南方医科大学学报
南方醫科大學學報
남방의과대학학보
JOURNAL OF SOUTHERN MEDICAL UNIVERSITY
2015年
4期
602-605
,共4页
石强%田成林%刘洁晓%蒲传强
石彊%田成林%劉潔曉%蒲傳彊
석강%전성림%류길효%포전강
自身免疫性肌炎%CD4+CD25+Foxp3+Treg细胞%流式细胞仪%IL-10%TGF-β%PD-1%CTLA-4
自身免疫性肌炎%CD4+CD25+Foxp3+Treg細胞%流式細胞儀%IL-10%TGF-β%PD-1%CTLA-4
자신면역성기염%CD4+CD25+Foxp3+Treg세포%류식세포의%IL-10%TGF-β%PD-1%CTLA-4
autoimmune myositis%CD4+CD25+Foxp3+Tregs%flow cytometry%IL-10%TGF-β%PD-1%CTLA-4
目的:探讨CD4+CD25+Foxp3+Treg细胞对于实验性自身免疫性肌炎(EAM)小鼠的治疗价值及机制。方法免疫磁珠分选技术从BALC/c小鼠脾脏中分选出足量CD4+CD25+Foxp3+Treg细胞以备回输,观察干预组及未干预组EAM小鼠肌肉组织病理学变化,流式细胞仪检测两组小鼠脾脏CD4+CD25+Foxp3+Treg细胞表面PD-1及CTLA-4的表达变化,双抗体夹心ELISA法检测外周血IL-10、TGF-β的变化。结果干预组小鼠较未干预组肌肉病理炎性细胞浸润明显减轻,其外周血IL-10、TGF-β含量较未干预组明显升高(P<0.05),脾脏CD4+CD25+Foxp3+Treg细胞表面PD-1及CTLA-4表达明显升高(P<0.05)。结论CD4+CD25+Foxp3+Treg细胞回输对于EAM小鼠的治疗效果是通过增加外周血IL-10及TGF-β水平和增高脾脏CD4+CD25+Foxp3+Treg细胞表面PD-1及CTLA-4的表达发挥作用。
目的:探討CD4+CD25+Foxp3+Treg細胞對于實驗性自身免疫性肌炎(EAM)小鼠的治療價值及機製。方法免疫磁珠分選技術從BALC/c小鼠脾髒中分選齣足量CD4+CD25+Foxp3+Treg細胞以備迴輸,觀察榦預組及未榦預組EAM小鼠肌肉組織病理學變化,流式細胞儀檢測兩組小鼠脾髒CD4+CD25+Foxp3+Treg細胞錶麵PD-1及CTLA-4的錶達變化,雙抗體夾心ELISA法檢測外週血IL-10、TGF-β的變化。結果榦預組小鼠較未榦預組肌肉病理炎性細胞浸潤明顯減輕,其外週血IL-10、TGF-β含量較未榦預組明顯升高(P<0.05),脾髒CD4+CD25+Foxp3+Treg細胞錶麵PD-1及CTLA-4錶達明顯升高(P<0.05)。結論CD4+CD25+Foxp3+Treg細胞迴輸對于EAM小鼠的治療效果是通過增加外週血IL-10及TGF-β水平和增高脾髒CD4+CD25+Foxp3+Treg細胞錶麵PD-1及CTLA-4的錶達髮揮作用。
목적:탐토CD4+CD25+Foxp3+Treg세포대우실험성자신면역성기염(EAM)소서적치료개치급궤제。방법면역자주분선기술종BALC/c소서비장중분선출족량CD4+CD25+Foxp3+Treg세포이비회수,관찰간예조급미간예조EAM소서기육조직병이학변화,류식세포의검측량조소서비장CD4+CD25+Foxp3+Treg세포표면PD-1급CTLA-4적표체변화,쌍항체협심ELISA법검측외주혈IL-10、TGF-β적변화。결과간예조소서교미간예조기육병리염성세포침윤명현감경,기외주혈IL-10、TGF-β함량교미간예조명현승고(P<0.05),비장CD4+CD25+Foxp3+Treg세포표면PD-1급CTLA-4표체명현승고(P<0.05)。결론CD4+CD25+Foxp3+Treg세포회수대우EAM소서적치료효과시통과증가외주혈IL-10급TGF-β수평화증고비장CD4+CD25+Foxp3+Treg세포표면PD-1급CTLA-4적표체발휘작용。
Objective To investigate effect of CD4+CD25+Foxp3+Tregs in the treatment of autoimmune myositis (EAM) in mice and explore the possible mechanisms. Methods Mouse models of EAM were divided randomly into model group and treatment group, and the latter received infusion of CD4 + CD25 + Foxp3 + Tregs separated from normal mouse spleen by magnetic activated cell sorting. The changes of muscle pathology was observed, and the expression of PD-1 and CTLA-4 in spleen CD4+ CD25+ Foxp3+ Tregs was analyzed using flow cytometry; peripheral blood IL-10 and TGF-β levels were tested using double antibody sandwich ELISA. Results Compare with the model group, the mice in the treatment group showed significantly reduced muscular inflammatory cell infiltration, increased blood levels of IL-10 and TGF-β (P<0.05), and increased expression of PD-1 and CTLA-4 in spleen CD4+CD25+Foxp3+Tregs (P<0.05). Conclusion CD4+CD25+Foxp3+Tregs reinfusion produces therapeutic effect in mice with EAM by increasing peripheral blood IL-10 and TGF-βlevels and PD-1 and CTLA-4 expressions in spleen CD4+CD25+Foxp3+Tregs.