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首页> 外文期刊>International Journal of Biomedical and Advance Research >Evaluation of Peritoneal Macrophages Migration Inhibition and Lymphocytes Mitotic Index in Shigella Dysenteriae Type1 Immunized Guinea Pigs
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Evaluation of Peritoneal Macrophages Migration Inhibition and Lymphocytes Mitotic Index in Shigella Dysenteriae Type1 Immunized Guinea Pigs

机译:痢疾志贺菌1型免疫豚鼠腹膜巨噬细胞迁移抑制和淋巴细胞有丝分裂指数的评估。

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Background and objective : To determine the performance and functional activity of macrophage and lymphocytes after immunization with phenol killed? Shigella dysenteriae type 1 Materials and Methods: ? phenol killed Shigella dysenteriae type 1 (16 ? 103bacteria /ml ) was injected subcutaneously(S/C)? in 10 guinea pigs at a dose of 0.5 ml .At the 3rd? week animals given a 1st? booster dose of (1 ml) of killed bacteria. At 5th?? week, a 2nd ?booster dose (1ml)? was given (S/C) . Five animals were used as control group and injected with phosphate buffer saline . After isolation of peritoneal macrophage and Blood Lymphocytes, macrophage migration inhibition (MMIT) and lymphocytes, transformation (LTT) tests have been applied. Results: The level of inhibition of migration decreased gradually, while reducing the concentration of the PHA antigen. Migration inhibition coefficient was (0.477 ? 0.268) when PHA antigen (400 ?g / ml) , (0.610 ? 0.181) when PHA (40 ?g / ml), (0.641 ? 0.145) when PHA antigen (4 ?g / ml). No significant difference in migration inhibition coefficient was detected between immunized groups (p value =0.118245) at different concentration of PHA antigen. The control group did not show any migration inhibition for macrophages at different concentrations of PHA antigen. Significant difference was detected between control groups (p value =0.033035) at different concentration of PHA antigen. Significant difference (p value =0.00759 ) , (p value =0.017049) , (p value =0.000278) was detected between immunized and control groups at 4 ?g / ml, 40 ?g / ml, 400 ?g / ml, concentration of PHA antigen respectively . Lymphocyte transformation test showed a clear response of the lymphocytes toward PHA . The mitotic index (Ml) of the lymphocytes? exposed to the (0.1mg/ml) PHA antigen was(11.56 ? 3.22 )and for (5mg/ml) PHA was (41.49 ? 26.298 )and for? control? was (1.18 ? 0.516).? Significant difference in mitotic index was detected between groups (p value =0.003554) according to the dose of PHA? antigen.? Conclusions: MMIT and LTT can be used effectively to evaluate and monitoring of immunological responsiveness to shigella dysenteriae type 1 antigen? and both MMIT and LTT proportionally associated with pre sensitization dose and duration of exposure to antigen .
机译:背景与目的:确定用酚杀死后免疫巨噬细胞和淋巴细胞的功能和功能?痢疾志贺氏菌1型材料和方法:皮下注射1次苯酚杀死的痢疾志贺氏菌1型(16→103细菌/ ml)?在10只豚鼠中,剂量为0.5毫升。在第三天?周动物给予第一?灭活细菌的加强剂量(1毫升)。在第五?一周,第二次“助推器剂量(1毫升)”?被给予(S / C)。 5只动物为对照组,注射磷酸盐缓冲盐水。分离腹膜巨噬细胞和血液淋巴细胞,巨噬细胞迁移抑制(MMIT)和淋巴细胞后,已应用转化(LTT)测试。结果:迁移抑制水平逐渐降低,同时降低了PHA抗原的浓度。 PHA抗原(400μg/ ml)时的迁移抑制系数为(0.477±0.268),PHA(40μg/ ml)时的迁移抑制系数为(0.610±0.181),PHA抗原(4μg/ ml)时的迁移抑制系数为(0.641±0.145)。 。在不同浓度的PHA抗原下,免疫组之间的迁移抑制系数没有显着差异(p值= 0.118245)。对照组在不同浓度的PHA抗原下对巨噬细胞没有任何迁移抑制作用。在不同浓度的PHA抗原下,对照组之间有显着差异(p值= 0.033035)。在免疫组和对照组之间分别以4微克/毫升,40微克/毫升,400微克/毫升, PHA抗原分别。淋巴细胞转化试验显示淋巴细胞对PHA有明显反应。淋巴细胞的有丝分裂指数(M1)?暴露于(0.1mg / ml)PHA抗原的浓度为(11.56±3.22),对于(5mg / ml)而言,PHA的浓度为(41.49×26.298),而对于(5mg / ml)PHA抗原的浓度为(41.49×26.298)。控制?是(1.18?0.516)。根据PHA剂量,两组之间的有丝分裂指数有显着差异(p值= 0.003554)。抗原。?结论:MMIT和LTT可有效地评估和监测对痢疾志贺氏菌1型抗原的免疫反应? MMIT和LTT均与致敏前剂量和暴露抗原的时间成正比。

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