摘要
目的:研究小剂量细胞因子在恶性肿瘤免疫治疗中的意义。方法:全身应用小剂量重组干扰素(IFNα2b)、白细胞介素-2(IL-2)和肿瘤坏死因子(α-TNF)联合治疗多种恶性肿瘤60例。应用APAAP法和免疫单向扩散法(RID)分析了治疗前后患者外周血中T、B淋巳细胞、NK细胞、免疫球蛋白(Ig)和补体C3活性。结果:治疗1个疗程后外周血中CD4+的T淋巴细胞和CD23+的B淋巴细胞显著的高于治疗前水平(P<0.05);CD4+/CD8+比值也明显增高(P<0.01)。免疫球蛋白(IgM)活性亦显著的高于治疗前水平(P<0.05)。KPS积分较治疗前明显增高(P<0.001)。治疗后细胞因子加化疗组的KPS积分平均增高28.5分(P<0.001);CR 26例(65.0%);PR 11例(27.5%),总有效率82.5%。单纯细胞因子治疗组的KPS积分平均增高23分(P<0.001);PR 13例(65.0%),总有效率65.0%。结论:本方案可以显著的提高多种恶性肿瘤患者的细胞免疫和体液免疫。有可能提高肿瘤的化疗效果和患者的生存质量,延长生存期。
ve:To study Clinical significance of the immuni - therapy on the patients with malignant tumor by the low dose recombinant α - IFN、IL- 2 and α- TNF. Methods:60 paitents with malignant tumor were treated by the minimal dose α IFN、 IL - 2 and α TNF;and to analyse the activity of T, B lymphocyte、NK cells and Ig、C3 in bloods of the patients with malignant tumor were easured by APAAP and RID. Results: The number of CD4± T- lymphocytes and CD23 ± Blymphocytes in bloods of the patients in back treatment was higher than the front treatment (P<0.05) ;the ratio of CD4 ± /CD8 ± T - limphocytes in back treatment also was significantly higher than the front treatment (P< 0.001) ;The activity of IgM also was significantly increased (P<0.05). The Karmorfaky integral in back treatment (mean 58.67± 14.43)was significantly higher than the front treatment (31.33± 11.99)(P <0.001). The middle and steady respones of the patients by cytoskine plus chemotherapy group was separate 65.0% and 27.5% . Conclusion: It was significant increased of cellular and humoral immunity function of an anti - carcinoma, the curative effected of chemotherapy and the quality of subsisted that of the patients of malignant tumor.
出处
《临床肿瘤学杂志》
CAS
2001年第4期317-319,共3页
Chinese Clinical Oncology