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恒河猴实验性吸入性炭疽的病理学

Pathology of experimental inhalation anthrax in the rhesus monkey.

作者信息

Fritz D L, Jaax N K, Lawrence W B, Davis K J, Pitt M L, Ezzell J W, Friedlander A M

机构信息

Pathology Division, U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick, Frederick, Maryland, USA.

出版信息

Lab Invest. 1995 Nov;73(5):691-702.

PMID:7474943
Abstract

BACKGROUND

The inhalation form of anthrax, although rare, is nearly always fatal because of the rapid progression of the disease with little host response until the terminal stages of the disease. The Gulf War heightened the concern that anthrax could be used as a biologic weapon. Past studies modeling pathologic changes in human inhalation anthrax have used the rhesus monkey.

EXPERIMENTAL DESIGN

We studied pathologic changes in the rhesus monkey model of inhalation anthrax. Gross examination as well as light and electron microscopy were used to define pathologic alterations. Immunolabeling techniques were used to identify the anthrax bacillus by light and electron microscopy.

RESULTS

Gross changes included hemorrhage in mesenteric (54%) and tracheobronchial (46%) lymph nodes, meninges (38%), lungs (31%), and small intestinal serosa (31%). Histopathologic changes included suppurative meningitis (77%); hemorrhages in the meninges (54%), neuropil (31%), and pulmonary alveoli (31%); and pneumonia (15%). Spleens and various lymph nodes from all monkeys had one or more of the following changes: hemorrhage, acute inflammation, extracellular bacilli, lymphocytic depletion, and histiocytosis. Spleens of two monkeys were devoid of extracellular bacilli, but degraded intrahistiocytic bacilli reacted with Ab to Bacillus anthracis cell wall polysaccharide.

CONCLUSIONS

In our study, compared with previous reports, meningitis and mesenteric lymph node hemorrhages were more common, whereas mediastinal and tracheobronchial lymph node hemorrhages were less common. Immunostaining highlighted intracellular bacilli that would have been otherwise missed by light microscopic examination.

摘要

背景

吸入性炭疽虽然罕见,但几乎总是致命的,因为该疾病进展迅速,在疾病晚期之前宿主几乎没有反应。海湾战争加剧了人们对炭疽可能被用作生物武器的担忧。过去模拟人类吸入性炭疽病理变化的研究使用的是恒河猴。

实验设计

我们研究了恒河猴吸入性炭疽模型的病理变化。采用大体检查以及光镜和电镜来确定病理改变。免疫标记技术用于通过光镜和电镜鉴定炭疽杆菌。

结果

大体变化包括肠系膜淋巴结(54%)、气管支气管淋巴结(46%)、脑膜(38%)、肺(31%)和小肠浆膜(31%)出血。组织病理学变化包括化脓性脑膜炎(77%);脑膜(54%)、神经纤维(31%)和肺泡(31%)出血;以及肺炎(15%)。所有猴子的脾脏和各种淋巴结有以下一种或多种变化:出血、急性炎症、细胞外杆菌、淋巴细胞耗竭和组织细胞增多。两只猴子的脾脏没有细胞外杆菌,但组织细胞内降解的杆菌与抗炭疽杆菌细胞壁多糖抗体发生反应。

结论

在我们的研究中,与之前的报告相比,脑膜炎和肠系膜淋巴结出血更为常见,而纵隔和气管支气管淋巴结出血则较少见。免疫染色突出显示了光镜检查可能会遗漏的细胞内杆菌。

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