恩诺沙星治疗剂量对猪循环淋巴细胞亚群的影响

M. Pomorska-Mól, Z. Pejsak
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引用次数: 4

摘要

摘要选用20头遗传相似的猪(PIC)。试验猪随机分为试验组(ENRO, n = 10)和对照组(C, n = 10)。从第0天到第4天,ENRO组猪按推荐剂量给予恩诺沙星治疗。C组用PBS代替恩诺沙星。在研究的第0天(抗生素使用前)、第2天、第4天(抗生素使用期间)、第9天和第13天(恩诺沙星使用后)采集血样。采用血液学检查和流式细胞术建立各种白细胞亚群的相对和绝对计数。用荧光标记的抗体根据以下定义测量淋巴细胞亚群:CD3+ (T细胞)、CD21+ (B细胞)、CD4+CD8-(辅助性T细胞,Th)、CD4-CD8+(溶细胞T细胞,CLT)、CD4+CD8+(溶细胞和记忆T细胞)。本研究揭示了恩诺沙星对猪循环淋巴细胞组成的调节作用。与对照组相比,恩诺沙星治疗后CD8+细胞的浓度和百分比明显降低,CD4/CD8绝对比值显著升高(P < 0.05)。这些发现应该促使进一步研究所获得的结果在临床意义方面的实际意义。鉴于上述结果,不排除恩诺沙星也可能对宿主的感染反应具有免疫调节作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of therapeutic doses of enrofloxacin on circulating lymphocyte subpopulations in pigs
Abstract Twenty pigs of similar genetics (PIC) were used. Pigs were randomly divided into two groups: experimental (ENRO, n = 10) and control (C, n = 10). From day 0 to day 4, pigs from ENRO group received enrofloxacin at the recommended therapeutic dose. Pigs from C group received PBS instead of enrofloxacin. Blood samples were collected on days 0 (before antibiotic administration), 2, 4 (during antibiotic therapy), 9, and 13 of the study (after enrofloxacin administration). Haematological examination and flow cytometry were used to establish the relative and absolute counts of various leukocyte subsets. Lymphocyte subpopulations were measured by fluorochrom-labelled antibodies according to following definitions: CD3+ (T cells), CD21+ (B cells), CD4+CD8- (helper T cells, Th), CD4-CD8+ (cytolytic T cells, CLT), CD4+CD8+ (cytolytic and memory T cells). The present study revealed the modulating effect of enrofloxacin on the composition of circulating lymphocytes in pigs. Concentration and percentage of CD8+ cells decreased significantly after treatment with enrofloxacin and as a result the absolute CD4/CD8 ratio increased significantly as compared to control group (P < 0.05).These findings should prompt further studies on the practical significance of the results obtained in terms of clinical implications. In view of the results, it cannot be excluded that enrofloxacin may also have immunomodulatory effects on host response to infection.
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