tetano
Editor, Senior Moderator
J Med Virol
. 2023 Aug;95(8):e29040.
doi: 10.1002/jmv.29040. Co-delivery of a trimeric spike DNA and protein vaccine with aluminum hydroxide enhanced Th1-dominant humoral and cellular immunity against SARS-CoV-2
Hung-Chun Liao[SUP] 1 2 [/SUP], Min-Syuan Huang[SUP] 1 2 [/SUP], Fang-Feng Chiu[SUP] 1 [/SUP], Kit Man Chai[SUP] 1 [/SUP], Ching-Len Liao[SUP] 1 [/SUP], Suh-Chin Wu[SUP] 2 [/SUP], Hsin-Wei Chen[SUP] 1 3 4 [/SUP], Shih-Jen Liu[SUP] 1 3 4 [/SUP]
Affiliations
Protein subunit vaccines have been used as prophylactic vaccines for a long time. The well-established properties of these vaccines make them the first choice for the coronavirus disease 2019 (COVID-19) outbreak. However, it is not easy to develop a protein vaccine that induces cytotoxic T lymphocyte responses and requires a longer time for manufacturing, which limits the usage of this vaccine type. Here, we report the combination of a recombinant spike (S)-trimer protein with a DNA vaccine-encoded S protein as a novel COVID-19 vaccine. The recombinant S protein was formulated with different adjuvants and mixed with the DNA plasmid before injection. We found that the recombinant S protein formulated with the adjuvant aluminum hydroxide and mixed with the DNA plasmid could enhance antigen-specific antibody titers, neutralizing antibody titers. We further evaluated the IgG2a/IgG1 isotype and cytokine profiles of the specific boosted T-cell response, which indicated that the combined vaccine induced a T-helper 1 cell-biased immune response. Immunized hamsters were challenged with severe acute respiratory syndrome coronavirus 2, and the body weight of the hamsters that received the recombinant S protein with aluminum hydroxide and/or the DNA plasmid was not reduced. Alternatively, those that received control or only the DNA plasmid immunization were reduced. Interestingly, after the third day of the viral load in the lungs, the viral challenge could not be detected in hamsters immunized with the recombinant S protein in aluminum hydroxide mixed with DNA (tissue culture infectious dose < 10). The viral load in the lungs was 10[SUP]9[/SUP] , 10[SUP]6[/SUP] , and 10[SUP]7[/SUP] for the phosphate-buffered saline, protein in aluminum hydroxide, and DNA-only immunizations, respectively. These results indicated that antiviral mechanisms neutralizing antibodies play important roles. Furthermore, we found that the combination of protein and DNA vaccination could induce relatively strong CD8[SUP]+[/SUP] T-cell responses. In summary, the protein subunit vaccine combined with a DNA vaccine could induce strong CD8[SUP]+[/SUP] T-cell responses to increase antiviral immunity for disease control.
Keywords: COVID-19; DNA vaccine; SARS-CoV-2; subunit vaccine.
. 2023 Aug;95(8):e29040.
doi: 10.1002/jmv.29040. Co-delivery of a trimeric spike DNA and protein vaccine with aluminum hydroxide enhanced Th1-dominant humoral and cellular immunity against SARS-CoV-2
Hung-Chun Liao[SUP] 1 2 [/SUP], Min-Syuan Huang[SUP] 1 2 [/SUP], Fang-Feng Chiu[SUP] 1 [/SUP], Kit Man Chai[SUP] 1 [/SUP], Ching-Len Liao[SUP] 1 [/SUP], Suh-Chin Wu[SUP] 2 [/SUP], Hsin-Wei Chen[SUP] 1 3 4 [/SUP], Shih-Jen Liu[SUP] 1 3 4 [/SUP]
Affiliations
- PMID: 37635380
- DOI: 10.1002/jmv.29040
Protein subunit vaccines have been used as prophylactic vaccines for a long time. The well-established properties of these vaccines make them the first choice for the coronavirus disease 2019 (COVID-19) outbreak. However, it is not easy to develop a protein vaccine that induces cytotoxic T lymphocyte responses and requires a longer time for manufacturing, which limits the usage of this vaccine type. Here, we report the combination of a recombinant spike (S)-trimer protein with a DNA vaccine-encoded S protein as a novel COVID-19 vaccine. The recombinant S protein was formulated with different adjuvants and mixed with the DNA plasmid before injection. We found that the recombinant S protein formulated with the adjuvant aluminum hydroxide and mixed with the DNA plasmid could enhance antigen-specific antibody titers, neutralizing antibody titers. We further evaluated the IgG2a/IgG1 isotype and cytokine profiles of the specific boosted T-cell response, which indicated that the combined vaccine induced a T-helper 1 cell-biased immune response. Immunized hamsters were challenged with severe acute respiratory syndrome coronavirus 2, and the body weight of the hamsters that received the recombinant S protein with aluminum hydroxide and/or the DNA plasmid was not reduced. Alternatively, those that received control or only the DNA plasmid immunization were reduced. Interestingly, after the third day of the viral load in the lungs, the viral challenge could not be detected in hamsters immunized with the recombinant S protein in aluminum hydroxide mixed with DNA (tissue culture infectious dose < 10). The viral load in the lungs was 10[SUP]9[/SUP] , 10[SUP]6[/SUP] , and 10[SUP]7[/SUP] for the phosphate-buffered saline, protein in aluminum hydroxide, and DNA-only immunizations, respectively. These results indicated that antiviral mechanisms neutralizing antibodies play important roles. Furthermore, we found that the combination of protein and DNA vaccination could induce relatively strong CD8[SUP]+[/SUP] T-cell responses. In summary, the protein subunit vaccine combined with a DNA vaccine could induce strong CD8[SUP]+[/SUP] T-cell responses to increase antiviral immunity for disease control.
Keywords: COVID-19; DNA vaccine; SARS-CoV-2; subunit vaccine.