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作 者:康红刚[1] 王运良[1] 于津浦[1] 曹水[1] 任宝柱[1] 张新伟[1] 张维红[1] 韩颖[1] 任秀宝[1]
机构地区:[1]天津医科大学肿瘤医院生物治疗科,天津市肿瘤防治重点实验室,天津300060
出 处:《天津医科大学学报》2009年第3期362-365,375,共5页Journal of Tianjin Medical University
基 金:天津市科技创新专项资金资助(06FZZDSF01500)
摘 要:目的:探讨粒巨细胞集落刺激因子(GM-CSF)联合异体肿瘤细胞疫苗的安全性和有效性。方法:收录病理明确的IV期癌症患者60例,其中恶性黑色素瘤11例,卵巢癌10例,肾癌15例,胃/结直肠癌14例,乳腺癌10例。每周皮下注射肿瘤细胞和GM-CSF分泌细胞混合物1ml;共6次。在第1,5次注射同时,进行DTH接种试验。治疗前后取外周血样进行淋巴细胞亚型及细胞因子检测。治疗完成1个月后进行影像学检查。结果:所有病人对治疗耐受良好,无脱组患者。主要不良反应为,注射局部红肿疼痛,硬结,瘙痒和发热。4例治疗后有影像学好转但未达到部分缓解,40例稳定,16例进展。DTH阳性率68%(41/60)。流式细胞仪检测治疗后CD8+T细胞(CTL)明显增加(P<0.05),CD4+CD25+CD127-T细胞(Treg)降低(P<0.05)。ELISA检测IFN-γ治疗前后的变化无统计学意义,但有升高趋势。结论:异体GM-CSF联合肿瘤细胞疫苗治疗安全,耐受良好,能改善患者的机体免疫状态。Objective: To evaluate the feasibility, toxicity,immunologic,and clinical activity of tumor- Vaccination. Methods: Stage Ⅳ 60 patients by pathology were collected, including melanoma (n=11), ovary cancer (n=10), renal cell carcinoma (n=15), gastric/colorectal carcinoma (n=14), breast cancer (n-10). Vaccinations were subcutaneouly injected weekly for 6 weeks. At the first and fifth vaccine injections, DTH were injected. Lyphoma subtype and cytokine of the peripheral blood were tested at pre-, pro-treatment. Results: All the patients completed the treatment. Toxicities included local injection-site reactions, and fever. Four had mixed responses (MR), forty had stable disease (SD), sixteen had progressed disease(PD), forty-one cases had DTH positive 68% (41/60). All patients had CDS+T cell (CTL) significantly increased (P〈0.05), CD4^+CD25^+ CD 127-T cell (Treg) significantly decreased (P〈0.05). All the patients had IFN-γ increase tendency. Conclusion: This allogeneic cancer immunotherapy has a favorable safety profiles and immunologically active.
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