Vaccines’ Safety and Effectiveness in the Midst of Covid-19 Mutations

Abstract

We examined the coronavirus classification and evolution through its multiple mutations that have increased its transmissibility rate up to 70% globally, threatening to undermine the promise of a number of emerging vaccines that primarily focus on the immune detection of the Spike trimer. The safety and effectiveness of different vaccination methods are evaluated and compared, including the mRNA version, the Adenovirus DNA, Spike protein subunits, the deactivated virus genres, and the live attenuated coronavirus. Mutations have been long considered as random events, or mistakes during the viral RNA replication. Usually, what can go wrong will go wrong; therefore, repeated transformations lead to the extinction of a virus. On the contrary, the aggregate result of over 300,000 Covid-19 variants has expanded its transmis-sibility and infectiousness. Covid-19 mutations do not degrade the virus; they empower and facilitate its disguise to evade detection. Unlike other coro-naviruses, Covid-19 amino acid switches do not reflect the random unfolding of errors that eventually eradicate the virus. Covid-19 appears to use mutations adaptively in the service of its survival and expansion. We cite evidence that Covid-19 inhibits the interferon type I production, compromising adap-tive immunity from recognizing the virus. The deleterious consequences of the cytokine storm where the CD8 + killer cells injure the vital organs of the host may well be a Covid-19 manoeuvring to escape exposure. It is probable that evolution has programmed Covid-19 with an adeptness designed to de-bilitate key systemic defences to secure its subsistence. To date the infec-tiousness of the Covid-19 pandemic is exponentially increasing, denoting the possibility of an even more dangerously elusive, inconspicuous, and sophisticated version of the disease. How to cite this paper: Sofra, X. (2021) Vaccines' Safety and Effectiveness in the Midst of Covid-19 Mutations. Health, 13, 283-298. https://doi.