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使小鼠对曼氏血吸虫卵抗原产生耐受性会导致1型细胞因子反应增强、2型细胞因子反应减弱以及急性感染时死亡率增加。

Tolerization of mice to Schistosoma mansoni egg antigens causes elevated type 1 and diminished type 2 cytokine responses and increased mortality in acute infection.

作者信息

Fallon P G, Dunne D W

机构信息

Department of Pathology, University of Cambridge, United Kingdom.

出版信息

J Immunol. 1999 Apr 1;162(7):4122-32.

Abstract

The granuloma that surrounds the Schistosoma mansoni egg is the cause of pathology in murine schistosomiasis, and its formation is driven by egg Ag-stimulated type 1 and type 2 cytokines. To determine the role of egg-driven immune responses during schistosome infection we rendered CBA/Ca mice unresponsive to schistosome eggs by combined cyclophosphamide treatment and thymectomy. In the early acute stages of schistosome infection, egg-tolerized mice suffered high mortalities. Granuloma size and deposition of collagen in the liver were significantly reduced in egg-tolerized mice. Similarly, limited granuloma responses were detected in the intestines of these mice, and this was associated with a >90% reduction in egg excretion. Histologically, egg-tolerized mice had exacerbated hepatocyte damage, with extensive microvesicular steatosis. Elevated plasma transaminase levels confirmed the damage to hepatocytes. Infected egg-tolerized mice had impaired proliferation responses to egg Ag but intact responses to worm Ag. Tolerized mice had diminished Ab responses to egg Ag and had a type 1 cytokine isotype pattern to worm Ag, with elevated IgG2a and diminished IgG1 and IgE. Egg-tolerized mice failed to down-regulate type 1 cytokines that are normally elicited during early schistosome infection. Hepatic granuloma cells from egg-tolerized mice were also type 1 cytokine dominated, with elevated frequencies of Tc1/Th1 and reduced Tc2/Th2 cells. This study demonstrates that mice tolerized to schistosome eggs have elevated type 1 cytokine responses with diminished type 2 responses and reduced anti-egg Ab during schistosome infection, and these effects are detrimental to the host.

摘要

围绕曼氏血吸虫虫卵的肉芽肿是小鼠血吸虫病病理变化的原因,其形成由虫卵抗原刺激的1型和2型细胞因子驱动。为了确定血吸虫感染期间虫卵驱动的免疫反应的作用,我们通过联合环磷酰胺治疗和胸腺切除术使CBA/Ca小鼠对血吸虫虫卵无反应。在血吸虫感染的早期急性期,对虫卵耐受的小鼠死亡率很高。对虫卵耐受的小鼠肝脏中的肉芽肿大小和胶原蛋白沉积显著减少。同样,在这些小鼠的肠道中检测到有限的肉芽肿反应,这与虫卵排泄减少>90%相关。组织学上,对虫卵耐受的小鼠肝细胞损伤加剧,伴有广泛的微泡性脂肪变性。血浆转氨酶水平升高证实了肝细胞的损伤。感染了虫卵的耐受小鼠对虫卵抗原的增殖反应受损,但对虫体抗原的反应完整。耐受小鼠对虫卵抗原的抗体反应减弱,对虫体抗原具有1型细胞因子同型模式,IgG2a升高,IgG1和IgE降低。对虫卵耐受的小鼠未能下调早期血吸虫感染期间通常引发的1型细胞因子。对虫卵耐受的小鼠的肝肉芽肿细胞也以1型细胞因子为主,Tc1/Th1频率升高,Tc2/Th2细胞减少。这项研究表明,对血吸虫虫卵耐受的小鼠在血吸虫感染期间1型细胞因子反应升高,2型反应减弱,抗虫卵抗体减少,这些影响对宿主有害。

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