Abstract

Infection with Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) causes Coronavirus Disease 2019 (COVID-19), which has reached pandemic proportions. A number of effective vaccines have been produced, including mRNA vaccines and viral vector vaccines, which are now being implemented on a large scale in order to control the pandemic. The mRNA vaccines are composed of viral Spike S1 protein encoding mRNA incorporated in a lipid nanoparticle and stabilized by polyethylene glycol (PEG). The mRNA vaccines are novel in many respects, including cellular uptake and the intracellular routing, processing, and secretion of the viral protein. Viral vector vaccines have incorporated DNA sequences, encoding the SARS-CoV-2 Spike protein into (attenuated) adenoviruses. The antigen presentation routes in MHC class I and class II, in relation to the induction of virus-neutralizing antibodies and cytotoxic T-lymphocytes, will be reviewed. In rare cases, mRNA vaccines induce unwanted immune mediated side effects. The mRNA-based vaccines may lead to an anaphylactic reaction. This reaction may be triggered by PEG. The intracellular routing of PEG and potential presentation in the context of CD1 will be discussed. Adenovirus vector-based vaccines have been associated with thrombocytopenic thrombosis events. The anti-platelet factor 4 antibodies found in these patients could be generated due to conformational changes of relevant epitopes presented to the immune system.

Highlights

  • Covishield) and Jansen/Johnson and Johnson (Ad26.COV2.S, brand name Janssen COVID19 Vaccine), as well as the Sputnik-V and CanSino vaccines. Both mRNA vaccines for SARS-CoV-2 as well as viral vector based vaccines have turned out to be highly effective for protection against mild and severe COVID-19 cases

  • The following is a description of the methodology to optimize some mRNA elements, which is based on references cited in publications reporting initial results for SARS-CoV-2 vaccine trials

  • High protein expression levels were observed in mice, pigs, and non-human primates injected with mRNAs containing unmodified nucleosides

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Summary

Introduction with regard to jurisdictional claims in

Has triggered the rapid development of vaccines against its causative agent, Severe Acute. Covishield) and Jansen/Johnson and Johnson (Ad26.COV2.S, brand name Janssen COVID19 Vaccine), as well as the Sputnik-V and CanSino vaccines. Both mRNA vaccines for SARS-CoV-2 as well as viral vector based vaccines have turned out to be highly effective for protection against mild and severe COVID-19 cases. While SARS-CoV-2 vaccines are protecting from the severe illness and deaths due to COVID-19, after large-scale implementation, rare immune-mediated side effects became apparent. Anaphylactic reactions and various thrombotic or abnormal bleeding have raised concern [8,9] These side effects may be due to abnormal handling or presentation of the vaccine or vaccine additives to the immune system, of which the potential scenarios will be discussed

Presentation of SARS-CoV-2 Antigens during COVID-19
Schematic
Protein Sequence
Immune Response
Adenoviral Vector
Unconventional Antigen Presentation Molecules
Hypersensitivity and PEG Antigen Presentation
Antigen Presentation of PEG
Possible Mechanisms or Etiology of Vaccine-Induced ITP
Conclusions
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