Institute of Biotechnology, National Tsing Hua University, Hsinchu, 30013, Taiwan.
Genomics Research Center, Academia Sinica, Taipei, 11529, Taiwan.
Antiviral Res. 2017 Oct;146:213-220. doi: 10.1016/j.antiviral.2017.09.014. Epub 2017 Sep 22.
Humans infected with H7N9 avian influenza viruses can result in severe pneumonia and acute respiratory syndrome with an approximately 40% mortality rate, and there is an urgent need to develop an effective vaccine to reduce its pandemic potential. In this study, we used a novel PELC/CpG adjuvant for recombinant H7HA (rH7HA) subunit vaccine development. After immunizing BALB/c mice intramuscularly, rH7HA proteins formulated in this adjuvant instead of an alum adjuvant elicited higher IgG, hemagglutination-inhibition, and virus neutralizing antibodies in sera; induced higher numbers of H7HA-specific IFN-γ-secreting T cells and antibody secreting cells in spleen; and provided improved protection against live virus challenges. Our results indicate that rH7HA proteins formulated in PELC/CpG adjuvant can induce potent anti-H7N9 immunity that may provide useful information for H7N9 subunit vaccine development.
人感染 H7N9 禽流感病毒可导致严重肺炎和急性呼吸窘迫综合征,死亡率约为 40%,因此迫切需要开发有效的疫苗来降低其大流行的潜力。在这项研究中,我们使用了一种新型的 PELC/CpG 佐剂来开发重组 H7HA(rH7HA)亚单位疫苗。通过肌肉内免疫 BALB/c 小鼠,用这种佐剂配制的 rH7HA 蛋白而不是明矾佐剂在血清中引发了更高水平的 IgG、血凝抑制和病毒中和抗体;诱导了更多的 H7HA 特异性 IFN-γ 分泌 T 细胞和抗体分泌细胞在脾脏中;并提供了针对活病毒攻击的更好保护。我们的结果表明,用 PELC/CpG 佐剂配制的 rH7HA 蛋白可以诱导有效的抗 H7N9 免疫,这可能为 H7N9 亚单位疫苗的开发提供有用的信息。