Coleman Christopher M, Venkataraman Thiagarajan, Liu Ye V, Glenn Gregory M, Smith Gale E, Flyer David C, Frieman Matthew B
University of Maryland, School of Medicine, 685 West Baltimore St, Baltimore, MD 21201, United States.
Novavax, Inc., 22 Firstfield Rd, Gaithersburg, MD 20852, United States.
Vaccine. 2017 Mar 14;35(12):1586-1589. doi: 10.1016/j.vaccine.2017.02.012. Epub 2017 Feb 23.
The Middle East respiratory syndrome coronavirus (MERS-CoV) was first discovered in late 2012 and has gone on to cause over 1800 infections and 650 deaths. There are currently no approved therapeutics or vaccinations for MERS-CoV. The MERS-CoV spike (S) protein is responsible for receptor binding and virion entry to cells, is immunodominant and induces neutralizing antibodies in vivo, all of which, make the S protein an ideal target for anti-MERS-CoV vaccines. In this study, we demonstrate protection induced by vaccination with a recombinant MERS-CoV S nanoparticle vaccine and Matrix-M1 adjuvant combination in mice. The MERS-CoV S nanoparticle vaccine produced high titer anti-S neutralizing antibody and protected mice from MERS-CoV infection in vivo.
中东呼吸综合征冠状病毒(MERS-CoV)于2012年末首次被发现,已导致超过1800例感染和650例死亡。目前尚无针对MERS-CoV的获批治疗方法或疫苗。MERS-CoV刺突(S)蛋白负责受体结合和病毒粒子进入细胞,具有免疫显性并在体内诱导中和抗体,所有这些特性使S蛋白成为抗MERS-CoV疫苗的理想靶点。在本研究中,我们证明了重组MERS-CoV S纳米颗粒疫苗与Matrix-M1佐剂联合接种在小鼠中诱导的保护作用。MERS-CoV S纳米颗粒疫苗产生了高滴度的抗S中和抗体,并在体内保护小鼠免受MERS-CoV感染。