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作 者:陈姝[1] 陆惠民[1] 高琪[2] 张山鹰 唐学恒[1] 孙臻安[1]
机构地区:[1]苏州大学医学院寄生虫学教研室,江苏苏州215007 [2]江苏省寄生虫病防治研究所 [3]福建省寄生虫病防治研究所
出 处:《中国寄生虫病防治杂志》2005年第3期172-174,共3页Chinese Journal of Parasitic Disease Control
基 金:江苏省自然科学基金资助项目(No.BK97157)。
摘 要:目的探讨IL12对伯氏疟原虫(P.b)红内期感染小鼠淋巴细胞增殖活性的影响。方法每只BALB/c小鼠接种5×105个感染P.b的RBC,同时每天分别给予0.03或0.15μgIL12处理,用3HTdR掺入法检测脾淋巴细胞增殖转化活性,流式细胞仪测定T淋巴细胞亚群CD4+与CD8+百分比。结果每天给予0.03或0.15μgIL12处理,均可显著增加P.b感染小鼠脾淋巴细胞数量及CD4+、CD8+数。每天给予0.03μgIL12可显著促进脾淋巴细胞的增殖转化,而每天给予0.15μgIL12则明显抑制脾淋巴细胞增殖。结论适当低剂量IL12可促进P.b感染小鼠脾淋巴细胞增殖活性,增强机体抗感染免疫,而较大剂量IL12则抑制脾淋巴细胞增殖活性,甚至可致免疫病理损害。Objective To explore the effects of IL12 on the splenic lymphocyte proliferation in mice with bloodstage Plasmodium berghei infection. Methods Each of BALB/c mice was infected with 5×10 5 RBC infected P. berghei and administrated with doses 0.03 or 0.15 μg/d of IL12 on the day of infection and daily for 6 days postinfection. The splenic lymphocyte proliferation was determined by 3 HTdR incorporation. Percentages of CD4 + and CD8 + T cells were detected using flow cytometry. Results Following IL12 administration, the mice treated with both doses 0.03 μg/d and 0.15 μg/d showed profound increasing in the number of splenic lymphocyte, as well as profound increasing in the absolute number and percentage of CD4 + and CD8 + T cells. Interestingly, treating with doses 0.03 μg/d of IL12 could significantly enhance splenic lymphocyte proliferative responses. In contrast, a 0.15 μg/d dose significantly inhibited lymphocyte proliferation. Conclusion Appropriate dose of IL12 regulated the development of resistance to P. berghei infection by enhancing splenic lymphocyte proliferative responses. But, higher doses of IL12 significantly inhibited lymphocyte proliferation, which may be detrimental to resistance against P. berghei infection.
关 键 词:白细胞介素12(IL-12) 疟原虫 伯氏 脾淋巴细胞增殖
分 类 号:R382.31[医药卫生—医学寄生虫学]
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