肿瘤研究与临床
腫瘤研究與臨床
종류연구여림상
CANCER RESEARCH AND CLINIC
2011年
9期
588-590,597
,共4页
罗社文%毛积分%赵风翎%李哲%刘明贺%宋晓萍%许莉%张丹梅%高锦%王大鹏
囉社文%毛積分%趙風翎%李哲%劉明賀%宋曉萍%許莉%張丹梅%高錦%王大鵬
라사문%모적분%조풍령%리철%류명하%송효평%허리%장단매%고금%왕대붕
树突细胞%疫苗%杀伤细胞%细胞因子%抗原,肿瘤%流式细胞术%癌,非小细胞肺%免疫疗法,过继
樹突細胞%疫苗%殺傷細胞%細胞因子%抗原,腫瘤%流式細胞術%癌,非小細胞肺%免疫療法,過繼
수돌세포%역묘%살상세포%세포인자%항원,종류%류식세포술%암,비소세포폐%면역요법,과계
Dendritic cells%Vaccine%Killer cells%Cytokines%Antigens,neoplasms%Flow cytometry%Carcinoma,non-small-cell lung%Immunotherapy,adoptive
目的 观察自体肿瘤抗原负载的树突细胞(DCTAA)联合配型脐血来源的细胞因子诱导的杀伤细胞( CIK)免疫联合治疗48例中晚期肺癌的临床疗效。方法采用配型的脐血分离单个核细胞( PBMC),在体外用多种细胞因子[CD3McAb、白细胞介素(IL)-2、肿瘤坏死因子(IFN)-γ、IL-1 α等]共同诱导成CIK和树突细胞(DC),经过12-15 d诱导扩增后获得CIK细胞,再经严格质控检测合格后,分6次回输患者体内,每疗程回输细胞总数为(5-8) ×109个。培养的第5天用自体肿瘤抗原负载DC,第8天收获DCTAA,行淋巴结部位皮下注射,观察患者接受治疗后瘤体的大小、临床症状积分、生活质量及免疫学指标、Karnofsky评分、体质量、不良反应等的变化,同时记录患者的生存期。结果48例接受脐血DCTAA-CIK治疗的患者中,完全缓解(CR)+部分缓解(PR)为37例,总缓解率77.1%。临床症状评分改善率78.9%-84.7%;Karnofsky评分提高率为89.6%(43/48)。1年生存率80.6%。不良反应轻微。DCTAA-CIK细胞治疗患者外周血CD3、CD4T细胞和NK细胞比例均显著提高[(42.21 ±6.12)%、(24.42±3.01)%、0.99±0.34、(24.98±3.02)%与(71.58±7.64)%、(37.25±2.13)%、1.62±0.45、(35.23±4.11 )%](f值分别为6.34、5.67、0.25、4.43,P值均<0.01)。结论脐血来源的DCTAA-CIK细胞过继性免疫治疗是治疗中晚期肺癌的一种良好的方法,能显著提高患者免疫功能,改善患者临床症状,提高生存质量,延长生存期。
目的 觀察自體腫瘤抗原負載的樹突細胞(DCTAA)聯閤配型臍血來源的細胞因子誘導的殺傷細胞( CIK)免疫聯閤治療48例中晚期肺癌的臨床療效。方法採用配型的臍血分離單箇覈細胞( PBMC),在體外用多種細胞因子[CD3McAb、白細胞介素(IL)-2、腫瘤壞死因子(IFN)-γ、IL-1 α等]共同誘導成CIK和樹突細胞(DC),經過12-15 d誘導擴增後穫得CIK細胞,再經嚴格質控檢測閤格後,分6次迴輸患者體內,每療程迴輸細胞總數為(5-8) ×109箇。培養的第5天用自體腫瘤抗原負載DC,第8天收穫DCTAA,行淋巴結部位皮下註射,觀察患者接受治療後瘤體的大小、臨床癥狀積分、生活質量及免疫學指標、Karnofsky評分、體質量、不良反應等的變化,同時記錄患者的生存期。結果48例接受臍血DCTAA-CIK治療的患者中,完全緩解(CR)+部分緩解(PR)為37例,總緩解率77.1%。臨床癥狀評分改善率78.9%-84.7%;Karnofsky評分提高率為89.6%(43/48)。1年生存率80.6%。不良反應輕微。DCTAA-CIK細胞治療患者外週血CD3、CD4T細胞和NK細胞比例均顯著提高[(42.21 ±6.12)%、(24.42±3.01)%、0.99±0.34、(24.98±3.02)%與(71.58±7.64)%、(37.25±2.13)%、1.62±0.45、(35.23±4.11 )%](f值分彆為6.34、5.67、0.25、4.43,P值均<0.01)。結論臍血來源的DCTAA-CIK細胞過繼性免疫治療是治療中晚期肺癌的一種良好的方法,能顯著提高患者免疫功能,改善患者臨床癥狀,提高生存質量,延長生存期。
목적 관찰자체종류항원부재적수돌세포(DCTAA)연합배형제혈래원적세포인자유도적살상세포( CIK)면역연합치료48례중만기폐암적림상료효。방법채용배형적제혈분리단개핵세포( PBMC),재체외용다충세포인자[CD3McAb、백세포개소(IL)-2、종류배사인자(IFN)-γ、IL-1 α등]공동유도성CIK화수돌세포(DC),경과12-15 d유도확증후획득CIK세포,재경엄격질공검측합격후,분6차회수환자체내,매료정회수세포총수위(5-8) ×109개。배양적제5천용자체종류항원부재DC,제8천수획DCTAA,행림파결부위피하주사,관찰환자접수치료후류체적대소、림상증상적분、생활질량급면역학지표、Karnofsky평분、체질량、불량반응등적변화,동시기록환자적생존기。결과48례접수제혈DCTAA-CIK치료적환자중,완전완해(CR)+부분완해(PR)위37례,총완해솔77.1%。림상증상평분개선솔78.9%-84.7%;Karnofsky평분제고솔위89.6%(43/48)。1년생존솔80.6%。불량반응경미。DCTAA-CIK세포치료환자외주혈CD3、CD4T세포화NK세포비례균현저제고[(42.21 ±6.12)%、(24.42±3.01)%、0.99±0.34、(24.98±3.02)%여(71.58±7.64)%、(37.25±2.13)%、1.62±0.45、(35.23±4.11 )%](f치분별위6.34、5.67、0.25、4.43,P치균<0.01)。결론제혈래원적DCTAA-CIK세포과계성면역치료시치료중만기폐암적일충량호적방법,능현저제고환자면역공능,개선환자림상증상,제고생존질량,연장생존기。
