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<field name="value">Simões, Rachel Siqueira de Queiroz</field>
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<field name="value">Rodríguez Lázaro, David</field>
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<field name="confidence">600</field>
<field name="orcid_id">0000-0002-8795-854X</field>
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<field name="value">2023-03-31T09:45:29Z</field>
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<field name="value">2022-02</field>
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<field name="value">Several coronaviruses (CoVs) have been identified as human pathogens, including the&#xd;
α-CoVs strains HCoV-229E and HCoV-NL63 and the β-CoVs strains HCoV-HKU1 and HCoV-OC43.&#xd;
SARS-CoV, MERS-CoV, and SARS-CoV-2 are also classified as β-coronavirus. New SARS-CoV-2 spike&#xd;
genomic variants are responsible for human-to-human and interspecies transmissibility, consequences&#xd;
of adaptations of strains from animals to humans. The receptor-binding domain (RBD) of SARS-CoV-2&#xd;
binds to receptor ACE2 in humans and animal species with high affinity, suggesting there have been&#xd;
adaptive genomic variants. New genomic variants including the incorporation, replacement, or&#xd;
deletion of the amino acids at a variety of positions in the S protein have been documented and&#xd;
are associated with the emergence of new strains adapted to different hosts. Interactions between&#xd;
mutated residues and RBD have been demonstrated by structural modelling of variants including&#xd;
D614G, B.1.1.7, B1.351, P.1, P2; other genomic variants allow escape from antibodies generated by&#xd;
vaccines. Epidemiological and molecular tools are being used for real-time tracking of pathogen&#xd;
evolution and particularly new SARS-CoV-2 variants. COVID-19 vaccines obtained from classical and&#xd;
next-generation vaccine production platforms have entered clinicals trials. Biotechnology strategies&#xd;
of the first generation (attenuated and inactivated virus–CoronaVac, CoVaxin; BBIBP-CorV), second&#xd;
generation (replicating-incompetent vector vaccines–ChAdOx-1; Ad5-nCoV; Sputnik V; JNJ-78436735&#xd;
vaccine-replicating-competent vector, protein subunits, virus-like particles–NVX-CoV2373 vaccine),&#xd;
and third generation (nucleic-acid vaccines–INO-4800 (DNA); mRNA-1273 and BNT 162b (RNA&#xd;
vaccines) have been used. Additionally, dendritic cells (LV-SMENP-DC) and artificial antigenpresenting (aAPC) cells modified with lentiviral vector have also been developed to inhibit viral&#xd;
activity. Recombinant vaccines against COVID-19 are continuously being applied, and new clinical&#xd;
trials have been tested by interchangeability studies of viral vaccines developed by classical and&#xd;
next-generation platforms.</field>
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<field name="value">International Journal of Environmental Research and Public Health. 2022, V. 19, n. 4, 2392</field>
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<field name="value">https://doi.org/10.3390/ijerph19042392</field>
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<field name="value">Genomic variants</field>
<field name="value">Technological platforms</field>
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<field name="value">Classical and Next-Generation Vaccine Platforms to SARS-CoV-2: Biotechnological Strategies and Genomic Variants</field>
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<field name="value">International Journal of Environmental Research and Public Health</field>
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<field name="value">19</field>
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