中国临床新医学
中國臨床新醫學
중국림상신의학
CHINESE JOURNAL OF NEW CLINICAL MEDICINE
2014年
4期
280-284
,共5页
钟永泷%林辉%蓝娇%李柏钧
鐘永瀧%林輝%藍嬌%李柏鈞
종영롱%림휘%람교%리백균
非小细胞肺癌%趋化因子受体%CD4阳性T淋巴细胞%T细胞亚群%趋化性
非小細胞肺癌%趨化因子受體%CD4暘性T淋巴細胞%T細胞亞群%趨化性
비소세포폐암%추화인자수체%CD4양성T림파세포%T세포아군%추화성
Non small cell lung cancer%Chemokine receptor%CD4-positive T-lymphocyte%T lympho-cyte subsets%Chemotaxis
目的:探讨CC族趋化因子受体9( CCR9)在非小细胞肺癌( NSCLC )肿瘤免疫机制中的作用。方法采用流式细胞术检测42例NSCLC患者和30名健康人手术前后T细胞亚群以及外周血中CD4+T淋巴细胞表面CCR9的表达情况,计数各组细胞表达的百分率。免疫磁珠分选外周血CD4+T淋巴细胞,采用transwell实验检测并分析CCL25/CCR9对CD4+T淋巴细胞迁移的影响。结果 NSCLC患者外周血T淋巴细胞亚群均降低,术后外周血CD4+T淋巴细胞、CD4+/CD8+比值均明显高于术前[(49.11±8.32) vs (46.17±8.71),P=0.031和(1.66±0.09) vs (1.44±0.06),P=0.001];术前CD4+CCR9+T淋巴细胞的百分率低于术后[(3.33±1.11) vs (6.57±1.92),P<0.05]和健康对照组[(3.33±1.11) vs (11.06±1.37),P<0.05]。在CCL25诱导下,NSCLC患者外周血CD4+T淋巴细胞趋化指数(CI)为3.14,明显低于健康对照组的3.83( P<0.05)。经过anti-CCR9单抗处理后,CD4+T淋巴细胞的CI为0.62,与未经anti-CCR9 mAb处理者相比明显降低( P<0.05)。结论 NSCLC患者外周血T淋巴细胞调节机制紊乱,CL25/CCR9相互作用可介导外周血CD4+T淋巴细胞迁移,NSCLC患者外周血淋巴细胞中CCR9低表达,影响淋巴细胞迁移,可能与肿瘤逃避免疫监视的机制有关。手术可以逆转CD4+T淋巴细胞表面CCR9的表达变化, CCR9可能作为评价肺癌治疗后免疫重建的指标。
目的:探討CC族趨化因子受體9( CCR9)在非小細胞肺癌( NSCLC )腫瘤免疫機製中的作用。方法採用流式細胞術檢測42例NSCLC患者和30名健康人手術前後T細胞亞群以及外週血中CD4+T淋巴細胞錶麵CCR9的錶達情況,計數各組細胞錶達的百分率。免疫磁珠分選外週血CD4+T淋巴細胞,採用transwell實驗檢測併分析CCL25/CCR9對CD4+T淋巴細胞遷移的影響。結果 NSCLC患者外週血T淋巴細胞亞群均降低,術後外週血CD4+T淋巴細胞、CD4+/CD8+比值均明顯高于術前[(49.11±8.32) vs (46.17±8.71),P=0.031和(1.66±0.09) vs (1.44±0.06),P=0.001];術前CD4+CCR9+T淋巴細胞的百分率低于術後[(3.33±1.11) vs (6.57±1.92),P<0.05]和健康對照組[(3.33±1.11) vs (11.06±1.37),P<0.05]。在CCL25誘導下,NSCLC患者外週血CD4+T淋巴細胞趨化指數(CI)為3.14,明顯低于健康對照組的3.83( P<0.05)。經過anti-CCR9單抗處理後,CD4+T淋巴細胞的CI為0.62,與未經anti-CCR9 mAb處理者相比明顯降低( P<0.05)。結論 NSCLC患者外週血T淋巴細胞調節機製紊亂,CL25/CCR9相互作用可介導外週血CD4+T淋巴細胞遷移,NSCLC患者外週血淋巴細胞中CCR9低錶達,影響淋巴細胞遷移,可能與腫瘤逃避免疫鑑視的機製有關。手術可以逆轉CD4+T淋巴細胞錶麵CCR9的錶達變化, CCR9可能作為評價肺癌治療後免疫重建的指標。
목적:탐토CC족추화인자수체9( CCR9)재비소세포폐암( NSCLC )종류면역궤제중적작용。방법채용류식세포술검측42례NSCLC환자화30명건강인수술전후T세포아군이급외주혈중CD4+T림파세포표면CCR9적표체정황,계수각조세포표체적백분솔。면역자주분선외주혈CD4+T림파세포,채용transwell실험검측병분석CCL25/CCR9대CD4+T림파세포천이적영향。결과 NSCLC환자외주혈T림파세포아군균강저,술후외주혈CD4+T림파세포、CD4+/CD8+비치균명현고우술전[(49.11±8.32) vs (46.17±8.71),P=0.031화(1.66±0.09) vs (1.44±0.06),P=0.001];술전CD4+CCR9+T림파세포적백분솔저우술후[(3.33±1.11) vs (6.57±1.92),P<0.05]화건강대조조[(3.33±1.11) vs (11.06±1.37),P<0.05]。재CCL25유도하,NSCLC환자외주혈CD4+T림파세포추화지수(CI)위3.14,명현저우건강대조조적3.83( P<0.05)。경과anti-CCR9단항처리후,CD4+T림파세포적CI위0.62,여미경anti-CCR9 mAb처리자상비명현강저( P<0.05)。결론 NSCLC환자외주혈T림파세포조절궤제문란,CL25/CCR9상호작용가개도외주혈CD4+T림파세포천이,NSCLC환자외주혈림파세포중CCR9저표체,영향림파세포천이,가능여종류도피면역감시적궤제유관。수술가이역전CD4+T림파세포표면CCR9적표체변화, CCR9가능작위평개폐암치료후면역중건적지표。
