期刊文献+

Ii-Key/前列腺特异性抗原CD4^+T细胞表位肽融合疫苗的制备及对PBMC的增殖影响的实验研究

Ii-Key/prostate specific antigen CD4^+T cell epitope peptide hybrid vaccine induce anti-prostate cancer immunoresponse in vitro
下载PDF
导出
摘要 目的预测并鉴定前列腺癌特异性抗原CD4+T细胞表位,并构建Ii-Key/前列腺癌特异性抗原CD4+T细胞表位肽(IiKey/PSA)疫苗的抗肿瘤效应。方法采用syfpeithi表位预测软件进行表位预测,采用酶联免疫斑点检测、淋巴细胞增殖实验对表位活化淋巴细胞的能力进行检测。结果我们预测的5条表位肽中PSA154是前列腺特异性抗原CD4+T细胞的优势表位,Ii-Key/PSA154疫苗诱导淋巴细胞活化的能力强于PSA154表位肽。结论 Ii-Key/PSA154在体外实验中显示了较强的免疫效应,可作为多肽疫苗用于表达前列腺癌特异性抗原的前列腺癌的免疫治疗。 This study was designed to predict and identify prostate cancer-specific antigen CD4+T cell epitopes for building Ii-Key/prostate cancer specific antigen CD4+T cell epitope peptides(Ii-Key/PSA),and to evaluate the anti-tumor effect of the vaccine in vitro.Syfpeithi epitope prediction software was employed to predict the epitope,while ELISPOT assay and lymphocyte proliferation assay were used to determine the ability of epitope to activate lymphocytes.Results showed that total of 5 epitopes were predicted,in which PSA154 is a superior epitope.And Ii-Key/PSA154 vaccine could induce stronger immunoresponses than PSA154 epitope peptide did.In conclusion,Ii-Key/PSA154 could use as a vaccine for prostate cancer immunotherapy.
作者 何建川 邵阳
出处 《免疫学杂志》 CAS CSCD 北大核心 2013年第10期859-862,共4页 Immunological Journal
关键词 前列腺癌特异性抗原 抗原表位 T淋巴细胞 肿瘤免疫治疗 Prostate cancer-specific antigen Epitope T lymphocyte Tumor immunotherapy
  • 相关文献

参考文献5

二级参考文献83

  • 1支轶,吴玉章,万瑛,邹丽云,郭晟,刘娜.癌胚抗原低亲和力表位改造中的分子对接[J].免疫学杂志,2005,21(6):514-517. 被引量:2
  • 2崔志刚,宋波,张立新,路浩军,李春海.MUC1黏蛋白模拟表位的筛选和鉴定[J].免疫学杂志,2006,22(2):210-212. 被引量:5
  • 3崔志刚,宋波,张立新,路浩军,李春海.稳定表达人MUC1小鼠膀胱癌细胞株和荷瘤鼠模型的建立[J].中国比较医学杂志,2006,16(7):390-393. 被引量:1
  • 4BRONTE V,MOCELLIN S.Suppressive influences in the immune response to cancer[J].J Immunother,2009,32(1):1-11. 被引量:1
  • 5YANG L,PANG Y,MOSES H-L.TGF-b and immune cells:an important regulatory axis in the tumor microenvironment and progression[J].Trends Immunol,2010,31(6):220-227. 被引量:1
  • 6NOMURA T,SAKAGUCHI S.Naturally arising CD25+CD4+ regulatory T cells in tumor immunity[J].Curr Top Microbiol Immunol,2005,293:287-302. 被引量:1
  • 7CHALMIN F,LADOIRE S,MIGNOT G,et al.Membrane-associated Hsp72 from tumor-derived exosomes mediates STAT3-dependent immunosup-pressive function of mouse and human myeloid-derived suppressor cells[J].J Clin Invest,2010,120(2):457-471. 被引量:1
  • 8LIU Z,KIM J H,FALO L D,Jr,et al.Tumor regulatory T cells potently abrogate antitumor immunity[J].J Immunol,2009,182(10):6160-6167. 被引量:1
  • 9WYSOCKI P J,KAZIMIERCZAK U,SUCHORSKA W,et al.Gene-modified tumor vaccine secreting a designer cytokine Hyper-Interleukin-6 is an effective therapy in mice bearing orthotopic renal cell cancer[J].Cancer Gene Ther,2010,17(7):465-475. 被引量:1
  • 10ANTONIA S J,SEIGNE J,DIAZ J,et al.Phase I trial of a B7-1 (CD80) gene modified autologous tumor cell vaccine in combination with systemic interleukin-2 in patients with metastatic renal cell carcinoma[J].J Urol,2002,167(5):1995-2000. 被引量:1

共引文献33

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部