Tohumeken Sehmus, Gunduz Nuray, Demircan M Burak, Gunay Gokhan, Topal Ahmet E, Khalily M Aref, Tekinay Turgay, Dana Aykutlu, Guler Mustafa O, Tekinay Ayse B
Institute of Materials Science and Nanotechnology, National Nanotechnology Research Center (UNAM), Bilkent University, Ankara, 06800, Turkey.
Neuroscience Graduate Program, Bilkent University, Ankara, 06800, Turkey.
Adv Biosyst. 2017 May;1(5):e1700015. doi: 10.1002/adbi.201700015. Epub 2017 May 2.
The design and development of vaccines, which can induce cellular immunity, particularly CD8+ T cells hold great importance since these cells play crucial roles against cancers and viral infections. Covalent conjugation of antigen and adjuvant molecules has been used for successful promotion of immunogenicity in subunit vaccines; however, the stimulation of the CD8+ T-cell responses by this approach has so far been limited. This study demonstrates a modular system based on noncovalent attachment of biotinylated antigen to a hybrid nanofiber system consisting of biotinylated self-assembling peptide and CpG oligodeoxynucleotides (ODN) molecules, via biotin-streptavidin interaction. These peptide/oligonucleotide hybrid nanosystems are capable of bypassing prior limitations related with inactivated or live-attenuated virus vaccines and achieve exceptionally high CD8+ T-cell responses. The nanostructures are found to trigger strong IgG response and effectively modulate cross-presentation of their antigen "cargo" through close proximity between the antigen and peptide/ODN adjuvant system. In addition, the biotinylated peptide nanofiber system is able to enhance antigen uptake and induce the maturation of antigen-presenting cells. Due to its versatility, biocompatibility, and biodegradability with a broad variety of streptavidin-linked antigens, the nanosystem shown here can be utilized as an efficient strategy for new vaccine development.
能够诱导细胞免疫,特别是CD8 + T细胞的疫苗的设计和开发非常重要,因为这些细胞在对抗癌症和病毒感染中起着关键作用。抗原和佐剂分子的共价缀合已被用于成功促进亚单位疫苗的免疫原性;然而,迄今为止,这种方法对CD8 + T细胞反应的刺激作用有限。本研究展示了一种模块化系统,该系统基于生物素化抗原通过生物素-链霉亲和素相互作用非共价连接到由生物素化自组装肽和CpG寡脱氧核苷酸(ODN)分子组成的混合纳米纤维系统上。这些肽/寡核苷酸混合纳米系统能够克服与灭活或减毒活病毒疫苗相关的先前限制,并实现异常高的CD8 + T细胞反应。发现这些纳米结构能引发强烈的IgG反应,并通过抗原与肽/ODN佐剂系统之间的紧密接近有效地调节其抗原“货物”的交叉呈递。此外,生物素化肽纳米纤维系统能够增强抗原摄取并诱导抗原呈递细胞的成熟。由于其通用性、生物相容性以及与多种链霉亲和素连接抗原的生物可降解性,本文展示的纳米系统可作为新疫苗开发的有效策略。