Severe Acute Respiratory Syndrome Coronavirus-2 Spike Protein Nanogel as a Pro-Antigen Strategy with Enhanced Protective Immune Responses

被引:13
作者
Chen, Long [1 ]
Liu, Bo [2 ]
Sun, Peng [2 ]
Wang, Wenjun [3 ]
Luo, Shiqiang [2 ,4 ]
Zhang, Wenyuan [1 ]
Yang, Yuanfan [1 ]
Wang, Zihao [5 ]
Lin, Jian [1 ]
Chen, Peng R. [1 ,6 ]
机构
[1] Peking Univ, Minist Educ, Coll Chem & Mol Engn, Beijing Natl Lab Mol Sci,Key Lab Bioorgan Chem &, Beijing 100871, Peoples R China
[2] Beijing Inst Biotechnol, Dept Microorganism Engn, Beijing 100071, Peoples R China
[3] Chinese Acad Sci, Univ Chinese Acad Sci, Coll Life Sci, Inst Biophys,Key Lab Infect & Immun, Beijing 100101, Peoples R China
[4] Anhui Univ, Inst Phys Sci & Informat, Hefei 230601, Peoples R China
[5] Beijing Inst Pharmacol & Toxicol, Beijing 100850, Peoples R China
[6] Peking Univ, Peking Tsinghua Ctr Life Sci, Beijing, Peoples R China
基金
中国国家自然科学基金;
关键词
coronavirus disease‐ 19; nanogel; receptor binding domain; severe acute respiratory syndrome coronavirus‐ 2; subunit vaccine; RECEPTOR-BINDING DOMAIN; VACCINE;
D O I
10.1002/smll.202004237
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
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页数:8
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