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首页> 外文期刊>International immunopharmacology >Immunosuppressive effect of cyclophosphamide on white blood cells and lymphocyte subpopulations from peripheral blood of Balb/c mice.
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Immunosuppressive effect of cyclophosphamide on white blood cells and lymphocyte subpopulations from peripheral blood of Balb/c mice.

机译:BALB / C小鼠外周血与白细胞对白细胞和淋巴细胞亚群的免疫抑制作用。

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摘要

There has been lack of the uniform standard for establishment of animal immunodepressive models induced by cyclophosphamide (CTX), and the information about the immunosuppressive effect of CTX on peripheral blood lymphocyte subsets in rodents. Here we describe a CTX-induced mouse model and try to establish a feasible immunosuppressive model for studying the fungal pathogenicity. Balb/c mice received two intraperitoneal injections of different CTX doses (50-200 mg/kg) at 2-day intervals. Peripheral whole blood collected at different time-points before and after CTX injection was used to detect white blood cells (WBCs), lymphocytes and their subsets by automated hematology analyzer and flow cytometry, respectively. WBCs and lymphocytes in all groups except CTX50 (50 mg/kg CTX) group commenced to decrease in a dose-dependent manner on day 1, reached the nadir on day 4, rebounded on day 10, and declined again on day 17 after CTX treatment. Low dose (50 mg/kg) CTX produced no obvious change of percentage of CD3(+), CD4(+) and CD8(+) T cells and CD19(+) cells, but high doses (100 or 150 mg/kg) yielded a significant decrease of CD3(+) and CD4(+) cells on day 4 and CD19(+) cells on day 10, and increase of CD8(+) cells on day 4. The CD4(+)/CD8(+) ratio decreased on day 4, followed by a rebound thereafter when treated with 3 different doses of CTX. The results indicate that two intraperitoneal injections of CTX at 150 mg/kg at 2-day intervals may establish good immunosuppressive models of Balb/c mice for studying the fungal pathogenicity.
机译:缺乏用于建立由环磷酰胺(CTX)诱导的动物免疫抑制模型的统一标准,以及关于CTX在啮齿动物外周血淋巴细胞亚群的免疫抑制作用的信息。在这里,我们描述了一种CTX诱导的小鼠模型,并尝试建立一种用于研究真菌致病性的可行免疫抑制模型。 BALB / C小鼠以2天间隔接受两种腹腔注射不同的CTX剂量(50-200mg / kg)。在CTX注射之前和之后在不同时间点收集的外周整体用于通过自动血液分析仪和流式细胞术检测白细胞(WBCS),淋巴细胞及其子集。除了CTX50(50mg / kg CTX)组外的所有组中的WBC和淋巴细胞开始于第1天依赖于剂量依赖的方式,第4天达到Nadir,在第10天反弹,并在CTX治疗后第17天再次下降。低剂量(50mg / kg)CTX没有产生CD3(+),CD4(+)和CD8(+)T细胞和CD19(+)细胞百分比的明显变化,但高剂量(100或150mg / kg)在第4天和第4天和CD19(+)细胞上产生CD3(+)和CD4(+)细胞的显着降低,并在第4天增加CD8(+)细胞。CD4(+)/ CD8(+)在第4天的比率下降,然后在用3种不同剂量的CTX处理时,此后的反弹。结果表明,2天间隔的150mg / kg的CTX的两个腹腔注射可以建立用于研究真菌致病性的BALB / C小鼠的良好免疫抑制模型。

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