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Lymphocyte-based model systems for allergy research: A historic overview

机译:基于淋巴细胞的过敏研究模型系统:历史概述

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During the last decades, a multitude of studies applying distinct in vitro and in vivo model systems have contributed greatly to our better understanding of the initiation and regulation of inflammatory processes leading to allergic diseases. Over the years, it has become evident that among lymphocytes, not only IgE-producing B cells and allergy-orchestrating CD4+ helper cells but also cytotoxic CD8+ T cells, γδ-T cells and innate lymphoid cells, as well as regulatory lymphocytes, might critically shape the immune response towards usually innocuous allergens. In this review, we provide a historic overview of pioneering work leading to the establishment of important lymphocyte-based model systems for allergy research. Moreover, we contrast the original findings with our currently more refined knowledge to appreciate the actual validity of the respective models and to reassess the conclusions obtained from them. Conflicting studies and interpretations are identified and discussed. The tables are intended to provide an easy overview of the field not only for scientists newly entering the field but also for the broader readership interested in updating their knowledge. Along those lines, herein we discuss in vitro and in vivo approaches to the investigation of lymphocyte effector cell activation, polarization and regulation, and describe depletion and adoptive transfer models along with gene knockout and transgenic (tg) methodologies. In addition, novel attempts to establish humanized T cell antigen receptor tg mouse models for allergy research are described and discussed.
机译:在过去的几十年中,应用不同的体外和体内模型系统的大量研究为我们更好地理解引发过敏性疾病的炎症过程的启动和调控做出了巨大贡献。多年来,很明显,在淋巴细胞中,不仅产生IgE的B细胞和过敏性CD4 +辅助细胞,而且细胞毒性CD8 + T细胞,γδ-T细胞和先天性淋巴样细胞以及调节性淋巴细胞都可能至关重要。形成对通常无害的过敏原的免疫反应。在这篇评论中,我们提供了有关开拓性工作的历史性概述,这些工作导致建立了基于淋巴细胞的重要变态反应研究模型系统。此外,我们将原始发现与我们目前更完善的知识进行了对比,以欣赏各个模型的实际有效性并重新评估从中得出的结论。确定并讨论了相互矛盾的研究和解释。这些表格不仅为刚进入该领域的科学家,而且为有兴趣更新其知识的广大读者提供了对该领域的轻松概述。沿着这些思路,我们在此讨论了研究淋巴细胞效应细胞激活,极化和调节的体外和体内方法,并描述了基因敲除和转基因(tg)方法的耗竭和过继转移模型。此外,描述和讨论了建立人源化T细胞抗原受体tg小鼠模型进行变态反应研究的新尝试。

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