中国免疫学杂志
中國免疫學雜誌
중국면역학잡지
CHINESE JOURNAL OF IMMUNOLOGY
2015年
6期
803-805,821
,共4页
郭亚春%封桂英%宋鸿儒%邢恩鸿%安高%赵晓菲
郭亞春%封桂英%宋鴻儒%邢恩鴻%安高%趙曉菲
곽아춘%봉계영%송홍유%형은홍%안고%조효비
胶原诱导型关节炎%IL-17%IL-27%IL-10%流式细胞术
膠原誘導型關節炎%IL-17%IL-27%IL-10%流式細胞術
효원유도형관절염%IL-17%IL-27%IL-10%류식세포술
Collagen-induced arthritis%IL-17%IL-27%IL-10%Flow cytometry
目的::观察鸡Ⅱ型胶原诱导型关节炎( CIA)小鼠血清中IL-27、IL-17、IL-10的动态变化。方法:54只DBA1/J小鼠随机分为对照组(每组6只)和模型组(每组12只),分别在CIA小鼠病程进展的早、中、晚期无菌摘眼球取血,常规分离血清,应用流式细胞术检测各组小鼠在疾病病程的早、中、晚期血清中细胞因子IL-27、IL-17、IL-10的动态变化情况。结果:模型组IL-27在疾病早期、中期显著下降(P<0.05;P<0.01),疾病晚期与对照组比较差异无统计学意义(P>0.05);模型组IL-17在疾病的早期及晚期与对照组比较无明显区别( P>0.05),而在病程中期显著高于对照组( P<0.05)。 IL-10在CIA小鼠的病程进展中,模型组与对照组相比差异无明显区别(P>0.05)。结论:细胞因子IL-27和IL-17、IL-10可能参与CIA发病,可能与胶原诱导型关节炎的炎症进展有一定关系。
目的::觀察鷄Ⅱ型膠原誘導型關節炎( CIA)小鼠血清中IL-27、IL-17、IL-10的動態變化。方法:54隻DBA1/J小鼠隨機分為對照組(每組6隻)和模型組(每組12隻),分彆在CIA小鼠病程進展的早、中、晚期無菌摘眼毬取血,常規分離血清,應用流式細胞術檢測各組小鼠在疾病病程的早、中、晚期血清中細胞因子IL-27、IL-17、IL-10的動態變化情況。結果:模型組IL-27在疾病早期、中期顯著下降(P<0.05;P<0.01),疾病晚期與對照組比較差異無統計學意義(P>0.05);模型組IL-17在疾病的早期及晚期與對照組比較無明顯區彆( P>0.05),而在病程中期顯著高于對照組( P<0.05)。 IL-10在CIA小鼠的病程進展中,模型組與對照組相比差異無明顯區彆(P>0.05)。結論:細胞因子IL-27和IL-17、IL-10可能參與CIA髮病,可能與膠原誘導型關節炎的炎癥進展有一定關繫。
목적::관찰계Ⅱ형효원유도형관절염( CIA)소서혈청중IL-27、IL-17、IL-10적동태변화。방법:54지DBA1/J소서수궤분위대조조(매조6지)화모형조(매조12지),분별재CIA소서병정진전적조、중、만기무균적안구취혈,상규분리혈청,응용류식세포술검측각조소서재질병병정적조、중、만기혈청중세포인자IL-27、IL-17、IL-10적동태변화정황。결과:모형조IL-27재질병조기、중기현저하강(P<0.05;P<0.01),질병만기여대조조비교차이무통계학의의(P>0.05);모형조IL-17재질병적조기급만기여대조조비교무명현구별( P>0.05),이재병정중기현저고우대조조( P<0.05)。 IL-10재CIA소서적병정진전중,모형조여대조조상비차이무명현구별(P>0.05)。결론:세포인자IL-27화IL-17、IL-10가능삼여CIA발병,가능여효원유도형관절염적염증진전유일정관계。
Objective:To observe chicken typeⅡcollagen-induced arthritis( CIA) in serum of mice with the dynamic changes of IL-27,IL-17,IL-10. Methods: 54 DBA1/J mice were randomly divided into control group(n=6) and model group(n=12), according to the progress of CIA mouse course early,middle and late(7,14,and 35 days after booster immunization) ,taking the eyeball for blood and separating the serum under sterile condition. The dynamic levels of cytokines IL-27,IL-17,IL-10 were detected by flow cy-tometry. Results:The level of IL-27 in the model group was significantly declined in the the progress of CIA mouse course early and middle(P<0. 05,P<0. 01) compared with the control group,but there was no significant difference between late disease and control group(P> 0. 05);the level of IL-17 in the disease early and late was no significant difference(P> 0. 05) compared with the control group,while in the mid course significantly higher than control group(P<0. 05) during the course of disease. The level of IL-10 showed no difference from the experiment beginning(P> 0. 05). Conclusion: IL-27,IL-17,IL-10 paticipate in the pathogenesis of CIA and their alterations at different stages of the disease have a relation to the development of arthritis.