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Rejection of Tumors by MHC Class Ib-Restricted CTL

Rejection of Tumors by MHC Class Ib-Restricted CTL
MHC Ib 类限制性 CTL 对肿瘤的排斥
批准号:
6836678
负责人:
EUGENE Y CHIANG
金额:
$4.3万
依托单位国家:
美国
项目类别:
财政年份:
2004
资助国家:
美国
项目状态:
已结题
起止时间:
2004-09-01 至 2007-08-31

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中文摘要
翻译
描述(由申请人提供):Q9是一种小鼠非多态性非经典Ib类MHC分子,在所有表达Q9的小鼠系源性肿瘤细胞系中被观察到下调或缺失。此外,已发现Q9可保护宿主动物免受黑色素瘤肿瘤的攻击。本应用的重点是确定Q9是否作为同基因肿瘤反应性ctl的限制因子。本实验旨在建立确定CTL参与Q9介导的模型肿瘤排斥反应和高效抗肿瘤CTL生成的方案,提供这些CTL的详细特征,并评估在Q9背景下出现的潜在肿瘤相关抗原。用于实现这些目标的方法将包括体外细胞毒性测定、流式细胞术分析、微阵列分析、激光捕获显微镜、实时定量PCR和蛋白质纯化。这些研究可能导致通用肽疫苗的发展,从而为癌症的治疗做出重大贡献。与Q9模型Ib类抗原的合作也将为未来研究人类I类MHC(如HLA-C和/或HLA-E, -F, -G或其他尚未发现的I类分子)奠定基础。
英文摘要
DESCRIPTION (provided by applicant): Q9, a murine non-polymorphic nonclassical class Ib MHC molecule, has been observed to be downregulated or lost in all Q9-expressing mouse strain-derived tumor cell lines. Furthermore, Q9 has been found to confer protection to host animals from melanoma tumor challenge. The focus of this application is to determine if Q9 functions as a restriction element for syngeneic tumor-reactive CTLs. The proposed experiments aim to establish protocols for the determination of CTL participation in Q9-mediated rejection of model tumors and for the generation of highly potent antitumor CTLs, to provide a detailed characterization of these CTLs, and to evaluate potential tumor-associated antigens that are presented in the context of Q9. Methods used to achieve these aims will include in vitro cytotoxicity assays, flow cytometry analyses, microarray analyses, laser capture microscopy, real-time quantitative PCR and protein purification. These studies may lead to the development of universal peptide vaccines, thereby providing a significant contribution to the treatment of cancers. Work with the Q9 model class Ib antigen will also lay a foundation for future studies with human class I MHC such as HLA-C and/or HLA-E, -F, -G or other yet undiscovered class I molecules.
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Rejection of Tumors by MHC Class Ib-Restricted CTL
  • 批准号:
    6944827
  • 项目类别:
  • 资助金额:
    $4.83万
  • 财政年份:
    2004
  • 负责人:
    EUGENE Y CHIANG
  • 依托单位: