Efficacy, Safety, and Immunogenicity of Vaccines against Viruses: From Network Medicine to Clinical Experimentation 2nd Edition

A special issue of Viruses (ISSN 1999-4915). This special issue belongs to the section "Viral Immunology, Vaccines, and Antivirals".

Deadline for manuscript submissions: closed (20 April 2024) | Viewed by 2181

Special Issue Editors


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Guest Editor
Biomedical Research Center, National Institute on Aging, National Institutes of Health, Bethesda, MD 21224, USA
Interests: computational bioinformatics; applied data science; machine learning
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Guest Editor
Department of Experimental and Clinical Medicine, University of Catanzaro, 88100 Catanzaro, Italy
Interests: bioinformatics; network analysis; biological data analysis; COVID-19
Special Issues, Collections and Topics in MDPI journals

Special Issue Information

Dear Colleagues,

Despite the availability of effective vaccines against many diseases (e.g., COVID-19, Influenza, Varicella Virus, HPV), there is a need to study both novel and the existing vaccines and create prioritization campaigns to maintain vaccine-induced protection against variant strains and breakthrough infections.

Bioinformatics and network medicine help the research community to investigate the efficacy, safety and immunogenicity of vaccines and the mutual relationships among them.

An increasing body of evidence confirms that the synergistic integration of network medicine and clinical experimentation may improve the quality of existing vaccines as well as the development of novel ones. This Special Issue aims to foster discussion on following topics:

  • Development of novel vaccines;
  • Study of the immunogenicity of existing vaccines;
  • Age- and sex-based differences;
  • Introduction of novel prioritisation methods.

Dr. Pietro Hiram Guzzi
Dr. Jayanta Kumar Das
Dr. Marianna Milano
Guest Editors

Manuscript Submission Information

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Keywords

  • vaccines
  • vaccine security
  • computational bioinformatics
  • network analysis
  • data science

Published Papers (2 papers)

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Review

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11 pages, 250 KiB  
Review
Evaluation of Vaccine Immunogenicity—Correlates to Real-World Protection: Influenza
by Csaba Laszlofy, Gyorgy Fazekas, Zoltan Barath and Zoltan Vajo
Viruses 2024, 16(3), 441; https://doi.org/10.3390/v16030441 - 12 Mar 2024
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Abstract
Recent events highlighted that, despite decades of studying vaccine immunogenicity and efforts toward finding correlates of protection, evaluating real-world vaccine efficacy as well as establishing meaningful licensing criteria still represents a significant challenge. In this paper, we review all aspects of influenza vaccine [...] Read more.
Recent events highlighted that, despite decades of studying vaccine immunogenicity and efforts toward finding correlates of protection, evaluating real-world vaccine efficacy as well as establishing meaningful licensing criteria still represents a significant challenge. In this paper, we review all aspects of influenza vaccine immunogenicity, including animal and human challenge studies, humoral and cellular immunity parameters, and their potential correlation with real-life protection from disease. Full article

Other

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10 pages, 1924 KiB  
Brief Report
Cross-Reactivity Assessment of Vaccine-Derived SARS-CoV-2 T Cell Responses against BA.2.86 and JN.1
by Muhammad Saqib Sohail, Syed Faraz Ahmed, Ahmed Abdul Quadeer and Matthew R. McKay
Viruses 2024, 16(3), 473; https://doi.org/10.3390/v16030473 - 20 Mar 2024
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Abstract
The SARS-CoV-2 Omicron sub-variants BA.2.86 and JN.1 contain multiple mutations in the spike protein that were not present in previous variants of concern and Omicron sub-variants. Preliminary research suggests that these variants reduce the neutralizing capability of antibodies induced by vaccines, which is [...] Read more.
The SARS-CoV-2 Omicron sub-variants BA.2.86 and JN.1 contain multiple mutations in the spike protein that were not present in previous variants of concern and Omicron sub-variants. Preliminary research suggests that these variants reduce the neutralizing capability of antibodies induced by vaccines, which is particularly significant for JN.1. This raises concern as many widely deployed COVID-19 vaccines are based on the spike protein of the ancestral Wuhan strain of SARS-CoV-2. While T cell responses have been shown to be robust against previous SARS-CoV-2 variants, less is known about the impact of mutations in BA.2.86 and JN.1 on T cell responses. We evaluate the effect of mutations specific to BA.2.86 and JN.1 on experimentally determined T cell epitopes derived from the spike protein of the ancestral Wuhan strain and the spike protein of the XBB.1.5 strain that has been recommended as a booster vaccine. Our data suggest that BA.2.86 and JN.1 affect numerous T cell epitopes in spike compared to previous variants; however, the widespread loss of T cell recognition against these variants is unlikely. Full article
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