Breaking tolerance to mEGP self-antigen

打破对 mEGP 自身抗原的耐受性

• 批准号: 7030572
• 负责人: DOROTHEE M HERLYN
• 金额: $ 22.62万
• 依托单位: WISTAR INSTITUTE
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-01-01 至 2009-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7030572
• 关键词: antibody; autoantigens; carcinoma; immunotherapy; model; neoplasm /cancer; peptides

DESCRIPTION (provided by applicant): Most tumor antigens (Ag) are also expressed by normal tissues and therefore induce immunological tolerance in the tumor-bearing host. Yet, these self proteins are major targets available for active specific immunotherapies. These therapies need to be developed in animal models that mimic the conditions in cancer patients. The human gastrointestinal carcinoma-associated Ag GA733 (EpCAM) has been a suitable target for passive and active immunotherapy of these tumors in cancer patients. Mice expressing the homologue of the human Ag, murine epithelial glycoprotein (mEGP), on normal and tumor tissues provide a relevant animal model of active specific immunotherapy against the GA733 Ag. Our major goal is to define vaccines that significantly and reproducibly inhibit growth of established mouse colon carcinoma cells in this tumor model system. Our major hypothesis is that mimics of mEGP, by virtue of being similar, but not identical to mEGP will effectively immunize mice and induce regression of established, mEGP-positive colon carcinomas. Specifically we will: 1) Test the hypothesis that mEGP mimics induce protective immunity against established, subcutaneous tumors and visceral metastasis. This involves: a) Generation and selection of mEGP mimics (anti-idiotypic antibodies [Ab2], Ab2 fragments, peptides or minigenes derived from the VH and VL regions of Ab2, peptides derived from synthetic libraries and mimicking the epitope recognized by anti-mEGP monoclonal antibody, and peptides and minigenes of mEGP CTL epitopes); and b) Evaluation of vaccines for their capacity to inhibit subcutaneous and visceral, metastatic growth of CT26-mEGP colon carcinoma cells in the therapeutic setting in mice. 2) Determine the mechanism of tumor growth inhibition by mEGP mimics. This involves: a) Evaluation of humoral immune responses (cytotoxic antibodies) and cellular immune responses (proliferative, cytotoxic and delayed-type hypersensitive lymphocytes in mice with regressing tumors after immunization with mEGP mimics; b) Determination of the direct role in tumor growth inhibition of antibodies, CD8+ or CD4+ T lymphocytes, memory lymphocytes, and epitope spreading. The proposed studies provide the basis for vaccinations of colorectal cancer patients against the GA733 Ag.

描述(申请人提供)：大多数肿瘤抗原(Ag)也在正常组织中表达，因此在荷瘤宿主中诱导免疫耐受。然而，这些自身蛋白是主动特异性免疫疗法的主要靶点。这些疗法需要在动物模型中开发，以模拟癌症患者的情况。人胃肠道肿瘤相关抗原GA733(EpCAM)已成为肿瘤患者被动和主动免疫治疗的理想靶点。在正常组织和肿瘤组织上表达人抗原同源物--小鼠上皮糖蛋白(MEGP)的小鼠，为针对GA733抗原的主动特异性免疫治疗提供了相关的动物模型。我们的主要目标是定义在这个肿瘤模型系统中显著且可重复地抑制已建立的小鼠结肠癌细胞生长的疫苗。我们的主要假设是，由于与mEGP相似但不完全相同，mEGP的模拟物将有效地免疫小鼠，并诱导已建立的mEGP阳性结肠癌的消退。具体地说，我们将：1)测试mEGP模拟物诱导对已建立的皮下肿瘤和内脏转移的保护性免疫的假设。这包括：a)产生和选择mEGP模拟物(来自AB2的VH和VL区域的抗独特型抗体[AB2]、AB2片段、多肽或微基因)；来自合成文库的模仿抗mEGP单抗识别表位的肽，以及mEGP CTL表位的多肽和微基因)；以及b)在治疗环境中评价疫苗抑制CT26-mEGP结肠癌细胞皮下和内脏转移生长的能力。2)确定mEGP模拟物抑制肿瘤生长的机制。这涉及：a)评估mEGP模拟物免疫后肿瘤消退小鼠的体液免疫反应(细胞毒性抗体)和细胞免疫反应(增殖、细胞毒性和迟发性超敏淋巴细胞)；b)确定抗体、CD8+或CD4+T淋巴细胞、记忆淋巴细胞和表位扩散在抑制肿瘤生长中的直接作用。本研究为结直肠癌患者接种GA733抗原疫苗奠定了基础。