河北医学
河北醫學
하북의학
HEBEI MEDICINE
2015年
1期
134-137
,共4页
黄亚琼%赵庆丽%张锋军%顾丽萍
黃亞瓊%趙慶麗%張鋒軍%顧麗萍
황아경%조경려%장봉군%고려평
乳腺癌%吲哚胺2,3-双加氧酶%免疫耐受%CD33+MDSCs%Foxp3+Tregs
乳腺癌%吲哚胺2,3-雙加氧酶%免疫耐受%CD33+MDSCs%Foxp3+Tregs
유선암%신타알2,3-쌍가양매%면역내수%CD33+MDSCs%Foxp3+Tregs
Breast cancer%Indoleamine 2,3-dioxygenase%Immune tolerance%CD33+MDSCs%Foxp3+Tregs
目的:研究乳腺癌CD33+髓系来源的抑制细胞( MDSCs)中吲哚胺2,3-双加氧酶( IDO)表达情况及与Foxp3+调节性T细胞(Tregs)分布关系和临床意义。方法:运用免疫组化单染技术检测CD33+MDSCs细胞、Foxp3+Tregs,采用免疫组化双染检测CD33+MDSCs细胞中IDO的表达情况。结果:癌组织中CD33+MDSCs细胞、Foxp3+Tregs分布无序,呈散在分布;Foxp3+Tregs高比例组中,CD33+MD-SCs细胞中IDO呈高表达,差异有统计学意义( P<0.05);CD33+MDSCs中IDO的表达与患者年龄、肿瘤直径和组织学分级无明显关系,但与是否有淋巴结转移有密切关系( P<0.05)。结论:乳腺癌中CD33+MDSCs中IDO高表达参与肿瘤细胞免疫耐受的形成,可能与乳腺癌淋巴转移存在密切联系。
目的:研究乳腺癌CD33+髓繫來源的抑製細胞( MDSCs)中吲哚胺2,3-雙加氧酶( IDO)錶達情況及與Foxp3+調節性T細胞(Tregs)分佈關繫和臨床意義。方法:運用免疫組化單染技術檢測CD33+MDSCs細胞、Foxp3+Tregs,採用免疫組化雙染檢測CD33+MDSCs細胞中IDO的錶達情況。結果:癌組織中CD33+MDSCs細胞、Foxp3+Tregs分佈無序,呈散在分佈;Foxp3+Tregs高比例組中,CD33+MD-SCs細胞中IDO呈高錶達,差異有統計學意義( P<0.05);CD33+MDSCs中IDO的錶達與患者年齡、腫瘤直徑和組織學分級無明顯關繫,但與是否有淋巴結轉移有密切關繫( P<0.05)。結論:乳腺癌中CD33+MDSCs中IDO高錶達參與腫瘤細胞免疫耐受的形成,可能與乳腺癌淋巴轉移存在密切聯繫。
목적:연구유선암CD33+수계래원적억제세포( MDSCs)중신타알2,3-쌍가양매( IDO)표체정황급여Foxp3+조절성T세포(Tregs)분포관계화림상의의。방법:운용면역조화단염기술검측CD33+MDSCs세포、Foxp3+Tregs,채용면역조화쌍염검측CD33+MDSCs세포중IDO적표체정황。결과:암조직중CD33+MDSCs세포、Foxp3+Tregs분포무서,정산재분포;Foxp3+Tregs고비례조중,CD33+MD-SCs세포중IDO정고표체,차이유통계학의의( P<0.05);CD33+MDSCs중IDO적표체여환자년령、종류직경화조직학분급무명현관계,단여시부유림파결전이유밀절관계( P<0.05)。결론:유선암중CD33+MDSCs중IDO고표체삼여종류세포면역내수적형성,가능여유선암림파전이존재밀절련계。
Objective:To study the expression of indoleamine 2,3-dioxygenase ( IDO) in CD33+mye-loid-derived suppressor cells ( MDSCs) and the relationships between the expression of IDO and Foxp 3+reg-ulatory T cells ( Tregs) distribution and clinical significance. Method:Immunohistochemical single staining technique was used to detect CD33+MDSCs cells and Foxp3+Tregs.The immunohistochemical double staining was used to detect CD33+MDSCs cells indoleamine 2,3-bis dioxygenase (IDO) expression.Result:Carci-noma CD33+MDSCs cells, Foxp3+Tregs distribution were disorder and scattered in carcinoma. It showed sig-nificant difference between the expression of MDSCs IDO and Tregs distribution ( P<0.05). The expression of CD33+MDSCs in IDO had no relation with breast cancer , irrespective of age , tumor size and histological grade were coreelated with whether lymph node metastasis (P<0.05).Conclusion:It showed a close contact between carcinoma CD 33+MDSCs IDO expression in tumor cells and the formation of immune tolerance. Car-cinoma CD33+MDSCs IDO expression may be associated with the presence of lymph node metastasis.