Severe Acute Respiratory Syndrome Coronavirus-2 Spike Protein Nanogel as a Pro-Antigen Strategy with Enhanced Protective Immune Responses.
Long ChenBo LiuPeng SunWenjun WangShiqiang LuoWenyuan ZhangYuanfan YangZihao WangJian LinPeng R ChenPublished in: Small (Weinheim an der Bergstrasse, Germany) (2020)
Prevention and intervention methods are urgently needed to curb the global pandemic of coronavirus disease-19 caused by severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). Herein, a general pro-antigen strategy for subunit vaccine development based on the reversibly formulated receptor binding domain of SARS-CoV-2 spike protein (S-RBD) is reported. Since the poor lymph node targeting and uptake of S-RBD by antigen-presenting cells prevent effective immune responses, S-RBD protein is formulated into a reversible nanogel (S-RBD-NG), which serves as a pro-antigen with enhanced lymph node targeting and dendritic cell and macrophage accumulation. Synchronized release of S-RBD monomers from the internalized S-RBD-NG pro-antigen triggers more potent immune responses in vivo. In addition, by optimizing the adjuvant used, the potency of S-RBD-NG is further improved, which may provide a generally applicable, safer, and more effective strategy for subunit vaccine development against SARS-CoV-2 as well as other viruses.
Keyphrases
- respiratory syndrome coronavirus
- sars cov
- coronavirus disease
- immune response
- lymph node
- dendritic cells
- anti inflammatory
- binding protein
- randomized controlled trial
- protein protein
- induced apoptosis
- cancer therapy
- early stage
- neoadjuvant chemotherapy
- toll like receptor
- amino acid
- squamous cell carcinoma
- cell cycle arrest
- case report
- transcription factor
- radiation therapy
- rectal cancer
- dna binding