Kawakita Tomomi, Sekiya Toshiki, Kameda Yayoi, Nomura Naoki, Ohno Marumi, Handabile Chimuka, Yamaya Akari, Fukuhara Hideo, Anraku Yuki, Kita Shunsuke, Toba Shinsuke, Tsukamoto Hirotake, Sawa Tomohiro, Oshiumi Hiroyuki, Itoh Yasushi, Maenaka Katsumi, Sato Akihiko, Sawa Hirofumi, Suzuki Yasuhiko, Brown Lorena E, Jackson David C, Kida Hiroshi, Matsumoto Misako, Seya Tsukasa, Shingai Masashi
Division of Vaccine Immunology, International Institute for Zoonosis Control, Hokkaido University, Sapporo, Japan.
Institute for Vaccine Research and Development (HU-IVReD), Hokkaido University, Sapporo, Japan.
J Virol. 2025 May 20;99(5):e0229024. doi: 10.1128/jvi.02290-24. Epub 2025 Apr 15.
UNLABELLED: ARNAX is a synthetic nucleotide-based Toll-like receptor 3 (TLR3) ligand that specifically stimulates the TLR3/TIR domain-containing adaptor molecule 1 (TICAM-1) pathway without activating inflammatory responses. ARNAX activates cellular immunity via cross-presentation; hence, its practical application has been demonstrated in cancer immunotherapy. Given the importance of cellular immunity in virus infections, ARNAX is expected to be a more effective vaccine adjuvant for virus infections than alum, an adjuvant approved for human use that mainly enhances humoral immunity. In the present study, the trimeric recombinant spike protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was prepared as a vaccine antigen and formulated with ARNAX. When T-cell and neutralizing antibody responses were evaluated in immunized mice, antigen formulated with ARNAX generated significantly larger numbers of antigenspecific CD4 and CD8 T cells, as well as higher titers of neutralizing antibodies, compared to antigen alone or antigen formulated with alum. In experiments where immunized mice were challenged with a SARS-CoV-2 mouse-adapted virus derived from the ancestral strain, immunization with antigen formulated with ARNAX reduced virus titers in the lungs at 3 days post-infection to a much greater extent than did immunization with either antigen alone or that formulated with alum. These results show that ARNAX potently enhances the levels of both cellular and humoral immunity above those seen with alum, providing significantly greater viral clearing responses. Thus, ARNAX may act as a useful adjuvant for prophylactic vaccines, particularly for viral infectious diseases. IMPORTANCE: Cellular immunity is a critical immunological defense system against virus infections. However, aluminum salts, the most widely used adjuvant for vaccines for human use, do not promote strong cellular immunity. To prepare for the next pandemic of viral origin, the development of Th1-type adjuvants with low adverse reactions that induce cellular immunity is necessary. ARNAX is a TLR3 agonist consisting of DNA-RNA hybrid nucleic acid, which is expected to be an adjuvant that induces cellular immunity. The present study using a coronavirus disease 2019 mouse model demonstrated that ARNAX potently induces cellular immunity in addition to humoral immunity with minimal induction of inflammatory cytokines. Therefore, ARNAX has the potential to be used as a potent and welltolerated adjuvant for vaccines against pandemic viruses emerging in the future.
未标记:ARNAX是一种基于合成核苷酸的Toll样受体3(TLR3)配体,可特异性刺激含TLR3/TIR结构域的衔接分子1(TICAM-1)途径,而不激活炎症反应。ARNAX通过交叉呈递激活细胞免疫;因此,其在癌症免疫治疗中的实际应用已得到证实。鉴于细胞免疫在病毒感染中的重要性,预计ARNAX作为病毒感染的疫苗佐剂比明矾更有效,明矾是一种已获批准用于人类的佐剂,主要增强体液免疫。在本研究中,制备了严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的三聚体重组刺突蛋白作为疫苗抗原,并与ARNAX配制成制剂。当在免疫小鼠中评估T细胞和中和抗体反应时,与单独的抗原或与明矾配制成制剂的抗原相比,与ARNAX配制成制剂的抗原产生了数量显著更多的抗原特异性CD4和CD8 T细胞,以及更高滴度的中和抗体。在用源自原始毒株的适应小鼠的SARS-CoV-2病毒攻击免疫小鼠的实验中,与单独使用抗原或与明矾配制成制剂的抗原免疫相比,用与ARNAX配制成制剂的抗原免疫在感染后3天更显著地降低了肺部的病毒滴度。这些结果表明,ARNAX能有力地增强细胞免疫和体液免疫水平,使其高于明矾组,提供显著更强的病毒清除反应。因此,ARNAX可能作为预防性疫苗的有用佐剂,特别是用于病毒感染性疾病。 重要性:细胞免疫是抵抗病毒感染的关键免疫防御系统。然而,铝盐是人类疫苗中使用最广泛的佐剂,却不能促进强大的细胞免疫。为应对下一次病毒起源的大流行,开发具有低不良反应且能诱导细胞免疫的Th1型佐剂是必要的。ARNAX是一种由DNA-RNA杂交核酸组成的TLR3激动剂,有望成为一种诱导细胞免疫的佐剂。本研究使用2019冠状病毒病小鼠模型表明,ARNAX除了诱导体液免疫外,还能有力地诱导细胞免疫,且诱导的炎性细胞因子最少。因此,ARNAX有潜力用作针对未来出现的大流行病毒的疫苗的有效且耐受性良好的佐剂。
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