Research and Development Center, NA Vaccine Institute, Seoul, Republic of Korea.
Interdisciplinary Program in Genetic Engineering, College of Natural Sciences, Seoul National University, Seoul, Republic of Korea.
Front Immunol. 2023 Jan 24;14:1075291. doi: 10.3389/fimmu.2023.1075291. eCollection 2023.
Synthetic double-stranded RNA analogs recognized by Toll-like receptor 3 (TLR3) are an attractive adjuvant candidate for vaccines, especially against intracellular pathogens or tumors, because of their ability to enhance T cell and antibody responses. Although poly(I:C) is a representative dsRNA with potent adjuvanticity, its clinical application has been limited due to heterogeneous molecular size, inconsistent activity, poor stability, and toxicity. To overcome these limitations, we developed a novel dsRNA-based TLR3 agonist named NexaVant (NVT) by using PCR-coupled bidirectional transcription. Agarose gel electrophoresis and reverse phase-HPLC analysis demonstrated that NVT is a single 275-kDa homogeneous molecule. NVT appears to be stable since its appearance, concentration, and molecular size were unaffected under 6 months of accelerated storage conditions. Moreover, preclinical evaluation of toxicity under good laboratory practices showed that NVT is a safe substance without any signs of serious toxicity. NVT stimulated TLR3 and increased the expression of viral nucleic acid sensors TLR3, MDA-5, and RIG-1. When intramuscularly injected into C57BL/6 mice, ovalbumin (OVA) plus NVT highly increased the migration of dendritic cells (DCs), macrophages, and neutrophils into inguinal lymph node (iLN) compared with OVA alone. In addition, NVT substantially induced the phenotypic markers of DC maturation and activation including MHC-II, CD40, CD80, and CD86 together with IFN-β production. Furthermore, NVT exhibited an appropriate adjuvanticity because it elevated OVA-specific IgG, in particular, higher levels of IgG2c (Th1-type) but lower IgG1 (Th2-type). Concomitantly, NVT increased the levels of Th1-type T cells such as IFN-γCD4 and IFN-γCD8 cells in response to OVA stimulation. Collectively, we suggest that NVT with appropriate safety and effectiveness is a novel and promising adjuvant for vaccines, especially those requiring T cell mediated immunity such as viral and cancer vaccines.
人工合成的双链 RNA 类似物被 Toll 样受体 3(TLR3)识别,是一种有吸引力的疫苗佐剂候选物,特别是针对细胞内病原体或肿瘤,因为它们能够增强 T 细胞和抗体反应。虽然聚肌苷酸(poly(I:C))是一种具有强大佐剂活性的代表性双链 RNA,但由于其分子大小不均一、活性不一致、稳定性差和毒性等问题,其临床应用受到限制。为了克服这些限制,我们通过 PCR 偶联双向转录开发了一种新型双链 RNA 型 TLR3 激动剂,命名为 NexaVant(NVT)。琼脂糖凝胶电泳和反相高效液相色谱分析表明,NVT 是一种单一的 275kDa 均一分子。NVT 似乎很稳定,因为在加速储存 6 个月的条件下,其外观、浓度和分子量均不受影响。此外,根据良好实验室规范进行的毒性临床前评估表明,NVT 是一种安全的物质,没有任何严重毒性的迹象。NVT 刺激 TLR3 并增加病毒核酸传感器 TLR3、MDA-5 和 RIG-1 的表达。当肌肉内注射到 C57BL/6 小鼠中时,与单独的 OVA 相比,卵清蛋白(OVA)加 NVT 高度增加了树突状细胞(DC)、巨噬细胞和中性粒细胞向腹股沟淋巴结(iLN)的迁移。此外,NVT 还显著诱导了 DC 成熟和激活的表型标志物,包括 MHC-II、CD40、CD80 和 CD86 以及 IFN-β 的产生。此外,NVT 表现出适当的佐剂活性,因为它提高了 OVA 特异性 IgG,特别是 IgG2c(Th1 型)的水平更高,但 IgG1(Th2 型)的水平更低。同时,NVT 增加了 IFN-γCD4 和 IFN-γCD8 等 Th1 型 T 细胞的水平,以响应 OVA 刺激。综上所述,我们认为 NVT 具有适当的安全性和有效性,是一种新型的有前途的疫苗佐剂,特别是那些需要 T 细胞介导的免疫,如病毒和癌症疫苗。