Intradermal administration of DNA vaccine targeting Omicron SARS-CoV-2 via pyro-drive jet injector provides the prolonged neutralizing antibody production via germinal center reaction.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
10 08 2023
Historique:
received: 08 03 2023
accepted: 06 08 2023
medline: 14 8 2023
pubmed: 11 8 2023
entrez: 10 8 2023
Statut: epublish

Résumé

Emerging SARS-CoV-2 Omicron variants are highly contagious with enhanced immune escape mechanisms against the initially approved COVID-19 vaccines. Therefore, we require stable alternative-platform vaccines that confer protection against newer variants of SARS-CoV-2. We designed an Omicron B.1.1.529 specific DNA vaccine using our DNA vaccine platform and evaluated the humoral and cellular immune responses. SD rats intradermally administered with Omicron-specific DNA vaccine via pyro-drive jet injector (PJI) thrice at 2-week intervals elicited high antibody titers against the Omicron subvariants as well as the ancestral strain. Indeed, the Omicron B.1.1.529-specific antibody titer and neutralizing antibody were higher than that of other strains. Longitudinal monitoring indicated that anti-spike (ancestral and Omicron) antibody titers decreased toward 30 weeks after the first vaccination dose. However, neutralization activity remained unaltered. Germinal center formation was histologically detected in lymph nodes in rats immunized with Omicron DNA vaccine. Ancestral spike-specific immune cell response was slightly weaker than Omicron spike-specific response in splenocytes with Omicron-adapted DNA vaccine, evaluated by ELISpot assay. Collectively, our findings suggest that Omicron targeting DNA vaccines via PJI can elicit robust durable antibody production mediated by germinal center reaction against this new variant as well as partially against the spike protein of other SARS-CoV-2 variants.

Identifiants

pubmed: 37563266
doi: 10.1038/s41598-023-40172-y
pii: 10.1038/s41598-023-40172-y
pmc: PMC10415318
doi:

Substances chimiques

Antibodies, Neutralizing 0
Vaccines, DNA 0
COVID-19 Vaccines 0
Antibodies, Viral 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

13033

Informations de copyright

© 2023. Springer Nature Limited.

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Auteurs

Hiroki Hayashi (H)

Department of Health Development and Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan. hayashih@cgt.med.osaka-u.ac.jp.

Jiao Sun (J)

Department of Health Development and Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Yuka Yanagida (Y)

Department of Health Development and Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Takako Otera (T)

Department of Health Development and Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Anges Inc., Tokyo, Japan.

Jiayu A Tai (JA)

Department of Device Application for Molecular Therapeutics, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Tomoyuki Nishikawa (T)

Department of Device Application for Molecular Therapeutics, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Kunihiko Yamashita (K)

Department of Device Application for Molecular Therapeutics, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Daicel Co, Osaka, Japan.

Naoki Sakaguchi (N)

Daicel Co, Osaka, Japan.

Shota Yoshida (S)

Department of Health Development and Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Department of Geriatric Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Satoshi Baba (S)

Department of Health Development and Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Department of Geriatric Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Chin Yang Chang (CY)

Department of Gene and Stem Cell Regenerative Therapy, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Munehisa Shimamura (M)

Department of Gene and Stem Cell Regenerative Therapy, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Department of Neurology, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Sachiko Okamoto (S)

Takara Bio Inc., Kusatsu, Shiga, Japan.

Yasunori Amaishi (Y)

Takara Bio Inc., Kusatsu, Shiga, Japan.

Hideto Chono (H)

Takara Bio Inc., Kusatsu, Shiga, Japan.

Junichi Mineno (J)

Takara Bio Inc., Kusatsu, Shiga, Japan.

Hiromi Rakugi (H)

Department of Geriatric Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Ryuichi Morishita (R)

Department of Clinical Gene Therapy, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.

Hironori Nakagami (H)

Department of Health Development and Medicine, Osaka University Graduate School of Medicine, Suita, Osaka, Japan.
Division of Microbiology and Immunology, Center for Infectious Disease Education and Research, Osaka University, Suita, Osaka, Japan.

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Classifications MeSH