Bifunctional Immunostimulatory Antibodies for Treatment of Breast Cancer

用于治疗乳腺癌的双功能免疫刺激抗体

• 批准号: 8671472
• 负责人: ATUL BEDI
• 金额: $ 33.62万
• 依托单位: JOHNS HOPKINS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2014
• 资助国家: 美国
• 起止时间: 2014-07-11 至 2019-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8671472
• 关键词: A Mouse; Advanced Development; Antibodies; Attenuated; BALB/c Nude Mouse; Bispecific Antibodies; Boxing; Breast Cancer Treatment; CD28 gene; CD34 gene; CD4 Positive T Lymphocytes; CD8B1 gene; CTLA4 gene; Cells; Cessation of life; Cetuximab; Clinical; Cytotoxic T-Lymphocyte-Associated Protein 4; Development; ERBB2 gene; Effector Cell; Epidermal Growth Factor Receptor; Epithelial; Exhibits; Extracellular Domain; Gene Expression Profile; Genes; Growth Factor Receptors; Hematopoietic; Hormonal; Hormone Receptor; Human; Immune; Immune Tolerance; Immune response; Immune system; Immunity; Immunologic Surveillance; Immunosuppression; Immunosuppressive Agents; Immunotherapeutic agent; Infiltration; Lung; Malignant Epithelial Cell; Malignant Neoplasms; Mediating; Mesenchymal; Mus; Natural Killer Cells; Neoplasm Metastasis; Patients; Population; Production; Refractory; Regulatory T-Lymphocyte; Resistance; Risk; Role; Signal Transduction; T-Cell Activation; T-Lymphocyte; Testing; Therapeutic antibodies; Toxic effect; Transforming Growth Factors; Translations; Xenograft procedure; antibody-dependent cell cytotoxicity; comparative efficacy; cytokine; cytotoxic; design; forkhead protein; high risk; immune function; improved; in vivo; malignant breast neoplasm; neoplastic cell; novel; novel therapeutics; overexpression; public health relevance; receptor; reconstitution; response; triple-negative invasive breast carcinoma; tumor; tumor microenvironment; tumor progression

DESCRIPTION (provided by applicant): Cancers circumvent immune surveillance via production of transforming growth factor-¿ (TGF-¿), a multifunctional cytokine that facilitates tumor progression, invasion, and metastasis via promotion of epithelial- mesenchymal transition (EMT) and suppression of immune responses. TGF-¿ directly attenuates the activation and cytotoxic function of immune effector cells (NK cells and CD8+ T cells), and promotes the development and function of regulatory T cells (Tregs), a sub-population of immunosuppressive CD4+ T cells that express forkhead box P3 (FoxP3+). TGF-¿ induces expression of FoxP3, which upregulates cytotoxic T lymphocyte antigen-4 (CTLA-4), a molecule that restrains the activation of T cells. Our studies demonstrate that TGF-¿ and CTLA-4 function as cooperative, yet redundant, brakes on the immune system, and indicate that the abrogation of these immune checkpoints is required to counteract Tregs and unleash innate and adaptive immune responses against tumor cells. To advance this strategy, we have developed two novel bifunctional immunostimulatory antibodies to counteract TGF-¿ in the microenvironment of the targeted tumor cell or Treg: 1. Anti-EGFR-TGF¿RII: A bifunctional antibody that sequesters TGF-¿ via an extracellular domain sequence of TGF Receptor II fused to the C-terminus of the heavy chain of anti-EGFR antibody (Cetuximab). 2. Anti-CTLA4-TG¿RII: A bifunctional antibody that sequesters TGF-¿ via an extracellular domain sequence of TGF-¿ Receptor II fused to the C-terminus of the heavy chain of anti-CTLA-4 antibody (Ipilimumab). Approximately 15-25% of patients with breast cancer have triple negative breast cancer (TNBC), an aggressive treatment-refractory subtype that lacks hormone receptors and HER2/neu. Although 80% of TNBC overexpress epidermal growth factor receptor (EGFR), they do not respond to cetuximab. Our studies demonstrate that TGF-¿ is a key determinant of the resistance of cancers to cetuximab. Since TNBC exhibit EMT and Treg infiltration, the tell-tale signs of TGF-¿ activity, they may be ideal targets for targeted bifunctional immunostimulatory antibodies that counteract TGF-¿-mediated immune tolerance. The Specific Aims are: I. Evaluate the antitumor efficacy of anti-EGFR-TGF¿RII in TNBC tumor-bearing mice: (A) Examine whether anti-EGFR-TGF¿RII has superior antitumor efficacy compared to cetuximab, and determine the role of ADCC in its mechanism of action; (B) Examine whether anti-EGFR-TGF¿RII can reverse immune tolerance and enhance T cell-mediated tumor regression in NOG mice reconstituted with human CD34+ cells. II. Evaluate the antitumor efficacy of anti-CTLA-4-TGF¿RII in TNBC-bearing NOG mice reconstituted with human CD34+ cells: (A) Examine whether anti-CTLA-4-TGF¿RII counteracts Tregs and activates antitumor immunity; (B) Compare the antitumor efficacy of anti-CTLA-4-TGF¿RII with that of Ipilimumab or anti-TGF-¿. IMPACT: The project seeks to advance the treatment of TNBC and other common cancers by counteracting tumor-induced immune tolerance via novel targeted bifunctional immunostimulatory antibodies.