Objective To investigate the expression of CC chemokine receptor 9 ( CCR9 ) on peripheral blood CD4 +T lymphocyte cells of non small cell lung cancer ( NSCLC), and the effect of CCR9 and its ligand (CCL25) on peripheral blood CD4+T lymphocytes.Methods The study was performed in 42 NSCLC patients and 30 healthy controls .Flow cytometry was employed to detect the T lymphocyte subsets and the expression of CCR 9 on peripheral blood CD4 +T cells.Peripheral blood CD4 +T lymphocytes were isolated from all cases with magnetic-acti-vated cell sorting method .The cell trans-membrane test with 24-transwell was used to detect the effect of CCR 9/CCL25 on the lymphocyte migration .Results Compared with control group , the T lymphocyte subsets in pre-opera-tive patients were higher than that in post-operative patients(P<0.05).The frequency of CD4 +CCR9+T lympho-cyte in pre-operative group was both significantly decreased compared with post-operative group(3.33 ±1.11 vs 6.57 ± 1.92,P<0.05) and controls(3.33 ±1.11 vs 11.06 ±1.37,P<0.05).In the induce of CCL25, the chemotactic indexes(CI) of CD4 +T lymphocytes from NSCLC patients (3.14) was significantly lower than that from healthy per-sons(3.83).After anti-CCR9 mAb pretreatment, the lymphocytes CIs of NSCLC patients decreased significantly to 0.62 as compared with untreated controls .Conclusion The expression of CCR9 is down-regulated on NSCLC periph-eral blood CD4+T lymphocyte cells .CCR9/CCL25 interactions mediate the migration of CD 4 +T lymphocytes in bodies .The decreased expression of CCR 9 in the CD4+T lymphocytes of patients with NSCLC could effect the ability of lymphocytes migration , which might involve in the mechanisms of tumor escape immune surveillance .Operation could reverse the change of CCR 9 expression on CD4 +T lymphocyte cells .CCR9 may be suggested to indicate immu-nologic reconstitution after therapy and operation .