Moderna Inc., Cambridge, MA, USA.
Department of Pathology, University of Texas Medical Branch, Galveston, TX, USA.
Sci Adv. 2023 Sep 22;9(38):eadh1655. doi: 10.1126/sciadv.adh1655.
Intranasal vaccination represents a promising approach for preventing disease caused by respiratory pathogens by eliciting a mucosal immune response in the respiratory tract that may act as an early barrier to infection and transmission. This study investigated immunogenicity and protective efficacy of intranasally administered messenger RNA (mRNA)-lipid nanoparticle (LNP) encapsulated vaccines against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in Syrian golden hamsters. Intranasal mRNA-LNP vaccination systemically induced spike-specific binding [immunoglobulin G (IgG) and IgA] and neutralizing antibodies. Intranasally vaccinated hamsters also had decreased viral loads in the respiratory tract, reduced lung pathology, and prevented weight loss after SARS-CoV-2 challenge. Together, this study demonstrates successful immunogenicity and protection against respiratory viral infection by an intranasally administered mRNA-LNP vaccine.
鼻腔接种代表了一种很有前途的方法,通过在呼吸道中引发黏膜免疫反应来预防呼吸道病原体引起的疾病,这种反应可以作为感染和传播的早期屏障。本研究调查了鼻腔内给予信使 RNA(mRNA)-脂质纳米颗粒(LNP)包裹疫苗对叙利亚金黄地鼠严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)的免疫原性和保护效果。鼻腔内 mRNA-LNP 疫苗接种系统地诱导了刺突特异性结合[免疫球蛋白 G(IgG)和 IgA]和中和抗体。鼻腔内接种疫苗的仓鼠在 SARS-CoV-2 攻击后呼吸道中的病毒载量也降低,肺部病理减少,体重减轻也得到了预防。总之,这项研究证明了鼻腔内给予的 mRNA-LNP 疫苗具有成功的免疫原性和针对呼吸道病毒感染的保护作用。
Proc Natl Acad Sci U S A. 2022-6-14
Cell Host Microbe. 2021-2-10
Vaccines (Basel). 2025-7-23
Mol Ther Nucleic Acids. 2025-8-8
mBio. 2025-8-13
Front Immunol. 2025-6-6
Mol Ther Nucleic Acids. 2025-4-24
Nature. 2025-5
Npj Viruses. 2024-8-22
Sci Immunol. 2022-10-28
Mucosal Immunol. 2022-4
EBioMedicine. 2022-2