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在小鼠模型中针对反刍动物衣原体菌株的免疫反应差异。

Differences in the immune response against ruminant chlamydial strains in a murine model.

作者信息

Buendía A J, Sánchez J, Del Rio L, Garcés B, Gallego M C, Caro M R, Bernabé A, Salinas J

机构信息

Departamento de Patología Animal (Microbiología e Immunología), Facultad de Veterinaria, Universidad de Murcia, Spain.

出版信息

Vet Res. 1999 Sep-Oct;30(5):495-507.

Abstract

CBA/J mice were used in the present study to establish differences between the immune response to three chlamydial strains: AB7 (Chlamydia psittaci wild-type strain), 1B (C. psittaci vaccinal strain) and iB1 (C. pecorum). The evolution of chlamydial infection was evaluated in each strain by studying the clinical signs, the number of bacteria isolated from the spleen and the pathology of the liver. Three aspects of the immune response were then studied: the characterization of the infiltrate of leukocytes in the liver, the percentages of T- and B-cells, macrophages and neutrophils in the spleen, and the presence of cytokines in the serum. Infection followed a different course in the C. psittaci-infected mice; 1B-infected mice showed milder levels in all the parameters analysed than their AB7-infected counterparts. The resolution of infection was earlier in 1B-infected mice and, although the immune response to both strains was Th1-like, a more intense CD8+ T-cell response and an earlier presence of TNF-alpha in serum were observed in this group. C. pecorum infection was controlled mainly by a non-specific immune response, since these mice showed no signs of a systemic specific immune response. Neutrophil depletion experiments showed that these cells play a very limited role in the non-specific response against C. pecorum.

摘要

在本研究中,使用CBA/J小鼠来确定对三种衣原体菌株免疫反应的差异:AB7(鹦鹉热衣原体野生型菌株)、1B(鹦鹉热衣原体疫苗株)和iB1(猪衣原体)。通过研究临床症状、从脾脏分离出的细菌数量以及肝脏病理,评估了每种菌株中衣原体感染的进展情况。然后研究了免疫反应的三个方面:肝脏中白细胞浸润的特征、脾脏中T细胞和B细胞、巨噬细胞及中性粒细胞的百分比,以及血清中细胞因子的存在情况。鹦鹉热衣原体感染的小鼠感染过程不同;与感染AB7的小鼠相比,感染1B的小鼠在所有分析参数中显示出较轻的水平。感染1B的小鼠感染消退更早,并且尽管对两种菌株的免疫反应均类似Th1型,但在该组中观察到更强烈的CD8 + T细胞反应以及血清中更早出现肿瘤坏死因子-α。猪衣原体感染主要由非特异性免疫反应控制,因为这些小鼠未显示出全身性特异性免疫反应的迹象。中性粒细胞耗竭实验表明,这些细胞在针对猪衣原体的非特异性反应中作用非常有限。

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