中华器官移植杂志
中華器官移植雜誌
중화기관이식잡지
CHINESE JOURNAL OF ORGAN TRANSPLANTATION
2013年
1期
47-51
,共5页
李永海%张淦%水丽君%房爱芳%郭峰%向莹%张伟杰
李永海%張淦%水麗君%房愛芳%郭峰%嚮瑩%張偉傑
리영해%장감%수려군%방애방%곽봉%향형%장위걸
胰岛移植%T淋巴细胞,调节%糖尿病,1型
胰島移植%T淋巴細胞,調節%糖尿病,1型
이도이식%T림파세포,조절%당뇨병,1형
Islets of Langerhans%T-Lymphocytes,regulatory%Diabetes mellitus,type 1
目的 探讨输注胰岛抗原特异性调节性T淋巴细胞(Treg细胞)对非肥胖糖尿病(NOD)小鼠同系胰岛移植物存活时间的影响.方法·以未成熟树突状细胞(imDC)联合谷氨酸脱羧酶-65在体外诱导童贞T淋巴细胞分化成胰岛抗原特异性Treg细胞.以已发生糖尿病的NOD小鼠为受者,将分离得到的尚未进展为糖尿病的NOD小鼠的胰岛(500胰岛当量)移植至受者的肾包膜下,对照组不行移植,只观察血糖变化;单纯胰岛移植组只进行胰岛移植,不输注胰岛抗原特异性Treg细胞;实验组于术前1d静脉输注1×106个胰岛抗原特异性Treg细胞,然后进行胰岛移植.术后检测受者的血糖,以判断移植胰岛的存活时间,观察胰岛移植物的病理学变化.结果 对照组血糖持续高于11.1 mmol/L;单纯胰岛移植组小鼠的血糖于术后1~2 d降至正常,到7~17d时开始陆续升高,并维持在术前水平,移植物存活时间为(12.2±2.6)d;实验组小鼠的血糖于术后1~2 d降至正常,至第27天开始有小鼠血糖升高超过11.1 mmol/L,第43天时,所有小鼠的血糖均超过11.1mmol/L,移植物的存活时间为(35.2±4.3)d,明显长于单纯胰岛移植组(P<0.01).单纯胰岛移植组的移植胰岛有明显的淋巴细胞浸润,并伴有胰岛细胞严重破坏,胰岛素染色未见完整的胰岛存在,仅有极少量残存的分泌胰岛素的胰岛细胞;实验组第15天时移植胰岛形态完整,仅有少量淋巴细胞浸润,分泌胰岛素的胰岛大量存在.结论 体外诱导产生的胰岛抗原特异性Treg细胞可以延缓自身免疫系统对移植胰岛的破坏,明显延长NOD小鼠移植胰岛的存活时间.
目的 探討輸註胰島抗原特異性調節性T淋巴細胞(Treg細胞)對非肥胖糖尿病(NOD)小鼠同繫胰島移植物存活時間的影響.方法·以未成熟樹突狀細胞(imDC)聯閤穀氨痠脫羧酶-65在體外誘導童貞T淋巴細胞分化成胰島抗原特異性Treg細胞.以已髮生糖尿病的NOD小鼠為受者,將分離得到的尚未進展為糖尿病的NOD小鼠的胰島(500胰島噹量)移植至受者的腎包膜下,對照組不行移植,隻觀察血糖變化;單純胰島移植組隻進行胰島移植,不輸註胰島抗原特異性Treg細胞;實驗組于術前1d靜脈輸註1×106箇胰島抗原特異性Treg細胞,然後進行胰島移植.術後檢測受者的血糖,以判斷移植胰島的存活時間,觀察胰島移植物的病理學變化.結果 對照組血糖持續高于11.1 mmol/L;單純胰島移植組小鼠的血糖于術後1~2 d降至正常,到7~17d時開始陸續升高,併維持在術前水平,移植物存活時間為(12.2±2.6)d;實驗組小鼠的血糖于術後1~2 d降至正常,至第27天開始有小鼠血糖升高超過11.1 mmol/L,第43天時,所有小鼠的血糖均超過11.1mmol/L,移植物的存活時間為(35.2±4.3)d,明顯長于單純胰島移植組(P<0.01).單純胰島移植組的移植胰島有明顯的淋巴細胞浸潤,併伴有胰島細胞嚴重破壞,胰島素染色未見完整的胰島存在,僅有極少量殘存的分泌胰島素的胰島細胞;實驗組第15天時移植胰島形態完整,僅有少量淋巴細胞浸潤,分泌胰島素的胰島大量存在.結論 體外誘導產生的胰島抗原特異性Treg細胞可以延緩自身免疫繫統對移植胰島的破壞,明顯延長NOD小鼠移植胰島的存活時間.