Objective To observe the treatment effects in 48 cases of advanced lung cancer patients,with the immune therapy of the dendritic cells loading of tumor autologous antigen (DCTAA) combining with the cells induced factor of the killer cells (CIK) from the matched umbilical cord blood cells. Methods The peripheral blood mononuclear cell (PBMC) from the matched umbilical cord blood cells was seperated, and induced to CIK and DC with some cytokines in vitro, such as CD3McAb, IL-2, IFN-γ IL-1α, etc. After 12 to 15 days, the amplified CIK cells obtained were obtained, with the strict quality control, infused the CIK cells to the patients body back in six times, about (5-8)×109 CIK cells in each time. In the fifth day of the cultivation, DETAA cells were loaded and DCTAA cells were collected in the eighth day, and then hypodermic injection was done. The patient' s general situation after the immune treatment was observed, such as the size of the tumors, clinical symptom score, the quality of life and immune indexes. Karnofsky score, weight, toxic side effects and the patient's survival were also studied. Results In the 48 cases with the DCTAA-CIK treatment, complete remission (CR), partial remission (PR) was 37 cases, the overall remission rate was 77.1%. The improvement rate of clinical symptom scores was from 78.9 % to 84.7 %, the increasing rate of Karnofsky score was 89.6 % (43/48). 1-year survival reached to 80.6 %. There were significant difference in little toxic side effects(P < 0.01). The proportion of CD3, CD4 and NK cells in peripheral blood cells increased significantly (P < 0.01) after DCTAA-CIK cells treatment[(42.21±6.12)%, (24.42±3.01)%, 0.99±0.34, (24.98±3.02) %; (71.58±7.64) %, (37.25±2.13) %, 1.62±0.45, (35.23±4.11) %](t = 6.34, 5.67, 0.25, 4.43, P <0.01).Conclusion The DCTAA-CIK immune therapy is benefit for advanced lung cancer, not only improve the immune function but also ameliorate the clinical symptoms.