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肠道黏膜免疫的兔模型:I. 病毒感染回肠袢的建立

Rabbit model for mucosal immunity in the bowel: I. Establishment of virus-infected ileal loops.

作者信息

Holmes M J, Ramsay A J

机构信息

Department of Microbiology, University of Otago, Dunedin, New Zealand.

出版信息

J Med Virol. 1988 Jul;25(3):271-80. doi: 10.1002/jmv.1890250304.

Abstract

An animal model was designed for use in studies of initial cellular immune responses to virus infection of the intestinal mucosa. The animal chosen was the New Zealand White rabbit and the mucosal site the subterminal ileum, isolated in a Thirty-Vella loop. The antigen used was parainfluenzavirus type 3, which would normally be destroyed by bile salts if ingested. Loops approximately 20 cm in length, each containing at least one Peyer's patch, were exteriorised through left paramedian stomata. Atrophic changes began to appear in the loops by 7 days, but no observable diminution in their associated lymphoid tissues was evident. The genesis of parainfluenzavirus type 3 infection in the loops was monitored by assay of sequential loop washings for infectious virus and in fluorescent antibody studies of cells from infected loop epithelia. Infectious virus was recovered for up to 13 days after inoculation and specific intracytoplasmic immunofluorescence was detected in loop epithelial cells. There was little serological evidence of systemic spread of the virus. A localised cellular immune response against parainfluenzavirus type 3 was mounted in the lymphoid tissues associated with the infected loops by day 14, but was not detected in systemic lymphoid tissues. No reactivity was detected in rabbits given inactivated virus via their loops or in those receiving infectious virus intravenously. This model appears to be capable of generating mucosal cellular responses to infection and may therefore be suitable for further studies in this field.

摘要

设计了一种动物模型,用于研究肠道黏膜对病毒感染的初始细胞免疫反应。选用的动物是新西兰白兔,黏膜部位是回肠末端下部分,通过三十维拉氏袢进行分离。使用的抗原是3型副流感病毒,如果摄入,该病毒通常会被胆汁盐破坏。长度约为20厘米的肠袢,每个都包含至少一个派尔集合淋巴结,通过左旁正中切口引出。到第7天时,肠袢开始出现萎缩变化,但相关淋巴组织未观察到明显减少。通过对连续的肠袢冲洗液进行传染性病毒检测以及对感染肠袢上皮细胞进行荧光抗体研究,监测肠袢中3型副流感病毒感染的发生情况。接种后长达13天可回收传染性病毒,并且在肠袢上皮细胞中检测到特异性胞浆免疫荧光。几乎没有血清学证据表明病毒发生全身扩散。到第14天时,在与感染肠袢相关的淋巴组织中对3型副流感病毒产生了局部细胞免疫反应,但在全身淋巴组织中未检测到。通过肠袢给予灭活病毒的兔子或静脉注射传染性病毒的兔子均未检测到反应性。该模型似乎能够产生针对感染的黏膜细胞反应,因此可能适用于该领域的进一步研究。

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