mRNA vaccines against COVID‐19: a showcase for the importance of microbial biotechnology

• Published in: Microbial biotechnology Vol. 15; no. 1; pp. 135 - 148
• Main Author: Brüssow, Harald
• Format: Journal Article
• Language: English
• Published: United States John Wiley & Sons, Inc 01.01.2022; John Wiley and Sons Inc; Wiley
• Subjects: Aged; Antibodies; Biotechnology; Biotechnology industry; Chills; Collaboration; Coronaviruses; COVID-19; COVID-19 Vaccines; Drug dosages; Facial nerve; Fever; Glycoproteins; Headache; Heart diseases; Humans; Injection; Lipid composition; Lipids; Male; Medical research; Microorganisms; mRNA; mRNA Vaccines; Muscles; Muscular fatigue; Myocarditis; Nanoparticles; Neutralization; Nobel prizes; Observational studies; Pain; Pandemics; Paralysis; Physiology; Population studies; Populations; Protein composition; Protein expression; Proteins; RNA polymerase; SARS-CoV-2; Severe acute respiratory syndrome; Severe acute respiratory syndrome coronavirus 2; Special Issue; Spike Glycoprotein, Coronavirus; Spike protein; Uridine; Vaccine Efficacy; Vaccines; Vaccines, Synthetic; Viral diseases
• ISSN: 1751-7915; 1751-7915
• DOI: 10.1111/1751-7915.13974

Summary Pfizer‐BioNTech and Moderna developed in record time mRNA vaccines against COVID‐19 of high efficacy. The modest protection achieved with a similarly designed mRNA from CureVac underlines the importance of biotechnological details in formulation such as replacement of uridine by pseudouridine in the mRNA encoding the SARS‐CoV‐2 spike protein or the lipid composition of the nanoparticle coating the mRNA. Phase 3 vaccine trials and vaccine studies in special subject groups as well observational studies in whole populations confirmed the real‐world vaccine efficacy against symptomatic disease, particularly against severe COVID‐19 cases and to a lesser extent against mild SARS‐CoV‐2 infections. mRNA vaccine protection extended also to the alpha and beta variant viruses. The surge of delta variants led to an increase of infections and cases even in populations which achieved high vaccine coverage. This efficacy decline resulted to a lesser extent from a weaker neutralization of the delta variant but mostly from a waning vaccine protection over time. Data from Israel documented the efficacy of a third ‘booster’ injection 5 months after the second injection in older segments of the population. Adverse reactions consisted of transient injection site pain, headache, muscle pain, fatigue, fever and chills. Extensive surveillance studies documented a good safety profile revealing only a non‐significant increase in transient facial nerve paralysis and a significant, but modest increase in myocarditis in vaccinated young males that was lower than the myocarditis risk induced by SARS‐CoV‐2 infection.