中国实用医刊
中國實用醫刊
중국실용의간
CENTRAL PLAINS MEDICAL JOURNAL
2014年
11期
32-34
,共3页
急性白血病%微小残留病变%DC-CIK%细胞因子
急性白血病%微小殘留病變%DC-CIK%細胞因子
급성백혈병%미소잔류병변%DC-CIK%세포인자
Acute leukemia%Minimal residual disease%DC-CIK%Cytokines
目的:分析41例急性白血病微小残留病变的DC-CIK细胞治疗前后实验室检测指标改变特点,探讨其临床治疗意义。方法33例急性髓细胞白血病( AML)患者均经MA方案(米托蒽醌、阿糖胞苷200 mg)或维甲酸/三氧化二砷诱导缓解,2例M2患者采用CAG方案(阿克拉霉素,阿糖胞苷,粒系集落刺激因子300μg/d)诱导缓解,8例急性淋巴细胞白血病患者均经VDCLP方案(长春新碱,柔红霉素,环磷酰胺,左旋门冬酰胺酶,泼尼松)诱导缓解。所有患者应用大剂量强化化疗方案缓解后用 DC-CIK交替维持治疗。结果 DC-CIK治疗后CD3﹢、CD3﹢CD8﹢、CD3﹢CD56﹢/CD16﹢细胞比例明显提高,差异有统计学意义。治疗后白细胞介素( IL)-2、IL-12、IL-17、肿瘤坏死因子-α、干扰素-γ水平提高,而IL-8水平降低,差异有统计学意义。治疗前后微小残留灶WT1的检测显示3例AML 患者治疗前WT1阳性,经DC-CIK 治疗后转阴。IL-17健康对照组最高,未缓解及初治白血病最低,缓解组逐渐升高,DC-CIK治疗后接近正常。结论 DC-CIK免疫治疗急性白血病清除微小残留病变能改善患者免疫抑制状态,提高机体的抗急性白血病免疫效应,有较好的临床疗效。
目的:分析41例急性白血病微小殘留病變的DC-CIK細胞治療前後實驗室檢測指標改變特點,探討其臨床治療意義。方法33例急性髓細胞白血病( AML)患者均經MA方案(米託蒽醌、阿糖胞苷200 mg)或維甲痠/三氧化二砷誘導緩解,2例M2患者採用CAG方案(阿剋拉黴素,阿糖胞苷,粒繫集落刺激因子300μg/d)誘導緩解,8例急性淋巴細胞白血病患者均經VDCLP方案(長春新堿,柔紅黴素,環燐酰胺,左鏇門鼕酰胺酶,潑尼鬆)誘導緩解。所有患者應用大劑量彊化化療方案緩解後用 DC-CIK交替維持治療。結果 DC-CIK治療後CD3﹢、CD3﹢CD8﹢、CD3﹢CD56﹢/CD16﹢細胞比例明顯提高,差異有統計學意義。治療後白細胞介素( IL)-2、IL-12、IL-17、腫瘤壞死因子-α、榦擾素-γ水平提高,而IL-8水平降低,差異有統計學意義。治療前後微小殘留竈WT1的檢測顯示3例AML 患者治療前WT1暘性,經DC-CIK 治療後轉陰。IL-17健康對照組最高,未緩解及初治白血病最低,緩解組逐漸升高,DC-CIK治療後接近正常。結論 DC-CIK免疫治療急性白血病清除微小殘留病變能改善患者免疫抑製狀態,提高機體的抗急性白血病免疫效應,有較好的臨床療效。
목적:분석41례급성백혈병미소잔류병변적DC-CIK세포치료전후실험실검측지표개변특점,탐토기림상치료의의。방법33례급성수세포백혈병( AML)환자균경MA방안(미탁은곤、아당포감200 mg)혹유갑산/삼양화이신유도완해,2례M2환자채용CAG방안(아극랍매소,아당포감,립계집락자격인자300μg/d)유도완해,8례급성림파세포백혈병환자균경VDCLP방안(장춘신감,유홍매소,배린선알,좌선문동선알매,발니송)유도완해。소유환자응용대제량강화화료방안완해후용 DC-CIK교체유지치료。결과 DC-CIK치료후CD3﹢、CD3﹢CD8﹢、CD3﹢CD56﹢/CD16﹢세포비례명현제고,차이유통계학의의。치료후백세포개소( IL)-2、IL-12、IL-17、종류배사인자-α、간우소-γ수평제고,이IL-8수평강저,차이유통계학의의。치료전후미소잔류조WT1적검측현시3례AML 환자치료전WT1양성,경DC-CIK 치료후전음。IL-17건강대조조최고,미완해급초치백혈병최저,완해조축점승고,DC-CIK치료후접근정상。결론 DC-CIK면역치료급성백혈병청제미소잔류병변능개선환자면역억제상태,제고궤체적항급성백혈병면역효응,유교호적림상료효。
Objective To analyze the change characteristics of laboratory test indexes before and after treatment with DC-CIK cells for 41 cases of acute leukemia minimal residual disease,and investigate its clinical significance. Methods Thirty-three cases of AML were treated with MA regimen( 200 mg mitoxantrone,Ara)remission induced by arsenic trioxide or retinoic acid,2 cases of M2 were treated with CAG scheme( Accra mycin,cytarabine,granulocyte colony-stimulating factor 300 μg/d)induction of remission,8 cases were treated with VDCLP regimen( vincristine,doxorubicin,cyclophosphamide, prednisone,L-asparaginase,)induced remission. All patients had remission with large dose of intensive chemotherapy,and then with DC-CIK alternating maintenance treatment. Results After DC-CIK treat-ment,the CD3 ﹢,CD3 ﹢ CD8 ﹢,CD3 ﹢ CD56 ﹢/CD16 ﹢ cell ratio significantly increased,the differences were significant. The levels of IL-2,IL-12,IL-17,TNF-α,IFN-γlevels increased after treatment,and the level of IL-8 decreased,there were significant differences. Detection of minimal residual foci of WT1 showed positive WT1 in 3 cases of AML patients before treatment. After treatment of DC and CIK, showed negative WT1. IL-17 level in healthy control group was the highest,and the lowest in patients with initial treatment and without remission leukemia,in remission group,IL-17 level gradually in-creased,after the treatment with DC-CIK,returned to normal range. Conclusions DC-CIK immune therapy in treatment of acute leukemia minimal residual disease can improve the removal of immunosup-pression in patients with acute leukemia,and improve the immunity,has good clinical curative effect.