Shalash Ahmed O, Azuar Armira, Madge Harrison Y R, Modhiran Naphak, Amarilla Alberto A, Liang Benjamin, Khromykh Alexander A, Hussein Waleed M, Chappell Keith J, Watterson Daniel, Young Paul R, Skwarczynski Mariusz, Toth Istvan
School of Chemistry and Molecular Biosciences, The University of Queensland, St Lucia, QLD 4072, Australia.
Australian Institute for Bioengineering and Nanotechnology, The University of Queensland, St Lucia, QLD 4072, Australia.
Pharmaceutics. 2022 Apr 13;14(4):856. doi: 10.3390/pharmaceutics14040856.
The SARS-CoV-2 virus has caused a global crisis, resulting in 0.5 billion infections and over 6 million deaths as of March 2022. Fortunately, infection and hospitalization rates were curbed due to the rollout of DNA and mRNA vaccines. However, the efficacy of these vaccines significantly drops a few months post immunization, from 88% down to 47% in the case of the Pfizer BNT162 vaccine. The emergence of variant strains, especially delta and omicron, have also significantly reduced vaccine efficacy. We propose peptide vaccines as a potential solution to address the inadequacies of the current vaccines. Peptide vaccines can be easily modified to target emerging strains, have greater stability, and do not require cold-chain storage. We screened five peptide fragments (B1-B5) derived from the SARS-CoV-2 spike protein to identify neutralizing B-cell peptide antigens. We then investigated adjuvant systems for efficient stimulation of immune responses against the most promising peptide antigens, including liposomal formulations of polyleucine (L10) and polymethylacrylate (PMA), as well as classical adjuvants (CFA and MF59). Immune efficacy of formulations was evaluated using competitive ELISA, pseudovirion neutralization, and live virus neutralization assays. Unfortunately, peptide conjugation to L10 and PMA dramatically altered the secondary structure, resulting in low antibody neutralization efficacy. Of the peptides tested, only B3 administered with CFA or MF59 was highly immunogenic. Thus, a peptide vaccine relying on B3 may provide an attractive alternative to currently marketed vaccines.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病毒引发了一场全球危机,截至2022年3月,已导致5亿人感染,600多万人死亡。幸运的是,由于DNA疫苗和信使核糖核酸(mRNA)疫苗的推出,感染率和住院率得到了控制。然而,这些疫苗的效力在免疫几个月后显著下降,以辉瑞BNT162疫苗为例,从88%降至47%。变异毒株的出现,尤其是德尔塔和奥密克戎毒株,也显著降低了疫苗效力。我们提出肽疫苗作为解决当前疫苗不足之处的潜在方案。肽疫苗可以很容易地进行改造以靶向新出现的毒株,具有更高的稳定性,并且不需要冷链储存。我们筛选了源自SARS-CoV-2刺突蛋白的五个肽片段(B1-B5),以鉴定具有中和作用的B细胞肽抗原。然后,我们研究了用于有效刺激针对最有前景的肽抗原的免疫反应的佐剂系统,包括聚亮氨酸(L10)和聚丙烯酸甲酯(PMA)的脂质体制剂,以及传统佐剂(弗氏完全佐剂和MF59)。使用竞争性酶联免疫吸附测定(ELISA)、假病毒中和试验和活病毒中和试验评估制剂的免疫效力。不幸的是,肽与L10和PMA的偶联显著改变了二级结构,导致抗体中和效力较低。在所测试的肽中,只有与弗氏完全佐剂或MF59一起使用的B3具有高度免疫原性。因此,依赖B3的肽疫苗可能为目前市场上的疫苗提供有吸引力的替代方案。