Department of Biochemical Science and Technology, College of Life Science, National Taiwan University, Taipei, 106, Taiwan.
Department of Clinical Laboratory Sciences and Medical Biotechnology, College of Medicine, National Taiwan University, Taipei, 106, Taiwan.
Appl Microbiol Biotechnol. 2023 May;107(9):2983-2995. doi: 10.1007/s00253-023-12490-8. Epub 2023 Mar 29.
Vaccination is considered to be the most effective countermeasure to prevent and combat the global health threats of COVID-19. People with obesity are at a greater risk of hospitalization, life-threatening illness, and adverse outcomes after having COVID-19. Therefore, a safe and effective COVID-19 vaccine for obese individuals is urgently needed. In the study, the vaccine composed of the ISA 51 adjuvant and the SARS-CoV-2 spike (S) receptor-binding domain (RBD) in conjugation with the human IgG1 Fc fragment (named as ISA 51-adjuvanted RBD-Fc vaccine) was developed and inoculated in the regular chow diet (RCD) lean mice and the high-fat diet (HFD)-induced obese mice. The S protein-specific IgG titers were largely induced in an increasing manner along with three doses of ISA 51-adjuvanted RBD-Fc vaccine without causing any harmful side effect. In the HFD mice, the S protein-specific IgG titers can be quickly observed 2 weeks post the first inoculation. The antisera elicited by the ISA 51-adjuvanted RBD-Fc vaccine in the RCD and HFD mice exhibited potent SARS-CoV-2 neutralizing activities in the plaque reduction neutralization test (PRNT) assays and showed similar specificity for recognizing the key residues in the RBD which were involved in interacting with angiotensin-converting enzyme 2 (ACE2) receptor. The immune efficacy of the ISA 51-adjuvanted RBD-Fc vaccine in the HFD mice can be sustainably maintained with the PRNT50 values of 1.80-1.91×10 for at least 8 weeks post the third inoculation. Collectively, the RBD-Fc-based immunogen and the ISA 51-adjuvanted formulation can be developed as an effective COVID-19 vaccine for obese individuals. KEY POINTS: • The ISA 51-adjuvanted RBD-Fc vaccine can induce potent SARS-CoV-2 neutralizing antibodies in the obese mouse • The antibodies elicited by the ISA 51-adjuvanted RBD-Fc vaccine can bind to the key RBD residues involved in interacting with ACE2 • The immune efficacy of the ISA 51-adjuvanted RBD-Fc vaccine can be sustainably maintained for at least 8 weeks post the third inoculation.
接种疫苗被认为是预防和应对 COVID-19 这一全球健康威胁的最有效措施。肥胖人群在感染 COVID-19 后住院、出现危及生命的疾病和不良后果的风险更高。因此,迫切需要为肥胖人群开发一种安全有效的 COVID-19 疫苗。在这项研究中,开发了一种由 ISA 51 佐剂和 SARS-CoV-2 刺突(S)受体结合域(RBD)与人类 IgG1 Fc 片段缀合而成的疫苗(命名为 ISA 51 佐剂化 RBD-Fc 疫苗),并在常规饮食(RCD)瘦鼠和高脂肪饮食(HFD)诱导肥胖鼠中进行了接种。随着三剂 ISA 51 佐剂化 RBD-Fc 疫苗的接种,S 蛋白特异性 IgG 滴度呈递增趋势,且无任何有害副作用。在 HFD 小鼠中,在首次接种后 2 周即可快速观察到 S 蛋白特异性 IgG 滴度。ISA 51 佐剂化 RBD-Fc 疫苗在 RCD 和 HFD 小鼠中诱导的抗血清在蚀斑减少中和试验(PRNT)中表现出强大的 SARS-CoV-2 中和活性,并显示出对与血管紧张素转换酶 2(ACE2)受体相互作用的 RBD 关键残基的相似识别特异性。ISA 51 佐剂化 RBD-Fc 疫苗在 HFD 小鼠中的免疫效力至少可在第三次接种后 8 周内持续维持,PRNT50 值为 1.80-1.91×10。总的来说,基于 RBD-Fc 的免疫原和 ISA 51 佐剂配方可开发为肥胖人群的有效 COVID-19 疫苗。 关键点: • ISA 51 佐剂化 RBD-Fc 疫苗可在肥胖小鼠中诱导出强大的 SARS-CoV-2 中和抗体 • ISA 51 佐剂化 RBD-Fc 疫苗诱导的抗体可与 ACE2 相互作用的 RBD 关键残基结合 • ISA 51 佐剂化 RBD-Fc 疫苗的免疫效力至少可在第三次接种后 8 周内持续维持。