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Survival of rabid rabbits after intrathecal immunization
Rabies is a fatal zoonotic disease for which no effective treatment measures are currently available. Rabies virus (RABV) has anti-apoptotic and anti-inflammatory properties that suppress nerve cell damage and inflammation in the CNS. These features imply that the elimination of RABV from the CNS by...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235457/ https://www.ncbi.nlm.nih.gov/pubmed/24397792 http://dx.doi.org/10.1111/neup.12094 |
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author | Kesdangsakonwut, Sawang Sunden, Yuji Aoshima, Keisuke Iwaki, Yoshimi Okumura, Masahiro Sawa, Hirofumi Umemura, Takashi |
author_facet | Kesdangsakonwut, Sawang Sunden, Yuji Aoshima, Keisuke Iwaki, Yoshimi Okumura, Masahiro Sawa, Hirofumi Umemura, Takashi |
author_sort | Kesdangsakonwut, Sawang |
collection | PubMed |
description | Rabies is a fatal zoonotic disease for which no effective treatment measures are currently available. Rabies virus (RABV) has anti-apoptotic and anti-inflammatory properties that suppress nerve cell damage and inflammation in the CNS. These features imply that the elimination of RABV from the CNS by appropriate treatment could lead to complete recovery from rabies. Ten rabbits showing neuromuscular symptoms of rabies after subcutaneous (SC) immunization using commercially available vaccine containing inactivated whole RABV particles and subsequent fixed RABV (CVS strain) inoculation into hind limb muscles were allocated into three groups. Three rabbits received no further treatment (the SC group), three rabbits received three additional SC immunizations using the same vaccine, and four rabbits received three intrathecal (IT) immunizations, in which the vaccine was inoculated directly into the cerebrospinal fluid (the SC/IT group). An additional three naïve rabbits were inoculated intramuscularly with RABV and not vaccinated. The rabbits exhibited neuromuscular symptoms of rabies within 4–8 days post-inoculation (dpi) of RABV. All of the rabbits died within 8–12 dpi with the exception of one rabbit in the SC group and all four rabbits in SC/IT group, which recovered and started to respond to external stimuli at 11–18 dpi and survived until the end of the experimental period. RABV was eliminated from the CNS of the surviving rabbits. We report here a possible, although still incomplete, therapy for rabies using IT immunization. Our protocol may rescue the life of rabid patients and prompt the future development of novel therapies against rabies. |
format | Online Article Text |
id | pubmed-4235457 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-42354572014-12-19 Survival of rabid rabbits after intrathecal immunization Kesdangsakonwut, Sawang Sunden, Yuji Aoshima, Keisuke Iwaki, Yoshimi Okumura, Masahiro Sawa, Hirofumi Umemura, Takashi Neuropathology Original Articles Rabies is a fatal zoonotic disease for which no effective treatment measures are currently available. Rabies virus (RABV) has anti-apoptotic and anti-inflammatory properties that suppress nerve cell damage and inflammation in the CNS. These features imply that the elimination of RABV from the CNS by appropriate treatment could lead to complete recovery from rabies. Ten rabbits showing neuromuscular symptoms of rabies after subcutaneous (SC) immunization using commercially available vaccine containing inactivated whole RABV particles and subsequent fixed RABV (CVS strain) inoculation into hind limb muscles were allocated into three groups. Three rabbits received no further treatment (the SC group), three rabbits received three additional SC immunizations using the same vaccine, and four rabbits received three intrathecal (IT) immunizations, in which the vaccine was inoculated directly into the cerebrospinal fluid (the SC/IT group). An additional three naïve rabbits were inoculated intramuscularly with RABV and not vaccinated. The rabbits exhibited neuromuscular symptoms of rabies within 4–8 days post-inoculation (dpi) of RABV. All of the rabbits died within 8–12 dpi with the exception of one rabbit in the SC group and all four rabbits in SC/IT group, which recovered and started to respond to external stimuli at 11–18 dpi and survived until the end of the experimental period. RABV was eliminated from the CNS of the surviving rabbits. We report here a possible, although still incomplete, therapy for rabies using IT immunization. Our protocol may rescue the life of rabid patients and prompt the future development of novel therapies against rabies. BlackWell Publishing Ltd 2014-06 2014-01-07 /pmc/articles/PMC4235457/ /pubmed/24397792 http://dx.doi.org/10.1111/neup.12094 Text en © 2014 The Authors. Neuropathology published by Wiley Publishing Asia Pty Ltd on behalf of Japanese Society of Neuropathology. http://creativecommons.org/licenses/by-nc/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Original Articles Kesdangsakonwut, Sawang Sunden, Yuji Aoshima, Keisuke Iwaki, Yoshimi Okumura, Masahiro Sawa, Hirofumi Umemura, Takashi Survival of rabid rabbits after intrathecal immunization |
title | Survival of rabid rabbits after intrathecal immunization |
title_full | Survival of rabid rabbits after intrathecal immunization |
title_fullStr | Survival of rabid rabbits after intrathecal immunization |
title_full_unstemmed | Survival of rabid rabbits after intrathecal immunization |
title_short | Survival of rabid rabbits after intrathecal immunization |
title_sort | survival of rabid rabbits after intrathecal immunization |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4235457/ https://www.ncbi.nlm.nih.gov/pubmed/24397792 http://dx.doi.org/10.1111/neup.12094 |
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