4.5 Editorial Material

Post-genomic platform for development of oligonucleotide vaccines against RNA viruses: diamond cuts diamond

期刊

INFLAMMATION RESEARCH
卷 71, 期 7-8, 页码 729-739

出版社

SPRINGER BASEL AG
DOI: 10.1007/s00011-022-01582-2

关键词

Oligonucleotide vaccine; SARS-CoV-2; RNA viruses; Immunity; Pandemic; Post-genomic platform; La-S-so

资金

  1. V.I. Vernadsky Crimean Federal University [FZEG-2021-0009, 121102900145-0]

向作者/读者索取更多资源

The coronavirus pandemic highlights the need for effective vaccines against viral diseases. New platforms for vaccine creation, such as adenovirus vectors and mRNA vaccines, have shown potential in preventing coronavirus infection. However, these platforms have the disadvantage of limited antigen presentation, allowing the virus to evade immunity. The development of new vaccine platforms that can adapt to virus subtypes is urgently needed.
The coronavirus pandemic has starkly demonstrated the need to create highly effective vaccines against various viral diseases. The emerging new platforms for vaccine creation (adenovirus vectors and mRNA vaccines) have shown their worth in the fight against the prevention of coronavirus infection. However, adenovirus vectors and mRNA vaccines have a serious disadvantage: as a rule, only the S protein of the coronavirus is presented as an antigen. This tactic for preventing infection allows the ever-mutating virus to escape quickly from the immunity protection provided by such vaccines. Today, viral genomic databases are well-developed, which makes it possible to create new vaccines on a fundamentally new post-genomic platform. In addition, the technology for the synthesis of nucleic acids is currently experiencing an upsurge in demand in various fields of molecular biology. The accumulated experience suggests that the unique genomic sequences of viruses can act as antigens that trigger powerful humoral and cellular immunity. To achieve this effect, the following conditions must be created: the structure of the nucleic acid must be single-stranded, have a permanent 3D nanostructure, and have a unique sequence absent in the vaccinated organism. Oligonucleotide vaccines are able to resist the rapidly changing genomic sequences of RNA viruses by using conserved regions of their genomes to generate a long-term immune response, acting according to the adage that a diamond cuts a diamond. In addition, oligonucleotide vaccines will not contribute to antibody-dependent enhanced infection, since the nucleic acid of the coronavirus is inside the viral particle. It is obvious that new epidemics and pandemics caused by RNA viruses will continue to arise periodically in the human population. The creation of new, safe, and effective platforms for the production of vaccines that can flexibly change and adapt to new subtypes of viruses is very urgent and at this moment should be considered as a strategically necessary task.

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