描述（由申请人提供）：癌症通过产生转化生长因子-β（TGF-β）规避免疫监视，TGF-β是一种多功能细胞因子，通过促进上皮-间质转化（EMT）和抑制免疫应答促进肿瘤进展、侵袭和转移。TGF-β直接减弱免疫效应细胞（NK细胞和CD 8 + T细胞）的活化和细胞毒性功能，并促进调节性T细胞（TCLs）的发育和功能，TCLs是表达叉头框P3（FoxP 3+）的免疫抑制性CD 4 + T细胞亚群。TGF-β诱导FoxP 3的表达，FoxP 3上调细胞毒性T淋巴细胞抗原-4（CTLA-4），这是一种抑制T细胞活化的分子。我们的研究表明，TGF-β和CTLA-4作为合作，但多余的，制动免疫系统，并表明，这些免疫检查点的废除是需要抵消TGFAP和释放先天性和适应性免疫反应对肿瘤细胞。为了推进这一策略，我们开发了两种新型的双功能免疫刺激抗体，以抵消靶向肿瘤细胞或Treg微环境中的TGF-β：1。抗EGFR-TGF？RII：一种双功能抗体，通过与抗EGFR抗体（西妥昔单抗）重链C端融合的TGF受体II细胞外结构域序列螯合TGF-β。2.抗CTLA 4-TG ³ RII：一种双功能抗体，通过融合至抗CTLA-4抗体（伊匹单抗）重链C末端的TGF-β受体II的细胞外结构域序列螯合TGF-β。大约15-25%的乳腺癌患者患有三阴性乳腺癌（TNBC），这是一种缺乏激素受体和HER 2/neu的侵袭性治疗难治性亚型。尽管80%的TNBC过表达表皮生长因子受体（EGFR），但它们对西妥昔单抗无反应。我们的研究表明，TGF-β是癌症对西妥昔单抗耐药的关键决定因素。由于TNBC表现出EMT和Treg浸润，这是TGF-β活性的标志，它们可能是靶向双功能免疫刺激抗体的理想靶点，这些抗体可以抵消TGF-β介导的免疫耐受。具体目标是：一。评价抗EGFR-TGF RII在TNBC荷瘤小鼠中的抗肿瘤功效：（A）检查抗EGFR-TGF RII是否具有比西妥昔单抗更上级的抗肿瘤功效，并确定ADCC在其作用机制中的作用;（B）检查抗EGFR-TGF RII是否可以逆转免疫耐受并增强用人CD 34+细胞重建的NOG小鼠中T细胞介导的肿瘤消退。二.在用人CD 34+细胞重建的携带TNBC的NOG小鼠中评价抗CTLA-4-TGF <$RII的抗肿瘤功效：（A）检查抗CTLA-4-TGF <$RII是否抵消TNBC并激活抗肿瘤免疫;（B）比较抗CTLA-4-TGF <$RII与伊匹单抗或抗TGF <$RII的抗肿瘤功效。影响：该项目旨在通过新型靶向双功能免疫刺激抗体对抗肿瘤诱导的免疫耐受来推进TNBC和其他常见癌症的治疗。