Duke Brain Tumor Immunotherapy Program, Division of Neurosurgery, Department of Surgery, Duke University Medical Center, Durham, NC; Department of Biomedical Engineering, Duke University, Durham, NC; The Preston Robert Tisch Brain Tumor Center, Duke University Medical Center, Durham, NC.
Duke Brain Tumor Immunotherapy Program, Division of Neurosurgery, Department of Surgery, Duke University Medical Center, Durham, NC; Department of Biomedical Engineering, Duke University, Durham, NC; The Preston Robert Tisch Brain Tumor Center, Duke University Medical Center, Durham, NC.
Semin Oncol. 2014 Aug;41(4):496-510. doi: 10.1053/j.seminoncol.2014.06.004. Epub 2014 Jun 12.
Conventional therapy for malignant glioma (MG) fails to specifically eliminate tumor cells, resulting in toxicity that limits therapeutic efficacy. In contrast, antibody-based immunotherapy uses the immune system to eliminate tumor cells with exquisite specificity. Increased understanding of the pathobiology of MG and the profound immunosuppression present among patients with MG has revealed several biologic targets amenable to antibody-based immunotherapy. Novel antibody engineering techniques allow for the production of fully human antibodies or antibody fragments with vastly reduced antigen-binding dissociation constants, increasing safety when used clinically as therapeutics. In this report, we summarize the use of antibody-based immunotherapy for MG. Approaches currently under investigation include the use of antibodies or antibody fragments to: (1) redirect immune effector cells to target tumor mutations, (2) inhibit immunosuppressive signals and thereby stimulate an immunological response against tumor cells, and (3) provide costimulatory signals to evoke immunologic targeting of tumor cells. These approaches demonstrate highly compelling safety and efficacy for the treatment of MG, providing a viable adjunct to current standard-of-care therapy for MG.
常规的恶性神经胶质瘤 (MG) 疗法无法特异性地消除肿瘤细胞,导致毒性限制了治疗效果。相比之下,基于抗体的免疫疗法利用免疫系统以极高的特异性来消除肿瘤细胞。对 MG 的病理生物学的深入了解以及 MG 患者中存在的严重免疫抑制揭示了几种可通过基于抗体的免疫疗法来靶向的生物标志物。新型抗体工程技术可产生完全人源化抗体或抗体片段,其抗原结合解离常数大大降低,在临床上用作治疗药物时提高了安全性。在本报告中,我们总结了基于抗体的免疫疗法在 MG 中的应用。目前正在研究的方法包括使用抗体或抗体片段来:(1) 将免疫效应细胞重定向至靶向肿瘤突变,(2) 抑制免疫抑制信号,从而刺激针对肿瘤细胞的免疫反应,和 (3) 提供共刺激信号以引发针对肿瘤细胞的免疫靶向。这些方法在治疗 MG 方面显示出高度令人信服的安全性和疗效,为当前 MG 的标准治疗提供了可行的辅助手段。