Department of Biomedical Engineering, University at Buffalo, State University of New York, Buffalo, New York 14260, United States.
Department of Biochemistry and Biomedical Sciences, Michael G. DeGroote Institute for Infectious Diseases Research, McMaster Immunology Research Centre, McMaster University, Hamilton, Ontario L8S 4L8, Canada.
Mol Pharm. 2021 Feb 1;18(2):576-592. doi: 10.1021/acs.molpharmaceut.0c00383. Epub 2020 Aug 17.
Influenza viruses cause seasonal epidemics and represent a pandemic risk. With current vaccine methods struggling to protect populations against emerging strains, there is a demand for a next-generation flu vaccine capable of providing broad protection. Recombinant biotechnology, combined with nanomedicine techniques, could address this demand by increasing immunogenicity and directing immune responses toward conserved antigenic targets on the virus. Various nanoparticle candidates have been tested for use in vaccines, including virus-like particles, protein and carbohydrate nanoconstructs, antigen-carrying lipid particles, and synthetic and inorganic particles modified for antigen presentation. These methods have yielded some promising results, including protection in animal models against antigenically distinct influenza strains, production of antibodies with broad reactivity, and activation of potent T cell responses. Based on the evidence of current research, it is feasible that the next generation of influenza vaccines will combine recombinant antigens with nanoparticle carriers.
流感病毒会引发季节性流行,且存在引发大流行的风险。由于当前的疫苗接种方法难以保护人群免受新出现的毒株的侵害,因此需要开发能够提供广泛保护的新一代流感疫苗。重组生物技术与纳米医学技术相结合,通过提高免疫原性并将免疫反应引导到病毒上保守的抗原性靶标上,可能满足这一需求。已经有多种纳米颗粒候选物被测试用于疫苗,包括病毒样颗粒、蛋白质和碳水化合物纳米结构、携带抗原的脂质颗粒,以及为抗原呈递而修饰的合成和无机颗粒。这些方法已经取得了一些有前景的结果,包括在动物模型中针对具有不同抗原性的流感株的保护作用、产生具有广泛反应性的抗体以及激活有效的 T 细胞反应。根据目前研究的证据,下一代流感疫苗将重组抗原与纳米颗粒载体结合使用是可行的。