Jangra Sonia, Lamoot Alexander, Singh Gagandeep, Laghlali Gabriel, Chen Yong, Yz Tingting, García-Sastre Adolfo, De Geest Bruno G, Schotsaert Michael
Department of Microbiology, Icahn School of Medicine at Mount Sinai New York, NY, USA.
Global Health and Emerging Pathogens Institute, Icahn School of Medicine at Mount Sinai New York, NY, USA.
bioRxiv. 2024 Jan 15:2024.01.14.575599. doi: 10.1101/2024.01.14.575599.
Adjuvants can enhance vaccine effectiveness of currently licensed influenza vaccines. We tested influenza vaccination in a mouse model with two adjuvants: Sendai virus derived defective interfering (SDI) RNA, a RIG-I agonist, and an amphiphilic imidazoquinoline (IMDQ-PEG-Chol), TLR7/8 adjuvant. The negatively charged SDI RNA was formulated into lipid nanoparticles (LNPs) facilitating the direct delivery of a RIG-I agonist to the cytosol. We have previously tested SDI and IMDQ-PEG-Chol as standalone and combination adjuvants for influenza and SARS-CoV-2 vaccines. Here we tested two different ionizable lipids, K-Ac7-Dsa and S-Ac7-Dog, for LNP formulations. The adjuvanticity of IMDQ-PEG-Chol with and without empty or SDI-loaded LNPs was validated in a licensed vaccine setting (quadrivalent influenza vaccine or QIV) against H1N1 influenza virus, showing robust induction of antibody titres and T cell responses. Depending on the adjuvant combination and LNP lipid composition (K-Ac7-Dsa or S-Ac7-Dog lipids), humoral and cellular vaccine responses could be tailored towards type 1 or type 2 host responses with specific cytokine profiles that correlated with protection during viral infection. The extent of protection conferred by different vaccine/LNP/adjuvant combinations was examined against challenge with the vaccine-matching strain of H1N1 influenza A virus. Groups that received either LNP formulated with SDI, IMDQ-PEG-Chol or both showed very low levels of viral replication in their lungs at five days post virus infection. LNP ionizable lipid composition as well as loading (empty versus SDI) also skewed host responses to infection, as reflected in the cytokine and chemokine levels in lungs of vaccinated animals upon infection. These studies show the potential of LNPs as adjuvant delivery vehicles for licensed vaccines and illustrate the importance of LNP composition for subsequent host responses to infection, an important point of consideration for vaccine safety.
佐剂可增强目前已获许可的流感疫苗的效力。我们在小鼠模型中用两种佐剂测试了流感疫苗接种:仙台病毒衍生的缺陷干扰(SDI)RNA,一种RIG-I激动剂,以及一种两亲性咪唑喹啉(IMDQ-PEG-Chol),TLR7/8佐剂。带负电荷的SDI RNA被制成脂质纳米颗粒(LNP),便于将RIG-I激动剂直接递送至胞质溶胶。我们之前已测试过SDI和IMDQ-PEG-Chol作为流感疫苗和SARS-CoV-2疫苗的单独及联合佐剂。在此,我们测试了用于LNP制剂的两种不同的可电离脂质,K-Ac7-Dsa和S-Ac7-Dog。在针对H1N1流感病毒的已获许可疫苗(四价流感疫苗或QIV)环境中,验证了含或不含空LNP或载有SDI的LNP的IMDQ-PEG-Chol的佐剂活性,显示出抗体滴度和T细胞反应的强劲诱导。根据佐剂组合和LNP脂质组成(K-Ac7-Dsa或S-Ac7-Dog脂质),体液和细胞疫苗反应可针对具有与病毒感染期间的保护相关的特定细胞因子谱的1型或2型宿主反应进行调整。针对疫苗匹配的甲型H1N1流感病毒株的攻击,检查了不同疫苗/LNP/佐剂组合所提供的保护程度。接受用SDI、IMDQ-PEG-Chol或两者配制的LNP的组在病毒感染后五天其肺部的病毒复制水平非常低。LNP可电离脂质组成以及负载情况(空LNP与载有SDI的LNP)也会使宿主对感染的反应发生偏差,这反映在感染后接种疫苗动物肺部的细胞因子和趋化因子水平上。这些研究显示了LNP作为已获许可疫苗的佐剂递送载体的潜力,并说明了LNP组成对于宿主随后对感染的反应的重要性,这是疫苗安全性的一个重要考虑点。