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作 者:范舒萍[1] 王艳红[1] 赵永华[2] 米洋[1] 侯星生[1] 王姝月[1] 邓志华[3] 罗旭光[1] 王桂琴[1]
机构地区:[1]山西医科大学微生物学与免疫学教研室,太原030001 [2]太原钢铁(集团)有限公司太钢总医院体检中心,030008 [3]山西医科大学第二附属医院消化科,太原030001
出 处:《免疫学杂志》2013年第5期387-390,共4页Immunological Journal
基 金:山西省科技攻关项目(20120313024-3)
摘 要:目的探讨髓样抑制细胞(myeloid-derived suppressor cells,MDSCs)在自身免疫性肝炎(autoimmune hepatitis,AIH)发生发展中的作用。方法用S-100建立C57BL/6小鼠AIH模型,随机将小鼠分为模型组和对照组,每组15只。从模型组和对照组C57BL/6小鼠的肝脏和骨髓中分离单个核细胞,用流式细胞术检测MDSCs数量变化。结果 CD11b+MDSCs在模型组小鼠的肝脏和骨髓中数量高于对照组(P<0.05),并且在骨髓中增高的比例显著大于肝脏,CD14+的细胞数量在模型组小鼠低于对照组的数量(P<0.05)。结论 AIH发生发展中MDSCs参与了局部的免疫调节作用。For investigating the role of myeloid-derived suppressor cells (MDSCs) in the development of autoimmune hepatitis (AIH), C57BL/6 mice were randomly divided into model group and control group, with 15 mice in each group in this research. AIH mouse model was established in C57BL/6 mice by using S-100. In model group and control group, mononuclear cells were separated from liver and bone marrow of mice, and analyzed by flow cytometry. The results showed the number of CDllb+ MDSCs in liver and bone marrow of AIH group were higher than those in the control group separately (P〈 0.05), and the proportion of increased CD111b+ MDSCs in bone marrow was significantly higher than those in liver. In the mean time, the count of CD14+ cells in AIH mice were less than that in control group (P〈 0.05). In conclusion, MDSCs may play a role in the development of AIH in local immunity.
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