是一种免疫抑制药物,不如说是一种免疫调节剂”。在本综述中描述了大约20种IL-10上调剂的实例。此外,还讨论了它们在各种疾病中的治疗作用。
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