Litcius/Paper detail

Single-shot AAV-vectored vaccine against SARS-CoV-2 with fast and long-lasting immunity

Fuhua Wu, Shuang Luo, Yongshun Zhang, Yangsen Ou, Hairui Wang, Zhaofei Guo, Chun‐Ting He, Shuting Bai, Penghui He, M. Jiang, Xiaoyan Chen, Guangsheng Du, Xun Sun

2022Acta Pharmaceutica Sinica B28 citationsDOIOpen Access PDF

Abstract

Due to the insufficient long-term protection and significant efficacy reduction to new variants of current COVID-19 vaccines, the epidemic prevention and control are still challenging. Here, we employ a capsid and antigen structure engineering (CASE) strategy to manufacture an adeno-associated viral serotype 6-based vaccine (S663V-RBD), which expresses trimeric receptor binding domain (RBD) of spike protein fused with a biological adjuvant RS09. Impressively, the engineered S663V-RBD could rapidly induce a satisfactory RBD-specific IgG titer within 2 weeks and maintain the titer for more than 4 months. Compared to the licensed BBIBP-CorV (Sinopharm, China), a single-dose S663V-RBD induced more endurable and robust immune responses in mice and elicited superior neutralizing antibodies against three typical SARS-CoV-2 pseudoviruses including wild type, C.37 (Lambda) and B.1.617.2 (Delta). More interestingly, the intramuscular injection of S663V-RBD could overcome pre-existing immunity against the capsid. Given its effectiveness, the CASE-based S663V-RBD may provide a new solution for the current and next pandemic.

Topics & Concepts

CapsidVirologyTiterImmunityAdjuvantAntibodyNeutralizing antibodySevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)Antibody titerMedicineCoronavirus disease 2019 (COVID-19)ImmunologyAntigenBiologyImmune systemVirusDiseaseInfectious disease (medical specialty)Internal medicineSARS-CoV-2 and COVID-19 ResearchVirus-based gene therapy researchViral Infections and Immunology Research