新型利什曼原虫主疫苗对Balb/c小鼠利什曼原虫攻击后免疫反应(血清IL-17、IL-23和脾脏白髓改变)的评价

A. Latifynia, M. Gharagozlou, A. Masood, R. Samani, S. Charedar, M. Mohebali
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引用次数: 0

摘要

利什曼原虫是一种原生动物寄生虫,其生命周期以无尾虫(在哺乳动物体内和巨噬细胞中间)和promastigote的形式存在于具有不同抗原决定位点的蚊子唾液和培养基中。目的:评价新型利什曼原虫主疫苗对利什曼原虫侵袭后血清IL-17和IL-23的抑制作用,以及再次暴露后活体小鼠的脾脏白髓变化。结果:100 μg/ml与200 μg/ml剂量组小鼠髓脾数量差异无统计学意义。LB组IL-17、IL-23和小鼠体重水平最低,MPS、PSW/MW、髓脾数和脾脏重量最高。LT组IL-23水平最高,平均牙髓大小和脾脏重量/小鼠百分比最低,脾脏重量几乎显著。LBT组IL-17水平最高。IL-23水平以LB组和对照组最低,脾重/鼠重百分比和髓脾数均以对照组最高。结论:LT组脾重量和髓脾数量均以辅助剂-磷酸铕最低,IL-23含量最高。可以认为,该佐剂优于卡介苗,可使小鼠表现出更强的免疫反应,可能在活的利什曼原虫攻击后产生Th1免疫反应和保护作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of New Leishmania Major Vaccine Against Immune Responses (Serum’s IL-17 and IL-23 and Spleen White Pulp Changes) Post Challenging with Leishmania Amastigotes in Balb/c Mice
Introduction: Leishmania is a protozoan parasite that has a life cycle in the form of an amastigote (in the mammalian body and in the middle of the macrophage) and promastigote in the mosquito saliva and culture medium with different antigenic determinant sites.Aim: Evaluation of new Leishmania major vaccine against serum’s IL-17 and IL-23 and spleen white pulp changes post challenging with Leishmania amastigotes survival rate of live mice was also evaluated for the second time after re-exposure.Result: Number of pulp spleen had almost significant differences between doses 100 and 200 μg/ml. LB group had lowest levels of IL-17, IL-23 and mouse weight and highest MPS, PSW/MW , number of pulp spleen and spleen weight was almost significant. LT group had highest levels of IL-23, whether, had lowest levels of mean pulp size, percent of spleen weight/mouse, and spleen weight was almost significant. LBT group had highest levels of IL-17. Lowest levels of IL-23 belonged to LB and control group and highest levels of percent of spleen weight/mouse weight and number of pulp spleen belong to control group also.Conclusion: In LT group, with adjuvant-Teucrium polium, weight of spleen and number of pulp spleen were at lowest level and had highest IL-23. It can be argued that this adjuvant was better than BCG and causes the mice to exhibit stronger immune responses that are likely to go Th1 immune response and protective effect after challenge with live Leishmania major.
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