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“固有”宿主反应对受感染的尿路既有保护作用,也有损害作用。

The 'innate' host response protects and damages the infected urinary tract.

作者信息

Svanborg C, Bergsten G, Fischer H, Frendéus B, Godaly G, Gustafsson E, Hang L, Hedlund M, Karpman D, Lundstedt A C, Samuelsson M, Samuelsson P, Svensson M, Wullt B

出版信息

Ann Med. 2001 Dec;33(9):563-70. doi: 10.3109/07853890109002101.

Abstract

Symptoms of infection and tissue pathology are caused by the host response; not by the microbe per se. The same response is also critical for the defence and is needed to clear infection. It is therefore essential to understand how the host response is activated and to identify the critical effector mechanisms of the defence. We have studied these issues in the urinary tract infection (UTI) model. The symptoms of UTI and the host defence both rely on the so-called 'innate' immune system, making this one of the best characterized human disease models of 'innate immunity. We discuss the critical molecular events that determine whether the host response will be activated by P-fimbriated uropathogenic Escherichia coli as well as factors determining whether the patient develops acute pyelonephritis or asymptomatic bacteriuria. We will describe the glycoconjugate receptors used by the P-fimbriated bacteria adhering to host tissues, the recruitment of TLR4 co-receptors and the signalling pathways that allow progression to symptomatic disease, and discuss how these mechanisms are altered in asymptomatic carriers, presenting the possible genetic basis for unresponsiveness. We have shown that neutrophils are the critical effectors of the host defence and that neutrophil dysfunctions lead to acute pyelonephritis and renal scarring. Here we discuss the mechanisms of neutrophil-mediated, chemokine receptor (CXCR1)-dependent clearance, and the defect in interleukin-8 receptor homolog knock-out (IL-8Rh KO) mice and describe the data linking low CXCR1 expression to recurrent pyelonephritis in man, as well as the information on the genetic basis for low CXCR1 expression in affected patients. Finally, the mechanisms of renal scarring in IL8Rh KO mice will be discussed in relation to human disease. Our studies hold the promise to provide a molecular and genetic explanation for disease susceptibility in some patients with UTI and to offer more precise tools for the diagnosis and therapy of these infections.

摘要

感染症状和组织病理学是由宿主反应引起的,而非微生物本身。同样的反应对防御也至关重要,是清除感染所必需的。因此,了解宿主反应如何被激活以及识别防御的关键效应机制至关重要。我们在尿路感染(UTI)模型中研究了这些问题。UTI的症状和宿主防御都依赖于所谓的“固有”免疫系统,这使其成为“固有免疫”特征最明显的人类疾病模型之一。我们讨论了决定宿主反应是否会被产P菌毛的尿路致病性大肠杆菌激活的关键分子事件,以及决定患者是发展为急性肾盂肾炎还是无症状菌尿的因素。我们将描述产P菌毛细菌粘附于宿主组织所使用的糖缀合物受体、Toll样受体4(TLR4)共受体的募集以及导致出现症状性疾病的信号通路,并讨论这些机制在无症状携带者中是如何改变的,提出无反应性的可能遗传基础。我们已经表明,中性粒细胞是宿主防御的关键效应细胞,中性粒细胞功能障碍会导致急性肾盂肾炎和肾瘢痕形成。在这里,我们讨论中性粒细胞介导的、趋化因子受体(CXCR1)依赖性清除机制,以及白细胞介素-8受体同源物敲除(IL-8Rh KO)小鼠中的缺陷,并描述将低CXCR1表达与人类复发性肾盂肾炎联系起来的数据,以及受影响患者中CXCR1低表达的遗传基础信息。最后,将结合人类疾病讨论IL-8Rh KO小鼠肾瘢痕形成的机制。我们的研究有望为一些UTI患者的疾病易感性提供分子和遗传学解释,并为这些感染的诊断和治疗提供更精确的工具。

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