tetano
Editor, Senior Moderator
Sci Rep
. 2024 Nov 9;14(1):27311.
doi: 10.1038/s41598-024-79122-7. Immunogenicity of intraperitoneal and intranasal liposome adjuvanted VLP vaccines against SARS-CoV-2 infection
Monrat Chulanetra[SUP] 1 [/SUP], Primana Punnakitikashem[SUP] 2 [/SUP], Kodchakorn Mahasongkram[SUP] 1 [/SUP], Wanpen Chaicumpa[SUP] 1 [/SUP], Kantaphon Glab-Ampai[SUP] 3 [/SUP]
Affiliations
Humans get SARS-CoV-2 infection mainly through inhalation; thus, vaccine that induces protective immunity at the virus entry site is important for early control of the infection. In this study, two anionic liposome (L)-adjuvanted VLP vaccines against SARS-CoV-2 were formulated. Baculovirus-Sf21 insect cell system was used for production of VLPs made of full-length S, M and E proteins. S protein of one vaccine (L-SME-VLPs) contained furin cleavage site at the S1/S2 junction, while that of another vaccine (L-S'ME-VLPs) did not. Both vaccines were innocuous and immunogenic when administered IP and IN to mice. Mice immunized IP with L-SME-VLPs/L-S'ME-VLPs (three doses, two-weeks intervals) had serum virus neutralizing (VN) antibodies (in falling order of isotype frequency): IgG3, IgA and IgG2a/IgG3, IgA and IgM, respectively. The L-S'ME VLPs vaccine induced significantly higher serum VN antibody titers than the L-SME-VLPs vaccine. All mice immunized IN with both vaccines had significant rise of VN antibodies in their bronchoalveolar lavage fluids (BALF). The VN antibodies in 67% of immunized mice were Th1- isotypes (IgG2a and/or IgG2b); the immunized mice had also other antibody isotypes in BALF. The intranasal L-S'ME-VLPs should be tested further step-by-step towards the clinical use as effective and safe vaccine against SARS-CoV-2.
Keywords: Antibody isotypes; Baculovirus-insect cell system; COVID-19; Liposome; SARS-CoV-2; VLP vaccines; Virus-like particles.
. 2024 Nov 9;14(1):27311.
doi: 10.1038/s41598-024-79122-7. Immunogenicity of intraperitoneal and intranasal liposome adjuvanted VLP vaccines against SARS-CoV-2 infection
Monrat Chulanetra[SUP] 1 [/SUP], Primana Punnakitikashem[SUP] 2 [/SUP], Kodchakorn Mahasongkram[SUP] 1 [/SUP], Wanpen Chaicumpa[SUP] 1 [/SUP], Kantaphon Glab-Ampai[SUP] 3 [/SUP]
Affiliations
- PMID: 39516286
- DOI: 10.1038/s41598-024-79122-7
Humans get SARS-CoV-2 infection mainly through inhalation; thus, vaccine that induces protective immunity at the virus entry site is important for early control of the infection. In this study, two anionic liposome (L)-adjuvanted VLP vaccines against SARS-CoV-2 were formulated. Baculovirus-Sf21 insect cell system was used for production of VLPs made of full-length S, M and E proteins. S protein of one vaccine (L-SME-VLPs) contained furin cleavage site at the S1/S2 junction, while that of another vaccine (L-S'ME-VLPs) did not. Both vaccines were innocuous and immunogenic when administered IP and IN to mice. Mice immunized IP with L-SME-VLPs/L-S'ME-VLPs (three doses, two-weeks intervals) had serum virus neutralizing (VN) antibodies (in falling order of isotype frequency): IgG3, IgA and IgG2a/IgG3, IgA and IgM, respectively. The L-S'ME VLPs vaccine induced significantly higher serum VN antibody titers than the L-SME-VLPs vaccine. All mice immunized IN with both vaccines had significant rise of VN antibodies in their bronchoalveolar lavage fluids (BALF). The VN antibodies in 67% of immunized mice were Th1- isotypes (IgG2a and/or IgG2b); the immunized mice had also other antibody isotypes in BALF. The intranasal L-S'ME-VLPs should be tested further step-by-step towards the clinical use as effective and safe vaccine against SARS-CoV-2.
Keywords: Antibody isotypes; Baculovirus-insect cell system; COVID-19; Liposome; SARS-CoV-2; VLP vaccines; Virus-like particles.