Shape-dependent adjuvanticity of nanoparticle-conjugated RNA adjuvants for intranasal inactivated influenza vaccines

Intranasal inactivated influenza vaccines can elicit mucosal immune responses that protect against virus infection. For the development of intranasal inactivated influenza vaccines, effective adjuvants inducing minimal adverse reactions are required. Generally, however, lower toxicity adjuvants have...

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Published in:RSC advances Vol. 8; no. 30; pp. 16527 - 16536
Main Authors: Tazaki, Taiyu, Tabata, Koshiro, Ainai, Akira, Ohara, Yuki, Kobayashi, Shintaro, Ninomiya, Takafumi, Orba, Yasuko, Mitomo, Hideyuki, Nakano, Tetsuo, Hasegawa, Hideki, Ijiro, Kuniharu, Sawa, Hirofumi, Suzuki, Tadaki, Niikura, Kenichi
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Language:English
Published: England Royal Society of Chemistry 01-01-2018
The Royal Society of Chemistry
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Abstract Intranasal inactivated influenza vaccines can elicit mucosal immune responses that protect against virus infection. For the development of intranasal inactivated influenza vaccines, effective adjuvants inducing minimal adverse reactions are required. Generally, however, lower toxicity adjuvants have lower adjuvanticity. In this research, we fabricated nanoparticle-based adjuvants to enhance its adjuvanticity. Herein, we focused on low-molecular-weight polyinosinic-polycytidylic acid, referred to as uPIC(40:400), as a weak and less toxic RNA adjuvant. We conjugated uPIC(40:400) with different shaped gold nanoparticles (AuNPs) electrostatically. Conjugation with gold nanorods, but not spherical AuNPs, markedly enhanced the adjuvanticity of uPIC(40:400), leading to the suppression of viral infection in mice. Notably, conjugation with gold nanorods did not increase the inflammatory cytokine production in dendritic cells. These data indicated that gold nanorods can provide a good platform for enhancing the weak adjuvanticity of uPIC(40:400) while maintaining low inflammatory cytokine production toward the development of intranasal inactivated influenza vaccines.
AbstractList Intranasal inactivated influenza vaccines can elicit mucosal immune responses that protect against virus infection. For the development of intranasal inactivated influenza vaccines, effective adjuvants inducing minimal adverse reactions are required. Generally, however, lower toxicity adjuvants have lower adjuvanticity. In this research, we fabricated nanoparticle-based adjuvants to enhance its adjuvanticity. Herein, we focused on low-molecular-weight polyinosinic-polycytidylic acid, referred to as uPIC(40:400), as a weak and less toxic RNA adjuvant. We conjugated uPIC(40:400) with different shaped gold nanoparticles (AuNPs) electrostatically. Conjugation with gold nanorods, but not spherical AuNPs, markedly enhanced the adjuvanticity of uPIC(40:400), leading to the suppression of viral infection in mice. Notably, conjugation with gold nanorods did not increase the inflammatory cytokine production in dendritic cells. These data indicated that gold nanorods can provide a good platform for enhancing the weak adjuvanticity of uPIC(40:400) while maintaining low inflammatory cytokine production toward the development of intranasal inactivated influenza vaccines.
Intranasal inactivated influenza vaccines can elicit mucosal immune responses that protect against virus infection. For the development of intranasal inactivated influenza vaccines, effective adjuvants inducing minimal adverse reactions are required. Generally, however, lower toxicity adjuvants have lower adjuvanticity. In this research, we fabricated nanoparticle-based adjuvants to enhance its adjuvanticity. Herein, we focused on low-molecular-weight polyinosinic-polycytidylic acid, referred to as uPIC(40:400), as a weak and less toxic RNA adjuvant. We conjugated uPIC(40:400) with different shaped gold nanoparticles (AuNPs) electrostatically. Conjugation with gold nanorods, but not spherical AuNPs, markedly enhanced the adjuvanticity of uPIC(40:400), leading to the suppression of viral infection in mice. Notably, conjugation with gold nanorods did not increase the inflammatory cytokine production in dendritic cells. These data indicated that gold nanorods can provide a good platform for enhancing the weak adjuvanticity of uPIC(40:400) while maintaining low inflammatory cytokine production toward the development of intranasal inactivated influenza vaccines. Conjugation with gold nanorods enhanced the adjuvanticity of RNA adjuvant for intranasal inactivated influenza vaccines, providing efficient protection against infection in mice.
