Microbial Antigen Delivery 2.0

A special issue of Vaccines (ISSN 2076-393X). This special issue belongs to the section "Vaccine Adjuvants".

Deadline for manuscript submissions: closed (10 July 2021) | Viewed by 3003

Special Issue Editors


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Guest Editor
Department of Poultry Science (Microbiology), North Carolina State University, Raleigh, NC 27695, USA
Interests: microbiology/infectious diseases; salmonella vaccines; synbiotics and immune responses; molecular biology; microbiome; metabolome; free radicals in biology and medicine

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Guest Editor
Etna Biotech S.r.l, Z.I. Blocco Palma I, Stradale V. Lancia, 57, 95121 Catania, Italy
Interests: vaccine; adjuvant; immunology; biotechnology; virosome; antibody; antigens; recombinant proteins; in silico trial

Special Issue Information

Dear Colleagues,

Historical vaccines based on whole microorganisms, either live attenuated or killed, with their successful long track record for safety and efficacy, are considered one of the most important public health interventions to tackle infectious diseases. However, for many pathogens, there are still no vaccines available. Moreover, some of the licensed vaccines show suboptimal efficacy or are not recommended for use in high-risk population groups.

The growing demand for new safer, more efficacious and affordable vaccines has resulted in a shift in research to focus mainly on selected and well characterized antigens and epitopes which are very often low immunogenicity when administered alone. To meet the associated challenges, the knowledge gathered on microbial antigen delivery and their implementation through innovative technologies represent the key points to transforming a low immunogenicity antigen into an efficacious vaccine formulation. Fueled by the recent advances in translational medicine, immunology, molecular biology, bioinformatics, chemistry, and biophysics, innovative delivery systems such as involving recombinant vectors, virus-like particles, nanoparticles, emulsions, and other vehicles have been tailored to elicit a proper and long-lasting host immune response to prevent or to treat the infectious agent. The growing awareness of this aspect is underlined by the increasing numbers of publications.
The aim of this Special Issue is to present novel insights and recent advances in the field of microbial antigen delivery, including discovery, development, manufacturing, and regulatory perspectives on new vaccine formulations.

Prof. Hosni Hassan
Dr. Epifanio Fichera
Guest Editors

Manuscript Submission Information

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Keywords

  • Vaccine
  • Adjuvant
  • Immunogenicity
  • Delivery system
  • Recombinant vaccine
  • Nanoparticles

Published Papers (1 paper)

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Research

16 pages, 1726 KiB  
Article
Attenuated Salmonella enterica Serovar Typhimurium, Strain NC983, Is Immunogenic, and Protective against Virulent Typhimurium Challenges in Mice
by Bryan Troxell, Mary Mendoza, Rizwana Ali, Matthew Koci and Hosni Hassan
Vaccines 2020, 8(4), 646; https://doi.org/10.3390/vaccines8040646 - 03 Nov 2020
Cited by 2 | Viewed by 2480
Abstract
Non-typhoidal Salmonella (NTS) serovars are significant health burden worldwide. Although much effort has been devoted to developing typhoid-based vaccines for humans, currently there is no NTS vaccine available. Presented here is the efficacy of a live attenuated serovar Typhimurium strain (NC983). Oral delivery [...] Read more.
Non-typhoidal Salmonella (NTS) serovars are significant health burden worldwide. Although much effort has been devoted to developing typhoid-based vaccines for humans, currently there is no NTS vaccine available. Presented here is the efficacy of a live attenuated serovar Typhimurium strain (NC983). Oral delivery of strain NC983 was capable of fully protecting C57BL/6 and BALB/c mice against challenge with virulent Typhimurium. Strain NC983 was found to elicit an anti-Typhimurium IgG response following administration of vaccine and boosting doses. Furthermore, in competition experiments with virulent S. Typhimurium (ATCC 14028), NC983 was highly defective in colonization of the murine liver and spleen. Collectively, these results indicate that strain NC983 is a potential live attenuated vaccine strain that warrants further development. Full article
(This article belongs to the Special Issue Microbial Antigen Delivery 2.0)
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