Mouse Model for Antigen Specific Immunotherapy of Cancer

癌症抗原特异性免疫治疗的小鼠模型

• 批准号: 7229033
• 负责人: Jill E Slansky
• 金额: $ 26.94万
• 依托单位: UNIVERSITY OF COLORADO DENVER
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-07-09 至 2009-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7229033
• 关键词: Affinity; Amino Acid Substitution; Amino Acids; Antigens; Antitumor Response; Autoantigens; Baculoviruses; Binding; Biological Models; CD8B1 gene; Characteristics; Clinical; Colon Carcinoma; Complex; Immune response; Immune system; Immunity; Immunotherapy; Individual; Libraries; MHC binding peptide; Methodology; Mus; Mutate; Peptide/MHC Complex; Peptides; Positioning Attribute; Proteins; Recruitment Activity; Side; Specific qualifier value; System; T-Lymphocyte; Testing; Tumor Antigens; cancer immunotherapy; clinically relevant; design; mouse model; novel; novel therapeutics; research study; response; success; tumor; tumor growth

DESCRIPTION (provided by applicant): Boosting the T cell response for tumor-associated antigens with mimotopes, peptide mimics of antigens, is a practical clinical strategy that does not require the identification of specific antigens for individual tumors. Clinical success employing this strategy has been promising, but inconsistent. Such approaches may be enhanced by a better understanding of the parameters of peptide/MHC binding to the TCR and the optimal T cell repertoire required for effective antitumor responses. Our overall hypothesis is that mimotopes can be designed to efficiently augment the immune response to tumors. Using a mouse tumor model system, we will determine whether increased affinity of the TCR-mimotope/MHC complex correlates with increased antitumor activity. In addition, using a new system to systematically screen a library of mimotopes of a given affinity and capacity to stimulate T cell clones, we will determine other characteristics of effective mimotopes. Specifically, we will determine whether mimotopes with either altered TCR-contact residues or with the same TCR-contact residues, but altered rotomers of the amino acid side chains that contact the TCR, are more efficient in augmenting the T cell response to tumors. Finally, we will determine whether activating a more diverse TAA-specific T cell repertoire will boost antitumor immunity. These studies will contribute to the design of new therapeutic strategies that involve stimulating the immune system to tumor antigens.

描述（由申请人提供）：用模拟表位（抗原的肽模拟物）增强对肿瘤相关抗原的T细胞应答是一种实用的临床策略，不需要鉴定单个肿瘤的特异性抗原。采用这种策略的临床成功是有希望的，但不一致。这些方法可以通过更好地理解肽/MHC与TCR结合的参数和有效抗肿瘤反应所需的最佳T细胞库来增强。我们的总体假设是，模拟表位可以被设计成有效地增强对肿瘤的免疫应答。使用小鼠肿瘤模型系统，我们将确定TCR-模拟表位/MHC复合物的亲和力增加是否与抗肿瘤活性增加相关。此外，使用一种新的系统来系统地筛选具有给定亲和力和刺激T细胞克隆能力的模拟表位库，我们将确定有效模拟表位的其他特征。具体而言，我们将确定具有改变的TCR接触残基或具有相同的TCR接触残基但改变了与TCR接触的氨基酸侧链的旋转异构体的模拟表位是否在增强T细胞对肿瘤的应答中更有效。最后，我们将确定激活更多样化的TAA特异性T细胞库是否会增强抗肿瘤免疫力。这些研究将有助于设计新的治疗策略，包括刺激免疫系统的肿瘤抗原。