Rabies Vaccination and Immunotherapy

A special issue of Vaccines (ISSN 2076-393X). This special issue belongs to the section "Vaccines against Infectious Diseases".

Deadline for manuscript submissions: closed (20 August 2022) | Viewed by 4184

Special Issue Editor


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Guest Editor
The Laboratory of Immunology, The Wadsworth Center, New York State Department of Health, Albany, NY 12201-2002, USA
Interests: rabies virus; immunopathology; immune evasion; vaccines; antibodies; antivirals
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Special Issue Information

Dear Colleagues,

Although rabies virus is nearly 100% fatal once clinical signs develop, it is also a vaccine-preventable disease. However, multiple factors have impeded successful and widespread administration of rabies vaccines and immunotherapies, including expense and the need for cold chain storage in areas that are remote and may lack reliable electricity. Additionally, vaccines and immunotherapies for rabies virus need to demonstrate high efficacy given the potential for a fatal outcome in untreated or inadequately treated individuals exposed to rabies virus.

The goal of this Special Issue is to feature manuscripts addressing the advancements in the treatment and prevention of rabies infection, including but not limited to developing effective rabies vaccines, novel therapeutics, antiviral response, animal models, and delivery methods. Research articles that describe prevention and potential treatment for lyssavirus phylogroups II and III are also welcome.

Dr. April D. Davis
Guest Editor

Manuscript Submission Information

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Keywords

  • Rabies
  • Vaccine
  • Antibodies
  • Post-exposure prophylaxis
  • Host response
  • Animal model

Published Papers (1 paper)

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Research

14 pages, 2532 KiB  
Article
Comparable Long-Term Rabies Immunity in Foxes after IntraMuscular and Oral Application Using a Third-Generation Oral Rabies Virus Vaccine
by Verena te Kamp, Virginia Friedrichs, Conrad M. Freuling, Ad Vos, Madlin Potratz, Antonia Klein, Luca M. Zaeck, Elisa Eggerbauer, Peter Schuster, Christian Kaiser, Steffen Ortmann, Antje Kretzschmar, Katharina Bobe, Michael R. Knittler, Anca Dorhoi, Stefan Finke and Thomas Müller
Vaccines 2021, 9(1), 49; https://doi.org/10.3390/vaccines9010049 - 14 Jan 2021
Cited by 4 | Viewed by 3206
Abstract
The live genetically-engineered oral rabies virus (RABV) variant SPBN GASGAS induces long-lasting immunity in foxes and protection against challenge with an otherwise lethal dose of RABV field strains both after experimental oral and parenteral routes of administration. Induction of RABV-specific binding antibodies and [...] Read more.
The live genetically-engineered oral rabies virus (RABV) variant SPBN GASGAS induces long-lasting immunity in foxes and protection against challenge with an otherwise lethal dose of RABV field strains both after experimental oral and parenteral routes of administration. Induction of RABV-specific binding antibodies and immunoglobulin isotypes (IgM, total IgG, IgG1, IgG2) were comparable in orally and parenterally vaccinated foxes. Differences were only observed in the induction of virus-neutralizing (VNA) titers, which were significantly higher in the parenterally vaccinated group. The dynamics of rabies-specific antibodies pre- and post-challenge (365 days post vaccination) suggest the predominance of type-1 immunity protection of SPBN GASGAS. Independent of the route of administration, in the absence of IgG1 the immune response to SPBN GAGAS was mainly IgG2 driven. Interestingly, vaccination with SPBN GASGAS does not cause significant differences in inducible IFN-γ production in vaccinated animals, indicating a relatively weak cellular immune response during challenge. Notably, the parenteral application of SPBN GASGAS did not induce any adverse side effects in foxes, thus supporting safety studies of this oral rabies vaccine in various species. Full article
(This article belongs to the Special Issue Rabies Vaccination and Immunotherapy)
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