Author Tabata, Koshiro
Suzuki, Tadaki
Ninomiya, Takafumi
Niikura, Kenichi
Ijiro, Kuniharu
Kobayashi, Shintaro
Orba, Yasuko
Ohara, Yuki
Nakano, Tetsuo
Sawa, Hirofumi
Tazaki, Taiyu
Hasegawa, Hideki
Mitomo, Hideyuki
Ainai, Akira
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  organization: Department of Pathology, National Institute of Infectious Diseases Toyama 1-23-1, Shinjuku-ku Tokyo 162-8640 Japan tksuzuki@nih.go.jp
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  fullname: Orba, Yasuko
  organization: Research Center for Zoonosis Control, Hokkaido University Sapporo 001-0020 Japan
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  givenname: Hideyuki
  orcidid: 0000-0002-6748-7816
  surname: Mitomo
  fullname: Mitomo, Hideyuki
  organization: Global Station for Soft Matter, Global Institution for Collaborative Research and Education (GI-CoRE), Hokkaido University Sapporo 001-0021 Japan
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  givenname: Tetsuo
  orcidid: 0000-0001-8324-2109
  surname: Nakano
  fullname: Nakano, Tetsuo
  organization: Graduate School of Agriculture, Hokkaido University Sapporo 060-8589 Japan
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  givenname: Hideki
  surname: Hasegawa
  fullname: Hasegawa, Hideki
  email: tksuzuki@nih.go.jp
  organization: Department of Pathology, National Institute of Infectious Diseases Toyama 1-23-1, Shinjuku-ku Tokyo 162-8640 Japan tksuzuki@nih.go.jp
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  fullname: Ijiro, Kuniharu
  organization: Global Station for Soft Matter, Global Institution for Collaborative Research and Education (GI-CoRE), Hokkaido University Sapporo 001-0021 Japan
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  orcidid: 0000-0003-2569-2755
  surname: Sawa
  fullname: Sawa, Hirofumi
  organization: Global Station for Zoonosis Control, Global Institution for Collaborative Research and Education (GI-CoRE), Hokkaido University Sapporo 001-0020 Japan
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  givenname: Tadaki
  surname: Suzuki
  fullname: Suzuki, Tadaki
  email: tksuzuki@nih.go.jp
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  orcidid: 0000-0002-2874-4920
  surname: Niikura
  fullname: Niikura, Kenichi
  email: niikura.kenichi@nit.ac.jp
  organization: Department of Innovative Systems Engineering, Nippon Institute of Technology 4-1 Gakuendai, Miyashiro-machi, Minamisaitama-gun Saitama 345-8501 Japan niikura.kenichi@nit.ac.jp
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Snippet Intranasal inactivated influenza vaccines can elicit mucosal immune responses that protect against virus infection. For the development of intranasal...
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StartPage 16527
SubjectTerms Adjuvants
Chemistry
Conjugation
Cytokines
Gold
Influenza
Molecular chains
Nanoparticles
Nanorods
Ribonucleic acid
RNA
Toxicity
Vaccines
Viruses
Title Shape-dependent adjuvanticity of nanoparticle-conjugated RNA adjuvants for intranasal inactivated influenza vaccines
URI https://www.ncbi.nlm.nih.gov/pubmed/35540526
https://www.proquest.com/docview/2036818670
https://search.proquest.com/docview/2662547298
https://pubmed.ncbi.nlm.nih.gov/PMC9080258
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