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Editorial [Hot Topic: Recent Progresses in 'Atypical' Applications of Cytokine and Anti-Cytokine (Executive Editor: Atsushi Oda)]

机译:社论[热门话题:细胞因子和抗细胞因子在“非典型”应用中的最新进展(执行编辑:小田淳)

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Recently several issues of Current Pharmaceutical Design have been dedicated to cytokines and their clinical applications. The topics on conventional and novel aspects in the field have been extensively covered by the reviews in them. As such, my purpose is to bring up-to-date information on somewhat "atypical" cytokine-related therapies. In this issue of Current Pharmaceutical Design, I invited six experts and their associates to present comprehensive reviews on these emerging topics.nnI would like to briefly introduce these exciting reviews. Feller and Lewitzky summarize the biology of adapter proteins, with emphasis on Crk and grb2. Both Crk and grb2 are classical adapters of protein-to-protein interaction without known catalytic domains. Alongwith other adapters, CrkL (Crk-like) and Nck, they are involved in signaling, triggered by ligasion of numerous cytokine/growth factor receptors. With 384 references, the readers will find this review exceptionally useful, to keep up with the rapid progresses in our understanding of these adapters and their ligands. Moreover, they also present the potential development of pharmacological reagents, which may modify the protein-to-protein interactions. It is seemingly a challenge, given that these adapters are keys players in so many different signaling pathways. On the other hand, once developed, such reagents may have very widespread applications in diverse clinical settings. Next, Ariga summarizes the development of gene therapy for treatment of primary immunodeficiency [2]. Recombinant cytokines are quite expensive and have only short half life time. Obviously, a gene therapy may be a choice for continual administration of cytokines. Among numerous trials of the gene therapies, those for treatment of immunodeficiency have been most successful. However, as he presents, there appears to be serious inherent problems in the therapy.nnRecombinant G-CSF has been extensively used to facilitate recovery of peripheral neutrophil counts following chemotherapy and/or bone marrow transplantation. It is also used for mobilization of multipotent immature hematopoietic cells for transplantation. Somewhat atypical, but the most promising utilization of the cytokine is for the treatment of ischemic heart diseases. This review by Komuro's group [3] is a sequel to a review, recently published in Current Pharmaceutical Design [4]. The readers may notice numerous and sometimes-conflicting evidences presented in the fields. Their well-balanced review gives pretty nice pictures of somewhat chaotic situations.nnProtection of cells from apoptosis is mediated by cytokines. Surprisingly, cilostazol, a well-established, anti-platelet reagent [5], may have a "cytokine-like" function and rescue neuronal cells in ischemic regions. This interesting application of cilostazol is reviewed by Hong's group, who has actually published most of works on this unique aspect of the anti-platelet reagent [6].nnFinally, I have also asked two expert groups to summarize two naturally occurring cytokine-like substances. Yatomi, who has established that platelets are a major source of circulating sphingosine 1-phophate, concisely summarizing the diverse functions of the bioactive-lipid [7]. Agonists and antagonists of its receptors are being developed and potential application of these in clinical setting is also described in depth. Kuroki's group calls attention to novel and evolving fields of lung surfactant proteins [8]. The cytokine-like function of these proteins, which regulates the innate immunity, is well presented. They are not just surfactants, but actually are key players in inflammation and immunity in lung tissues.nnI hope that the readers will really enjoy these reviews on the emerging field of cytokine and anti-cytokine therapies, just as I do.
机译:最近,《当前药物设计》的若干期致力于细胞因子及其临床应用。有关本领域中常规和新颖方面的主题已被其中的评论广泛涵盖。因此,我的目的是提供有关“非典型”细胞因子相关疗法的最新信息。在本期《当前药物设计》中,我邀请了六位专家及其同事对这些新兴主题进行了全面的评论。nnI希望简要介绍这些令人兴奋的评论。 Feller和Lewitzky总结了衔接蛋白的生物学特性,重点是Crk和grb2。 Crk和grb2都是没有已知催化结构域的蛋白质与蛋白质相互作用的经典衔接子。与其他衔接子CrkL(类Crk)和Nck一起,它们参与信号传递,是由众多细胞因子/生长因子受体的脂化触发的。有了384篇参考文献,读者会发现本评论特别有用,以适应我们对这些衔接子及其配体的快速了解。此外,他们还提出了药理学试剂的潜在发展,它可能会改变蛋白质与蛋白质之间的相互作用。鉴于这些适配器是许多不同信号通路中的关键角色,因此这似乎是一个挑战。另一方面,一旦开发,这种试剂在各种临床环境中可能具有非常广泛的应用。接下来,Ariga总结了用于治疗原发性免疫缺陷的基因疗法的发展[2]。重组细胞因子非常昂贵,并且半衰期很短。显然,基因疗法可能是连续施用细胞因子的一种选择。在众多的基因疗法试验中,用于治疗免疫缺陷的疗法最为成功。然而,正如他介绍的那样,该疗法似乎存在着严重的内在问题。重组G-CSF已被广泛用于促进化疗和/或骨髓移植后外周嗜中性粒细胞计数的恢复。它还可用于动员多能的未成熟造血细胞进行移植。细胞因子某种程度上是非典型的,但最有希望的用途是用于治疗缺血性心脏病。 Komuro小组的这篇评论[3]是最近发表在Current Pharmaceutical Design [4]上的一篇评论的续集。读者可能会注意到在这些领域中出现的许多有时是矛盾的证据。他们的平衡评论很好地描绘了一些混乱情况。nn细胞凋亡对细胞的保护是由细胞因子介导的。令人惊讶的是,西洛他唑(一种成熟的抗血小板药[5])可能具有“类细胞因子”的功能,可以在缺血区域拯救神经元细胞。 Hong的研究小组对西洛他唑的这一有趣应用进行了审查,Hong的研究小组实际上已经发表了有关抗血小板试剂这一独特方面的大部分著作[6]。最后,我还请两个专家小组总结了两种天然存在的细胞因子样物质。 Yatomi已确定血小板是循环鞘氨醇1-磷酸的主要来源,简明地总结了生物活性脂质的多种功能[7]。其受体的激动剂和拮抗剂正在开发中,并且还将深入描述其在临床环境中的潜在应用。黑木的研究组呼吁关注肺表面活性剂蛋白的新领域和不断发展的领域[8]。这些蛋白质调节先天免疫的细胞因子样功能已被很好地展现出来。它们不仅是表面活性剂,而且实际上是肺组织炎症和免疫力的关键参与者。我希望读者像我一样,能在新兴的细胞因子和抗细胞因子疗法领域真正受益于这些评论。

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