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Biomedical innovations to combat COVID-19 edited by Sergio Rosales-Mendoza, Mauricio Comas-Garcia and Omar Gonzalez-Ortega
- Format:
- Book
- Language:
- English
- Subjects (All):
- COVID-19 (Disease)--Treatment.
- COVID-19 (Disease).
- COVID-19 (Disease)--Diagnosis.
- Physical Description:
- 1 online resource
- Place of Publication:
- London Academic Press [2022]
- Contents:
- Front Cover
- Biomedical Innovations to Combat COVID-19
- Copyright Page
- Contents
- List of contributors
- Preface
- Acknowledgments
- 1 Basic virological aspects of SARS-CoV-2
- 1.1 Introduction
- 1.2 Genome organization and function
- 1.2.1 Genome organization
- 1.2.2 Genome function
- 1.3 Viral entry
- 1.3.1 Virus-cell interaction
- 1.3.2 Clathrin-mediated endocytosis
- 1.4 Genome replication and translation
- 1.4.1 Replication and transcription
- 1.4.2 Translation
- 1.5 Assembly
- 1.5.1 Virus-induced cell remodeling
- 1.5.2 Virion assembly
- 1.6 Egress
- 1.6.1 A novel egress pathway
- 1.7 General aspects of the immune response to a viral infection
- 1.7.1 Type I interferon and the antiviral state
- 1.7.2 Dendritic cells
- 1.7.3 Natural killer cells
- 1.7.4 Macrophages
- 1.7.5 Cellular immune response
- 1.7.6 The humoral immune response
- 1.8 Concluding remarks
- References
- 2 Fundamental aspects of the structural biology of coronaviruses
- 2.1 Introduction
- 2.2 The structural proteins
- 2.2.1 Envelope protein
- 2.2.2 Nucleocapsid protein
- 2.2.3 Membrane protein
- 2.2.4 Spike protein
- 2.3 The viral proteases
- 2.3.1 Main protease
- 2.3.2 Papain-like protease
- 2.4 The accessory proteins
- 2.4.1 Protein 3a
- 2.4.2 Protein 7a
- 2.4.3 Protein 8
- 2.4.4 Protein 9b
- 2.5 Concluding remarks
- 3 Introduction to the SARS-CoV-2/COVID-19 epidemiology
- 3.1 Introduction
- 3.2 Epidemiology
- 3.3 Clinical characteristics
- 3.3.1 Definition of a suspected case established by the WHO
- 3.4 Impact of COVID-19
- 3.5 Infection in pediatrics
- 3.6 Vitamin D and COVID-19
- 3.7 Epidemiology analysis of the SARS-CoV-2 outbreak
- 3.8 Immune response and reinfections
- 3.9 SARS-CoV-2 variants
- 3.10 Closing remarks
- References
- 4 Structural biology of the SARS-CoV-2 replisome: evolutionary and therapeutic implications
- 4.1 Introduction
- 4.2 Structural biology of SARS-CoV-2
- 4.3 The SARS-CoV-2 replisome: expanding knowledge through structural biology
- 4.4 The RNA-dependent RNA polymerase
- 4.5 Nsp7 and nsp8 processivity actors
- 4.6 Nsp13 helicase
- 4.7 Nsp14 exonuclease and N7-methyltransferase
- 4.8 Nsp9 single-stranded RNA-binding protein
- 4.9 Nsp10-nsp14 and nsp16 cofactor
- 4.10 The nonenzymatic synthesis of nucleosides and their derivatives: from the prebiotic chemistry to therapeutic agents
- 4.11 On the origin and early evolution of RNA viruses and SARS-CoV-2
- 4.12 The emergence of new infectious diseases by zoonoses
- 4.13 Conclusion
- 5 Clinical progression of patients with COVID-19: the impact of the pandemic in Latin America
- 5.1 Introduction
- 5.2 COVID-19-associated pathogenesis
- 5.2.1 The SARS-CoV-2 effect on multiple organs is associated with ACE2 expression
- 5.2.2 Underlying comorbidities and lethality
- 5.2.3 The clinical usefulness of clustering symptoms
- 5.3 COVID-19 behavior in Latin America
- 5.3.1 Viral outbreaks in Latin America
- 5.3.2 Latin America: the epicenter of COVID-19
- 5.3.3 Underlying comorbidities in Latin America
- 5.3.4 Most common COVID-19 symptoms in Latin America
- 5.4 COVID-19 in Mexico
- 5.4.1 COVID-19 in Mexico: lethality, comorbidities and symptoms
- 5.5 Remarks
- 6 Overview of the immune response against SARS-CoV-2
- 6.1 Introduction
- 6.2 Virion structure
- 6.3 Viral cycle
- 6.3.1 Transcription and translation
- 6.3.2 Replication complex of SARS-CoV-2
- 6.3.3 Egress
- 6.4 Protein organization of SARS-CoV-2
- 6.4.1 Spike protein
- 6.4.2 Nucleocapsid protein
- 6.5 The innate immune response against SARS-CoV-2
