Santulli-Marotto Sandra, Nair Smita K, Rusconi Chris, Sullenger Bruce, Gilboa Eli
Center for Genetic and Cellular Therapies, Department of Surgery, Duke University Medical Center, Durham, North Carolina 27710, USA.
Cancer Res. 2003 Nov 1;63(21):7483-9.
The potency of cancer immunotherapy can be enhanced by administration of high-avidity ligands specific to receptors expressed on T cells. Antibodies or cytokines are the main agents used in such capacity. Antibody-mediated inhibition of cytotoxic T cell antigen-4 (CTLA-4) function in mice augments antitumor immunity and could serve as an important adjunct in cancer immunotherapy. However, antibody-based therapy used in the setting of chronic diseases such as cancer poses significant cost, manufacturing, and regulatory challenges. Here we describe the development of RNA aptamers that bind CTLA-4 with high affinity and specificity. These aptamers inhibit CTLA-4 function in vitro and enhance tumor immunity in mice. Moreover, assembly of the aptamers into tetrameric forms significantly enhances their bioactivity in vitro and in vivo. These results demonstrate that aptamers can be used to manipulate the immune system for therapeutic applications and that multivalent versions of aptamers may be particularly potent agents in vivo.
通过给予对T细胞上表达的受体具有高亲和力的配体,可以增强癌症免疫疗法的效力。抗体或细胞因子是具有这种作用的主要药物。抗体介导的对小鼠细胞毒性T细胞抗原4(CTLA-4)功能的抑制增强了抗肿瘤免疫力,并且可以作为癌症免疫疗法中的重要辅助手段。然而,用于癌症等慢性疾病的基于抗体的疗法带来了巨大的成本、生产和监管挑战。在这里,我们描述了与CTLA-4具有高亲和力和特异性结合的RNA适配体的开发。这些适配体在体外抑制CTLA-4功能,并增强小鼠的肿瘤免疫力。此外,将适配体组装成四聚体形式可显著增强其在体外和体内的生物活性。这些结果表明,适配体可用于操纵免疫系统以用于治疗应用,并且适配体的多价形式在体内可能是特别有效的药物。