Modified HER-2 Tumor Antigens for Vaccination in Cancer

用于癌症疫苗接种的修饰 HER-2 肿瘤抗原

基本信息

  • 批准号:
    7288356
  • 负责人:
  • 金额:
    $ 57.48万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2004
  • 资助国家:
    美国
  • 起止时间:
    2004-03-01 至 2010-08-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (provided by applicant): Breast cancer remains 1 of the most insidious and difficult to treat human malignancies, affecting thousands of individuals each year. Our proposed studies are aimed at developing a novel tumor immunotherapy by using cryptic peptides of Her-2 protein and modified Her-2 peptides, both of which break immune tolerance to "self " tumor antigens expressed on breast cancer cells. In general, most tumor antigens have been characterized as normal, non-mutated self peptides, linking the concepts of autoimmunity with the development of tumor immunity. Our phase I studies have demonstrated the ability of peptide vaccination to elicit anti-Her-2 antibodies that resemble Herceptin, a monoclonal antibody currently approved for immunotherapy of human breast cancer. Similar to Her-2 binding by Herceptin, antibodies induced by peptide vaccination bind native Her-2 protein on living tumor cells and in solid phase immunoassays, as well as denatured Her-2 protein and peptides therein. We have demonstrated that immunization with Her-2 peptides elicits antibodies that inhibit tumor cell growth in vitro and in vivo. The goal of the Phase II study is to develop enhanced anti-Her-2 tumor immunity with a select group of Her-2 peptides in combination with adjuvants approved for human use, alum and novel TLR-based adjuvants. At present, antibody-mediated treatment of breast cancer requires prolonged administration of the therapeutic. This work will attempt to establish vaccine- based long term immunity with antibody specificities and biologic efficacy comparable to Herceptin therapy. The overall objective of this research is to develop peptide-based vaccination strategies to mimic the anti-tumor properties of Herceptin, an antibody with proven clinical efficacy in patients with breast cancer.
描述(由申请人提供):乳腺癌仍然是最隐蔽和最难治疗的人类恶性肿瘤之一,每年影响成千上万的人。我们的研究旨在开发一种新的肿瘤免疫疗法,利用Her-2蛋白的隐肽和修饰的Her-2肽,这两种肽都能打破对乳腺癌细胞上表达的“自我”肿瘤抗原的免疫耐受。一般来说,大多数肿瘤抗原的特征是正常的,非突变的自身肽,将自身免疫的概念与肿瘤免疫的发展联系起来。我们的I期研究已经证明,肽疫苗接种能够引发类似赫赛汀的抗her -2抗体,赫赛汀是一种目前被批准用于人类乳腺癌免疫治疗的单克隆抗体。与Herceptin结合Her-2类似,肽疫苗诱导的抗体将天然Her-2蛋白结合在活肿瘤细胞和固相免疫测定中,以及变性Her-2蛋白和其中的肽。我们已经证明,Her-2肽免疫可在体外和体内诱导抑制肿瘤细胞生长的抗体。II期研究的目标是通过筛选Her-2多肽与经批准的人用佐剂、明矾和新型tlr佐剂联合,开发增强的抗Her-2肿瘤免疫。目前,抗体介导的乳腺癌治疗需要延长治疗时间。这项工作将试图建立基于疫苗的长期免疫,具有抗体特异性和可与赫赛汀治疗相媲美的生物功效。这项研究的总体目标是开发基于肽的疫苗接种策略,以模仿赫赛汀的抗肿瘤特性,赫赛汀是一种已被证实对乳腺癌患者有临床疗效的抗体。

项目成果

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Mark J Mamula其他文献

Mark J Mamula的其他文献

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{{ truncateString('Mark J Mamula', 18)}}的其他基金

Multiplexed Bioassay for Checkpoint Inhibitor Autoimmunity
检查点抑制剂自身免疫的多重生物测定
  • 批准号:
    9909591
  • 财政年份:
    2019
  • 资助金额:
    $ 57.48万
  • 项目类别:
EGFR Peptides as Vaccines in Anti-Tumor Immunity
EGFR 肽作为抗肿瘤免疫疫苗
  • 批准号:
    8647974
  • 财政年份:
    2013
  • 资助金额:
    $ 57.48万
  • 项目类别:
In Vito Imaging
活体成像
  • 批准号:
    7673607
  • 财政年份:
    2008
  • 资助金额:
    $ 57.48万
  • 项目类别:
Mechanisms of Antigen Trafficking in Autoimmunity
自身免疫中抗原贩运的机制
  • 批准号:
    7680476
  • 财政年份:
    2008
  • 资助金额:
    $ 57.48万
  • 项目类别:
EGFR Peptides as Vaccines in Anti-Tumor Immunity
EGFR 肽作为抗肿瘤免疫疫苗
  • 批准号:
    8150350
  • 财政年份:
    2007
  • 资助金额:
    $ 57.48万
  • 项目类别:
EGFR Peptides as Vaccines in Anti-Tumor Immunity
EGFR 肽作为抗肿瘤免疫疫苗
  • 批准号:
    7330500
  • 财政年份:
    2007
  • 资助金额:
    $ 57.48万
  • 项目类别:
Mechanisms of Antigen Trafficking in Autoimmunity
自身免疫中抗原贩运的机制
  • 批准号:
    7352535
  • 财政年份:
    2007
  • 资助金额:
    $ 57.48万
  • 项目类别:
In Vito Imaging
活体成像
  • 批准号:
    7352530
  • 财政年份:
    2007
  • 资助金额:
    $ 57.48万
  • 项目类别:
EGFR Peptides as Vaccines in Anti-Tumor Immunity
EGFR 肽作为抗肿瘤免疫疫苗
  • 批准号:
    8000852
  • 财政年份:
    2007
  • 资助金额:
    $ 57.48万
  • 项目类别:
Modified HER-2 Tumor Antigens for Vaccination in Cancer
用于癌症疫苗接种的修饰 HER-2 肿瘤抗原
  • 批准号:
    6742316
  • 财政年份:
    2004
  • 资助金额:
    $ 57.48万
  • 项目类别:

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