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

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作者
Flavia Chiuppesi
Marcela d’Alincourt Salazar
Heidi Contreras
Vu H. Nguyen
Joy Martinez
Yoonsuh Park
Jenny Nguyen
Mindy Kha
Angelina Iniguez
Qiao Zhou
Teodora Kaltcheva
Roman Levytskyy
Nancy D. Ebelt
Tae Hyuk Kang
Xiwei Wu
Thomas F. Rogers
Edwin R. Manuel
Yuriy Shostak
Don J. Diamond
Felix Wussow
机构
[1] City of Hope National Medical Center,Department of Hematology and Transplant Center
[2] Beckman Research Institute of the City of Hope,Department of Immuno
[3] Integrative Genomics Core,Oncology
[4] Beckman Research Institute of the City of Hope,Division of Infectious Diseases and Global Public Health
[5] University of California San Diego,undefined
[6] School of Medicine,undefined
[7] Scripps Research,undefined
[8] Department of Immunology and Microbiology,undefined
[9] Research Business Development,undefined
[10] City of Hope,undefined
来源
Nature Communications | / 11卷
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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.
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