病原体相关分子模式,模式识别受体和儿科败血症

L. Doughty
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引用次数: 7

摘要

在过去的二十年中,由于更好的支持性护理,儿童感染性休克的死亡率有所改善,但仍然高得令人无法接受。脓毒性休克早期过度的炎症反应与不良预后相关。早期炎症反应强度的调控尚不清楚。对病原体的炎症反应的最早方面是先天免疫反应,这对病原体的遏制很重要。先天免疫系统的元素以抗原特异性的方式激活适应性免疫系统,从而导致病原体特异性保护和持久的免疫记忆,以防止随后的感染。模式识别受体(PRRs)是多种先天免疫细胞上的进化保守受体,能够对病原体中称为病原体相关分子模式(pathogen associated molecular patterns, PAMPs)的高度保守成分做出反应。已经确定了许多PRRs,它们存在于细胞表面和细胞质中。这些受体分为几类,toll样受体在细胞表面或内体质膜上表达,C型凝集素受体和只存在于细胞表面的清道夫受体。其他PRRs存在于细胞质中,包括nod样受体,它们可以聚集形成炎症小体和RIG1样受体。病原微生物种类繁多,但在细胞壁等结构成分中有一些重复的共同模式。PRRs可以对由蛋白质、脂质、碳水化合物、DNA和RNA组成的PAMPs做出反应。许多种类的病原微生物,如革兰氏阴性菌、革兰氏阳性菌、病毒、真菌和原生动物,已经发现了许多PAMPs。PRRs和PAMPs之间的相互作用构成了对外来物质的最早免疫反应,对病原体控制和扩大免疫反应的全部功能至关重要。与成人相比,婴儿和儿童的免疫系统存在发育差异。先天免疫系统比适应性免疫反应成熟得早得多,因此婴幼儿可能更依赖先天免疫系统。因此,重要的是要充分了解先天免疫反应的关键因素,包括许多类别的PRRs及其同源PAMPs。由于这些相互作用在免疫反应中非常早期,因此它们是治疗干预的特别相关目标。下面是对主要类型的PRRs、它们的表达、配体、信号通路以及激活它们的主要类型PAMPs的讨论。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pathogen Associated Molecular Patterns, Pattern Recognition Receptorsand Pediatric Sepsis
The mortality of septic shock in the pediatric population has improved over the last 2 decades with better supportive care however it still remains unacceptably high. Exaggerated inflammatory responses early in septic shock have been associated with poor outcomes. Regulation of the magnitude of the early inflammatory response is not well understood. The earliest aspect of the inflammatory response to pathogens is the innate immune response which is important to pathogen containment. Elements of the innate immune system activate the adaptive immune system in an antigen-specific way which leads to pathogen-specific protection and lasting immunologic memory to prevent subsequent infection. Pattern recognition receptors (PRRs) are evolutionarily conserved receptors on multiple types of innate immune cells and are capable of responding to highly conserved components of pathogens called pathogen associated molecular patterns (PAMPs). Numerous PRRs have been defined and are present on the cell surface as well as in the cytosol. These receptors fall into several classes called Toll-like receptors which are expressed on the cell surface or on the endosomal plasma membrane, C type lectin receptors and scavenger receptors which are only present on the cell surface. Other PRRs are present in the cytosol and including NOD-like receptors which can aggregate to form inflammasomes and RIG1 like receptors. Pathogenic microorganisms are extremely diverse however there are some common patterns repeated in components of structures such as the cell wall. PRRs can respond to PAMPs comprised of proteins, lipids, and carbohydrates, DNA and RNA. Numerous PAMPs have been described for many classes of pathogenic microorganisms such as Gram negative bacteria, Gram positive bacteria, viruses, fungi, and protozoa. The interactions between PRRs and PAMPs comprise the earliest immune responses to foreign substances and are critical for pathogen containment and amplification of the full repertoire of the immune response. There are developmental differences in the immune systems of infants and children compared to adults. The innate immune system matures much earlier than the adaptive immune response and as a result infants and young children may be more reliant on their innate immune system. For this reason it important to fully understand the key elements of the innate immune response including the many categories of PRRs and their cognate PAMPs. As these interactions are very early in the immune response, they are particularly relevant targets for therapeutic intervention. Below is a discussion of the major classes of PRRs, their expression, ligands, and signaling pathways as well as the major classes of PAMPs that activate them.
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