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人类1型和2型辅助性T细胞及其细胞因子的概念。

The concept of type-1 and type-2 helper T cells and their cytokines in humans.

作者信息

Del Prete G

机构信息

Faculty of Medicine, University of Florence, Italy.

出版信息

Int Rev Immunol. 1998;16(3-4):427-55. doi: 10.3109/08830189809043004.

Abstract

In both mice and humans, functionally distinct helper T (Th)-cell subsets, known as Th1 and Th2 cells, are characterized by the patterns of cytokines they produce. These two polarized forms of the specific cellular immune response provide a useful model for explaining not only the different types of protection, but also the pathogenic mechanisms of several immunopathological disorders. The development of polarized Th1 or Th2 responses depends on either environmental factors, including dose of antigen, nature of immunogen and cytokines (IL-12 and interferons or IL-4) at the time of antigen presentation, or other undefined factors in the individual genetic background, mainly at level of the so-called "natural immunity". Th1-dominated responses are potentially effective in eradicating infectious agents, including those hidden within the host cells. When the Th1 response is poorly effective or exhaustively prolonged, it may result in host damage. In contrast, Th2 responses are apparently insufficient to protect against the majority of infectious agents, but can provide some protection against parasites. Th2 cells are able to make unpleasant the life of parasites in the host and tend to limit potentially harmful Th1-mediated responses. Thus, Th2 cells may be regarded as a part of down regulatory (or suppressor) mechanism for exaggerated and/ or inappropriate Th1 responses. The Th1/Th2 paradigm applied to the study of chronic inflammatory disorders or autoimmune diseases allowed to understand that a number of diseases are mediated by Th1 cells, the two clearest examples being multiple sclerosis and thyroid autoimmunity. In other disorders, Th1/Th2 polarization is less prominent, or rather Th2 responses tend to predominate, such as in systemic lupus erythematosus, progressive systemic sclerosis or allergic diseases. It is of note that in experimental models in animals, a number of diseases can be prevented by switching immune responses from Th1 to Th2 or from Th2 to Th1. Moreover, the Th1/Th2 concept suggests that modulation of the relative contribution of Th1- or Th2-type cytokines makes possible to regulate the balance between protection and immunopathology, as well as the development and/or the severity of some immunologic disorders.

摘要

在小鼠和人类中,功能不同的辅助性T(Th)细胞亚群,即Th1细胞和Th2细胞,其特征在于它们产生的细胞因子模式。特异性细胞免疫反应的这两种极化形式不仅为解释不同类型的保护作用,也为解释几种免疫病理疾病的发病机制提供了一个有用的模型。极化的Th1或Th2反应的发展取决于环境因素,包括抗原剂量、免疫原性质以及抗原呈递时的细胞因子(IL-12和干扰素或IL-4),或者个体遗传背景中的其他未明确因素,主要是在所谓的“天然免疫”水平。以Th1为主导的反应在根除包括隐藏在宿主细胞内的病原体方面可能有效。当Th1反应效果不佳或过度延长时,可能会导致宿主损伤。相比之下,Th2反应显然不足以抵御大多数病原体,但可以提供针对寄生虫的一些保护。Th2细胞能够使寄生虫在宿主体内的生存变得不适,并倾向于限制潜在有害的Th1介导的反应。因此,Th2细胞可被视为对过度和/或不适当的Th1反应进行下调(或抑制)机制的一部分。应用于慢性炎症性疾病或自身免疫性疾病研究的Th1/Th2范式使人们认识到,许多疾病是由Th1细胞介导的,最明显的两个例子是多发性硬化症和甲状腺自身免疫。在其他疾病中,Th1/Th2极化不太明显,或者更确切地说,Th2反应往往占主导,如在系统性红斑狼疮、进行性系统性硬化症或过敏性疾病中。值得注意的是,在动物实验模型中,通过将免疫反应从Th1转换为Th2或从Th2转换为Th1,可以预防多种疾病。此外,Th1/Th2概念表明,调节Th1型或Th2型细胞因子的相对贡献有可能调节保护作用与免疫病理学之间的平衡,以及某些免疫疾病的发展和/或严重程度。

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