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Therapeutic effect of an anti-human-TNF-alpha antibody and itraconazole on feline infectious peritonitis
Feline infectious peritonitis (FIP) is a fatal disease in wild and domestic cat species. Although several drugs are expected to be useful as treatments for FIP, no drugs are available in clinical practice. In this study, we evaluated the therapeutic effect of combined use of adalimumab (an anti-huma...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Vienna
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7110289/ https://www.ncbi.nlm.nih.gov/pubmed/32236683 http://dx.doi.org/10.1007/s00705-020-04605-7 |
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author | Doki, Tomoyoshi Toda, Masahiro Hasegawa, Nobuhisa Hohdatsu, Tsutomu Takano, Tomomi |
author_facet | Doki, Tomoyoshi Toda, Masahiro Hasegawa, Nobuhisa Hohdatsu, Tsutomu Takano, Tomomi |
author_sort | Doki, Tomoyoshi |
collection | PubMed |
description | Feline infectious peritonitis (FIP) is a fatal disease in wild and domestic cat species. Although several drugs are expected to be useful as treatments for FIP, no drugs are available in clinical practice. In this study, we evaluated the therapeutic effect of combined use of adalimumab (an anti-human-TNF-alpha monoclonal antibody, ADA) and itraconazole (ICZ), which are presently available to veterinarians. The neutralizing activity of ADA against fTNF-alpha-induced cytotoxicity was measured in WEHI-164 cells. Ten specific pathogen-free (SPF) cats were inoculated intraperitoneally with type I FIPV KU-2. To the cats that developed FIP, ADA (10 mg/animal) was administered twice between day 0 and day 4 after the start of treatment. ICZ (50 mg/head, SID) was orally administered daily from day 0 after the start of treatment. ADA demonstrated dose-dependent neutralizing activity against rfTNF-alpha. In an animal experiment, 2 of 3 cats showed improvements in FIP clinical symptoms and blood chemistry test results, an increase in the peripheral blood lymphocyte count, and a decrease in the plasma alpha 1-AGP level were observed after the beginning of treatment. One of the cats failed to respond to treatment and was euthanized, although the viral gene level in ascites temporarily decreased after the start of treatment. ADA was found to have neutralizing activity against rfTNF-alpha. The combined use of ADA and ICZ showed a therapeutic effect for experimentally induced FIP. We consider these drugs to be a treatment option until effective anti-FIPV drugs become available. |
format | Online Article Text |
id | pubmed-7110289 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-71102892020-04-01 Therapeutic effect of an anti-human-TNF-alpha antibody and itraconazole on feline infectious peritonitis Doki, Tomoyoshi Toda, Masahiro Hasegawa, Nobuhisa Hohdatsu, Tsutomu Takano, Tomomi Arch Virol Original Article Feline infectious peritonitis (FIP) is a fatal disease in wild and domestic cat species. Although several drugs are expected to be useful as treatments for FIP, no drugs are available in clinical practice. In this study, we evaluated the therapeutic effect of combined use of adalimumab (an anti-human-TNF-alpha monoclonal antibody, ADA) and itraconazole (ICZ), which are presently available to veterinarians. The neutralizing activity of ADA against fTNF-alpha-induced cytotoxicity was measured in WEHI-164 cells. Ten specific pathogen-free (SPF) cats were inoculated intraperitoneally with type I FIPV KU-2. To the cats that developed FIP, ADA (10 mg/animal) was administered twice between day 0 and day 4 after the start of treatment. ICZ (50 mg/head, SID) was orally administered daily from day 0 after the start of treatment. ADA demonstrated dose-dependent neutralizing activity against rfTNF-alpha. In an animal experiment, 2 of 3 cats showed improvements in FIP clinical symptoms and blood chemistry test results, an increase in the peripheral blood lymphocyte count, and a decrease in the plasma alpha 1-AGP level were observed after the beginning of treatment. One of the cats failed to respond to treatment and was euthanized, although the viral gene level in ascites temporarily decreased after the start of treatment. ADA was found to have neutralizing activity against rfTNF-alpha. The combined use of ADA and ICZ showed a therapeutic effect for experimentally induced FIP. We consider these drugs to be a treatment option until effective anti-FIPV drugs become available. Springer Vienna 2020-03-31 2020 /pmc/articles/PMC7110289/ /pubmed/32236683 http://dx.doi.org/10.1007/s00705-020-04605-7 Text en © Springer-Verlag GmbH Austria, part of Springer Nature 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Doki, Tomoyoshi Toda, Masahiro Hasegawa, Nobuhisa Hohdatsu, Tsutomu Takano, Tomomi Therapeutic effect of an anti-human-TNF-alpha antibody and itraconazole on feline infectious peritonitis |
title | Therapeutic effect of an anti-human-TNF-alpha antibody and itraconazole on feline infectious peritonitis |
title_full | Therapeutic effect of an anti-human-TNF-alpha antibody and itraconazole on feline infectious peritonitis |
title_fullStr | Therapeutic effect of an anti-human-TNF-alpha antibody and itraconazole on feline infectious peritonitis |
title_full_unstemmed | Therapeutic effect of an anti-human-TNF-alpha antibody and itraconazole on feline infectious peritonitis |
title_short | Therapeutic effect of an anti-human-TNF-alpha antibody and itraconazole on feline infectious peritonitis |
title_sort | therapeutic effect of an anti-human-tnf-alpha antibody and itraconazole on feline infectious peritonitis |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7110289/ https://www.ncbi.nlm.nih.gov/pubmed/32236683 http://dx.doi.org/10.1007/s00705-020-04605-7 |
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