목적 탐토수주이도항원특이성조절성T림파세포(Treg세포)대비비반당뇨병(NOD)소서동계이도이식물존활시간적영향.방법·이미성숙수돌상세포(imDC)연합곡안산탈최매-65재체외유도동정T림파세포분화성이도항원특이성Treg세포.이이발생당뇨병적NOD소서위수자,장분리득도적상미진전위당뇨병적NOD소서적이도(500이도당량)이식지수자적신포막하,대조조불행이식,지관찰혈당변화;단순이도이식조지진행이도이식,불수주이도항원특이성Treg세포;실험조우술전1d정맥수주1×106개이도항원특이성Treg세포,연후진행이도이식.술후검측수자적혈당,이판단이식이도적존활시간,관찰이도이식물적병이학변화.결과 대조조혈당지속고우11.1 mmol/L;단순이도이식조소서적혈당우술후1~2 d강지정상,도7~17d시개시륙속승고,병유지재술전수평,이식물존활시간위(12.2±2.6)d;실험조소서적혈당우술후1~2 d강지정상,지제27천개시유소서혈당승고초과11.1 mmol/L,제43천시,소유소서적혈당균초과11.1mmol/L,이식물적존활시간위(35.2±4.3)d,명현장우단순이도이식조(P<0.01).단순이도이식조적이식이도유명현적림파세포침윤,병반유이도세포엄중파배,이도소염색미견완정적이도존재,부유겁소량잔존적분비이도소적이도세포;실험조제15천시이식이도형태완정,부유소량림파세포침윤,분비이도소적이도대량존재.결론 체외유도산생적이도항원특이성Treg세포가이연완자신면역계통대이식이도적파배,명현연장NOD소서이식이도적존활시간.
Objective To investigate the survival of islet isograft in NOD mice treated with islet antigen-specific regulatory T cells.Methods GAD-65 antigen pulsed immature dendritic cells (imDC) were used to induce naive T cells into islet antigen-specific regulatory T cells.NOD mice which had progressed to type 1 diabetes (T1DM),as the recipients,received islet isografts (500 IEQ) under renal capsule from NOD mice without T1DM.In NOD mice in control group without transplantation,the changes in blood glucose (BG) were observed.NOD mice in simple islet transplantation group were given islet isograft without Treg infusion.In experiment group,NOD mice were infused with 1 × 106 islet antigen-specific regulatory T cells on the 1st day before transplantation,subsequently underwent islet isotransplantation.The survival of the islet isograft was evaluated by BG levels and the pathological changes were observed.Results BG levels were sustained above 11.1 mmol/L in control group.In simple islet transplantation group,BG level was decreased to the normal level in 1 ~2 days after transplantation,and began to rebound in 7~ 17 days posttransplantation and maintained at the preoperative level.The mean survival of the islet isograft in the NOD mice was (12.2 ± 2.6) day;In experiment group,BG level was decreased to the normal level in 1 ~2 days after transplantation,rebounded above 11.1 mmol/L in some mice on the 27th day after transplantation,and rebounded above 11.1 rnmol/L on the 43th day in all mice.The mean survival of the islet isograft in the NOD mice was (35.2 ± 4.3) days,which was significantly prolonged compared to simple islet transplantation group (P< 0.01).In simple islet transplantation group,the islet isograft was infiltrated by many lymph cells and damaged severely,and only few residual islet cells secreted insulin without complete islet existing in insulin staining.The islet isograft in experiment group was intact on the 15th day,with little lymph cell infiltration and a great number of islets secreting insulin.Conclusion Infusion of islet antigen-specific regulatory T cells induced by imDC and islet antigen GAD-65 in vitro could delay the destruction of autoimmune system and prolong the islet isograft survival in NOD mice.