Department of Microbiology, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Department of Pharmaceutics, Ghent University, Ghent, Belgium.
Angew Chem Int Ed Engl. 2021 Apr 19;60(17):9467-9473. doi: 10.1002/anie.202015362. Epub 2021 Mar 11.
The search for vaccines that protect from severe morbidity and mortality because of infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the virus that causes coronavirus disease 2019 (COVID-19) is a race against the clock and the virus. Here we describe an amphiphilic imidazoquinoline (IMDQ-PEG-CHOL) TLR7/8 adjuvant, consisting of an imidazoquinoline conjugated to the chain end of a cholesterol-poly(ethylene glycol) macromolecular amphiphile. It is water-soluble and exhibits massive translocation to lymph nodes upon local administration through binding to albumin, affording localized innate immune activation and reduction in systemic inflammation. The adjuvanticity of IMDQ-PEG-CHOL was validated in a licensed vaccine setting (quadrivalent influenza vaccine) and an experimental trimeric recombinant SARS-CoV-2 spike protein vaccine, showing robust IgG2a and IgG1 antibody titers in mice that could neutralize viral infection in vitro and in vivo in a mouse model.
由于严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染导致的严重发病率和死亡率的疫苗寻找,是与时间和病毒的赛跑。在这里,我们描述了一种两亲性咪唑并喹啉(IMDQ-PEG-CHOL)TLR7/8 佐剂,由连接到胆固醇-聚(乙二醇)大分子两亲物链端的咪唑并喹啉组成。它是水溶性的,并且通过与白蛋白结合在局部给药时大量转移到淋巴结,从而提供局部先天免疫激活和减少全身炎症。IMDQ-PEG-CHOL 的佐剂活性在许可的疫苗环境(四价流感疫苗)和实验性三聚体重组 SARS-CoV-2 刺突蛋白疫苗中得到了验证,在小鼠中显示出强烈的 IgG2a 和 IgG1 抗体滴度,能够中和体外和体内的病毒感染在小鼠模型中。