4.8 Article

Enhanced Immune Responses by Virus-Mimetic Polymeric Nanostructures Against Infectious Diseases

Journal

FRONTIERS IN IMMUNOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.804416

Keywords

subunit vaccines; virus-mimetic polymeric nanostructures; multivalent epitope; molecular adjuvants; enhanced immune responses

Categories

Funding

  1. National Natural Science Foundation of China [22101086, 21961142018, U1832220, 51873067]
  2. Natural Science Foundation of Guangdong Province [2021A1515010271, 2021A1515012024]

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Virus-mimetic polymeric nanostructures are a promising platform for enhanced immune responses and disease prevention. Using polymers as templates, various biomimetic structures can be designed and loaded with suitable antigens and metal oxide clusters to mimic the size and surface antigenicity of viruses. These structures can promote potent immune responses to protect humans from pathogens.
Intermittent outbreaks of global pandemic disease have spurred new sensors and medicines development for the prevention of disease spread. This perspective specifically covers recent advances, challenges, and future directions in virus-mimetic polymeric nanostructures and their application in biological medicines with a special emphasis on subunit vaccine development. With tailorable compositions and properties, polymers facilitate the ingenious design of various polymeric nanostructures. As one type of polymeric nanostructures, virus-mimetic polymeric nanostructures have been developed as an attractive platform for enhanced immune responses, since they combine the merits of polymer nanocores with the biomimetic characteristic of virus which displays multivalent epitopes on their surfaces. This perspective also provides an applicative approach to rationally design virus-mimetic polymeric platforms based on nanostructures that are self-assembled by using polymers as templates and the antigens and metal oxide clusters loaded on their surface to mimic viruses in size and surface antigenicity. Sub-200 nm virus-mimetic polymeric nanostructures are in a relatively lower level of endotoxins and can promote the antigens to elicit potent humoral and cellular immune responses against pathogenic bacteria. The promising development of virus-mimetic polymeric nanostructures will continue to protect human health from common pathogens and emerging infectious threats.

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