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作 者:姚德茂[1] 潘承恩[1] 王一理[2] 司履生[2] 孟绍青[1]
机构地区:[1]西安医科大学第一附属医院外科,西安市710061 [2]西安医科大学免疫病理研究室
出 处:《中国肿瘤临床》1997年第5期339-342,共4页Chinese Journal of Clinical Oncology
基 金:陕西省卫生厅科研基金
摘 要:对20例经手术切除的进展期肿瘤患者用活化的自身肿瘤浸润淋巴细胞(TIL)和重组人白细胞介素-2(rhIL-2)治疗,并检测治疗前后细胞免疫变化。患者的PBL对同种异体相同组织学类型靶细胞的细胞毒性明显升高(P<0.05),而对无关靶细胞的细胞毒性无明显变化(P>0.05);外周血淋巴细胞产生IL-2的能力均有明显的提高,从12.3U/ml到19.8U/ml(P<0.01);对植物血凝素(PHA)皮试反应性明显增强,反应直径从8.6mm升高到13.5mm(P<0.01)。TIL输注过程中,11例有一过性寒战、发热(T<38℃),其中6例伴轻度恶心、呕吐。结果提示:单次输注TIL和小剂量rhIL-2综合治疗后,可明显提高进展期肿瘤患者的细胞免疫功能,而无严重毒副作用,可能成为进展期肿瘤术后重要的辅助治疗方法。Twenty cases of advanced cancers of stomach,liver,bladder were treated with activated auto-tumor-infiltrating lymphocytes (TIL) isolated from the patients themselves and supplemented by reconbinant interleukin-2 (rIL-2). Cellular immune response was assayed before and after TIL infusion. The results revealed that cytotoxicity was much elevated (P<0. 05). There was no significant change in cytotoxicity to histologically unrelated target cell lines (P>0. 05). Serum IL-2 level was elevated markedly (12. 3U/ml to 19. 8U/ml, P<0. 01 ). PHA skin test turned positive and the skin reaction lesion enlarged (PHA: 8, 6 mm to 13. 5 mm,P<0. 01 ). Eleven patients had transient chill and fever (T<38℃); and mild nausea and vomiting were seen in 6 of them during the TIL infusion. All these results indicate that TIL plus low-dose rIL-2 are able to improve cellular immunity in patients with advanced cancer without side-effect. It may play an important role in preventing recurrence and metastasis.
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