Development of a multi-antigenic SARS-CoV-2 vaccine candidate using a synthetic poxvirus platform

被引:65
|
作者
Chiuppesi, Flavia [1 ,2 ]
Salazar, Marcela d'Alincourt [1 ,2 ]
Contreras, Heidi [1 ,2 ]
Nguyen, Vu H. [1 ,2 ]
Martinez, Joy [1 ,2 ]
Park, Yoonsuh [1 ,2 ]
Nguyen, Jenny [1 ,2 ]
Kha, Mindy [1 ,2 ]
Iniguez, Angelina [1 ,2 ]
Zhou, Qiao [1 ,2 ]
Kaltcheva, Teodora [1 ,2 ]
Levytskyy, Roman [1 ,2 ]
Ebelt, Nancy D. [3 ]
Kang, Tae Hyuk [4 ]
Wu, Xiwei [4 ]
Rogers, Thomas F. [5 ,6 ]
Manuel, Edwin R. [3 ]
Shostak, Yuriy [7 ]
Diamond, Don J. [1 ,2 ]
Wussow, Felix [1 ,2 ]
机构
[1] City Hope Natl Med Ctr, Dept Hematol, Duarte, CA 91010 USA
[2] City Hope Natl Med Ctr, Transplant Ctr, Duarte, CA 91010 USA
[3] City Hope Natl Med Ctr, Dept Immunooncol, Beckman Res Inst, Duarte, CA 91010 USA
[4] City Hope Natl Med Ctr, Integrat Genom Core, Beckman Res Inst, Duarte, CA 91010 USA
[5] Univ Calif San Diego, Sch Med, Div Infect Dis & Global Publ Hlth, 9500 Gilman Dr, La Jolla, CA 92093 USA
[6] Scripps Res, Dept Immunol & Microbiol, 10550N Torrey Pines Rd, La Jolla, CA 92037 USA
[7] City Hope Natl Med Ctr, Res Business Dev, Duarte, CA 91010 USA
基金
美国国家卫生研究院;
关键词
VIRUS ANKARA; MOLECULAR-CLONING; GENOMIC SEQUENCE; STRAIN; DNA;
D O I
10.1038/s41467-020-19819-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Modified Vaccinia Ankara (MVA) is a highly attenuated poxvirus vector that is widely used to develop vaccines for infectious diseases and cancer. We demonstrate the construction of a vaccine platform based on a unique three-plasmid system to efficiently generate recombinant MVA vectors from chemically synthesized DNA. In response to the ongoing global pandemic caused by SARS coronavirus-2 (SARS-CoV-2), we use this vaccine platform to rapidly produce fully synthetic MVA (sMVA) vectors co-expressing SARS-CoV-2 spike and nucleocapsid antigens, two immunodominant antigens implicated in protective immunity. We show that mice immunized with these sMVA vectors develop robust SARS-CoV-2 antigen-specific humoral and cellular immune responses, including potent neutralizing antibodies. These results demonstrate the potential of a vaccine platform based on synthetic DNA to efficiently generate recombinant MVA vectors and to rapidly develop a multi-antigenic poxvirus-based SARS-CoV-2 vaccine candidate.
引用
收藏
页数:16
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