- 6.5.1 Evasion mechanisms
- 6.6 The immune response against SARS-CoV-2
- 6.6.1 Humoral immunity against SARS-CoV-2 infection
- 6.7 Neutralizing antibodies
- 6.8 Immunopathology of COVID-19
- 6.9 Conclusion
- Acknowledgment
- Conflicts of interest
- 7 Viral-vectored vaccines against SARS-CoV-2
- 7.1 Introduction
- 7.2 Development of COVID-19 vaccines
- 7.2.1 COVID-19 vaccines breaking record times to first-in-human trials
- 7.2.2 Classical versus next-generation vaccine platforms
- 7.2.2.1 Classical vaccine platforms
- 7.2.2.2 Next-generation vaccine platforms
- 7.2.3 COVID-19 vaccine pipelines in clinical evaluation and viral-vectored vaccines
- 7.2.4 Leading viral-vectored vaccine candidates in Phase III trial
- 7.3 Concluding remarks
- 8 RNA-based vaccines against SARS-CoV-2
- 8.1 Introduction
- 8.2 Principles of mRNA vaccines
- 8.3 Liposomes as vaccine delivery vehicles
- 8.3.1 Synthesis of liposomes
- 8.3.2 Modification of liposomes
- 8.4 The mRNA-1273 vaccine developed by Moderna Inc
- 8.4.1 SARS-CoV-2-S-2P mRNA synthesis and lipid nanoparticle formulation
- 8.4.2 Preclinical trial: mouse studies
- 8.4.3 Phase I
- 8.4.4 Preclinical trial: nonhuman primates
- 8.4.5 Phase I: older adults
- 8.4.6 Phase III
- 8.5 BNT162b1 and BNT162b2 vaccines developed by Pfizer and BioNTech
- 8.5.1 Preclinical trial
- 8.5.2 Phase I/II
- 8.5.2.1 German trial (NCT04380701, EudraCT:2020-001038-36)
- 8.5.3 Phase I trial including older adults and BNT162b2
- 8.5.3.1 ClinicalTrials.gov identifier, NCT04368728
- 8.5.4 Decision between the two vaccine candidates BNT162
- 8.5.5 Phase II/III: BNT162b2
- 8.6 CVnCoV vaccine developed by CureVac
- 8.6.1 Preclinical trials
- 8.6.2 Mice
- 8.6.3 Syrian hamster
- 8.6.4 Rhesus macaques
- 8.6.5 Phase I
- 8.7 Concluding remarks and perspectives
- 9 Particulate vaccines against SARS-CoV-2
- 9.1 Introduction
- 9.1.1 The COVID-19 pandemic
- 9.1.2 A severe contagious disease
- 9.1.3 Characteristics of SARS-CoV-2
- 9.2 Vaccines in development
- 9.2.1 Vaccines against SARS-CoV-2
- 9.2.2 Vaccines in clinical trials
- 9.2.3 On the vaccines under development
- 9.3 Particulate vaccines
- 9.3.1 Definitions and existing reports
- 9.3.2 Benefits of nanovaccines and considerations
- 9.4 Vaccines based on lipid nanoparticles
- 9.5 Inorganic nanoparticles as carriers
- 9.5.1 Composition and synthesis
- 9.5.2 Gold, silver, and iron oxide nanoparticles
- 9.6 Nanovaccines against SARS-CoV-2
- 9.7 Concluding remarks
- 10 Virus-like particle-based vaccines against SARS-CoV-2
- 10.1 Introduction
- 10.2 Potential of VLP-based vaccines
- 10.3 HBV vaccines
- 10.4 HEV vaccines
- 10.5 HPV vaccines
- 10.6 Precedents of VLP-based vaccines against human coronaviruses
- 10.7 VLP-based vaccines against SARS-CoV-2
- 10.8 Concluding remarks
- Funding
- 11 Innovative recombinant protein-based vaccines against SARS-CoV-2
- 11.1 Introduction
- 11.2 SARS-CoV, the vaccines proposed before COVID-19
- 11.3 Current vaccines proposed for SARS-CoV-2
- 11.4 Vaccine platforms implemented for SARS-CoV-2
- 11.5 SARS-CoV-2 protein-based vaccines
- 11.6 The rational design of the antigen by bioinformatics strategies
- 11.7 Current vaccine candidates based on recombinant proteins
- 11.8 The NVX-CoV2373 vaccine
- 11.9 Preclinical trials
- 11.9.1 Mouse studies
- 11.10 Nonhuman primates studies
- 11.10.1 Olive baboons
- 11.10.2 Cynomolgus macaques
- 11.11 Clinical trials
- 11.12 The VAT00002 vaccine
- 11.12.1 Clinical trial
- 11.13 The ZF2001 vaccine
- 11.13.1 Clinical trial
- 11.14 Efforts to develop a vaccine in Mexico
- 11.15 Concluding remarks and perspectives
- Notes:
- Print version record
- Other Format:
- Print version:
- Print version Biomedical innovations to combat COVID-19
- Print version BIOMEDICAL INNOVATIONS TO COMBAT COVID-19
- ISBN:
- 9780323902496
- 0323902499
- OCLC:
- 1277276275
- Access Restriction:
- Restricted for use by site license
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