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A highly efficient needle-free-injection delivery system for mRNA-LNP vaccination against SARS-CoV-2.

Shanhong MaoShiyou LiYuxin ZhangLuoxin LongJunfeng PengYuanyan CaoJessica Z MaoXin QiQi XinGuoliang SanJing DingJun JiangXuejiao BaiQianting WangPengfei XuHuan XiaLijun LuLiangzhi XieDesheng KongShuangli ZhuWenbo Xu
Published in: Nano today (2022)
Despite the various vaccines that have been developed to combat the coronavirus disease 2019 (COVID-19) pandemic, the persistent and unpredictable mutations of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) require innovative and unremitting solutions to cope with the resultant immune evasion and establish a sustainable immune barrier. Here we introduce a vaccine-delivery system with a combination of a needle-free injection (NFI) device and a SARS-CoV-2-Spike-specific mRNA-Lipid Nanoparticle (LNP) vaccine. The benefits are duller pain and a significant increase of immunogenicity compared to the canonical needle injection (NI). From physicochemical and bioactivity analyses, the structure of the mRNA-LNP maintains stability upon NFI, contradictory to the belief that LNPs are inclined towards destruction under the high-pressure conditions of NFI. Moreover, mRNA-LNP vaccine delivered by NFI induces significantly more binding and neutralizing antibodies against SARS-CoV-2 variants than the same vaccine delivered by NI. Heterogeneous vaccination of BA.5-LNP vaccine with NFI enhanced the generation of neutralizing antibodies against Omicron BA.5 variants in rabbits previously vaccinated with non-BA.5-specific mRNA-LNP or other COVID-19 vaccines. NFI parameters can be adjusted to deliver mRNA-LNP subcutaneously or intramuscularly. Taken together, our results suggest that NFI-based mRNA-LNP vaccination is an effective substitute for the traditional NI-based mRNA-LNP vaccination.
Keyphrases
  • sars cov
  • respiratory syndrome coronavirus
  • coronavirus disease
  • binding protein
  • ultrasound guided
  • highly efficient
  • copy number
  • chronic pain
  • dengue virus
  • pain management
  • fatty acid
  • genome wide
  • dna binding