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Multi-Step Pathogenesis and Induction of Local Immune Response by Systemic Candida Albicans Infection in an Intravenous Challenge Mouse Model

机译:多步骤发病机制和静脉注射攻击小鼠模型中的系统性白色念珠菌感染诱导局部免疫反应。

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摘要

Different murine species differ in their susceptibility to systemic infection with Candida albicans, giving rise to varied host immune responses, and this is compounded by variations in virulence of the different yeast strains used. Hence, this study was aimed at elucidating the pathogenesis of a clinical C. albicans isolate (HVS6360) in a murine intravenous challenge model by examining the different parameters which included the counts of red blood cells and associated components as well as the organ-specific expression profiles of cytokines and chemokines. Kidneys and brains of infected mice have higher fungal recovery rates as compared to other organs and there were extensive yeast infiltration with moderate to severe inflammation seen in kidney and brain tissues. Red blood cells (RBCs) and haemoglobin (Hb) counts were reduced throughout the infection period. Pattern recognition receptors (PRRs), chemokines and cytokine transcription profiles were varied among the different organs (kidney, spleen and brain) over 72 h post infections. Transcription of most of the PRRs, cytokines and chemokines were suppressed at 72 h post infection in spleen while continuous expression of PRRs, cytokines and chemokines genes were seen in brain and kidney. Reduction in red blood cells and haemoglobin counts might be associated with the action of extracellular haemolysin enzyme and haeme oxygenase of C. albicans in conjunction with iron scavenging for the fungal growth. Renal cells responsible for erythropoietin production may be injured by the infection and hence the combined effect of haemolysis plus lack of erythropoietin-induced RBC replenishment leads to aggravated reduction in RBC numbers. The varied local host immune profiles among target organs during systemic C. albicans infection could be of importance for future work in designing targeted immunotherapy through immunomodulatory approaches.
机译:不同的鼠类物种对白色念珠菌的全身感染的敏感性不同,从而导致宿主免疫反应不同,并且所用不同酵母菌株的毒力变化也加剧了这种情况。因此,本研究旨在通过检查包括红细胞计数及相关成分以及器官特异性表达在内的不同参数,阐明鼠类静脉攻击模型中临床白色念珠菌分离株(HVS6360)的发病机理。细胞因子和趋化因子的概况。与其他器官相比,受感染小鼠的肾脏和大脑的真菌恢复率更高,并且在肾脏和脑组织中可见大量酵母浸润,并伴有中度至重度炎症。在整个感染期间,红细胞(RBCs)和血红蛋白(Hb)计数均降低。感染后72小时内,不同器官(肾脏,脾脏和大脑)的模式识别受体(PRRs),趋化因子和细胞因子转录谱发生变化。感染后72小时,脾脏中大多数PRR,细胞因子和趋化因子的转录被抑制,而在脑和肾脏中观察到PRR,细胞因子和趋化因子基因的连续表达。红细胞和血红蛋白数量的减少可能与白色念珠菌的细胞外溶血酶和血红素加氧酶的作用以及铁清除真菌的生长有关。感染可能会损害负责促红细胞生成素产生的肾细胞,因此溶血加缺乏促红细胞生成素诱导的RBC补充的综合作用会导致RBC数量的严重减少。在全身性白色念珠菌感染过程中,靶器官间不同的局部宿主免疫谱对于通过免疫调节方法设计靶向免疫疗法的未来工作可能具有重要意义。

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