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Protection against feline infectious peritonitis by intranasal inoculation of a temperature-sensitive FIPV vaccine
Cats vaccinated intranasally (i.n.) with a temperature sensitive feline infectious peritonitis virus (ts-FIPV) vaccine were protected against an FIP-inducing challenge. Seventeen of 20 vaccinated cats (85%) survived a rigorous virulent FIPV challenge that caused FIP in 12 of 12 non-vaccinated cats (...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Ltd.
1990
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131383/ https://www.ncbi.nlm.nih.gov/pubmed/2087874 http://dx.doi.org/10.1016/0264-410X(90)90004-6 |
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author | Gerber, J.D. Ingersoll, J.D. Gast, A.M. Christianson, K.K. Selzer, N.L. Landon, R.M. Pfeiffer, N.E. Sharpee, R.L. Beckenhauer, W.H. |
author_facet | Gerber, J.D. Ingersoll, J.D. Gast, A.M. Christianson, K.K. Selzer, N.L. Landon, R.M. Pfeiffer, N.E. Sharpee, R.L. Beckenhauer, W.H. |
author_sort | Gerber, J.D. |
collection | PubMed |
description | Cats vaccinated intranasally (i.n.) with a temperature sensitive feline infectious peritonitis virus (ts-FIPV) vaccine were protected against an FIP-inducing challenge. Seventeen of 20 vaccinated cats (85%) survived a rigorous virulent FIPV challenge that caused FIP in 12 of 12 non-vaccinated cats (100%), 10 (83%) of which died. Intranasal vaccination stimulated serum IgG and serum and salivary IgA antibody responses (measured by ELISA), FIPV-neutralizing antibody (VN), and a cell-mediated immune (CMI) response as measured by lymphocyte proliferation. The serum antibody response to vaccination was not associated with protection. In fact, the IgG, IgA and VN titres were much higher in control cats than in vaccinated cats following challenge suggesting an immune-mediated pathogenesis. In contrast, stimulation of a mucosal IgA response to vaccination was related to protection. The in vitro proliferation of peripheral blood lymphocytes in response to virulent FIPV was observed in vaccinated cats, in vaccinated and challenged cats but not in non-vaccinated challenged cats. |
format | Online Article Text |
id | pubmed-7131383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1990 |
publisher | Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71313832020-04-08 Protection against feline infectious peritonitis by intranasal inoculation of a temperature-sensitive FIPV vaccine Gerber, J.D. Ingersoll, J.D. Gast, A.M. Christianson, K.K. Selzer, N.L. Landon, R.M. Pfeiffer, N.E. Sharpee, R.L. Beckenhauer, W.H. Vaccine Article Cats vaccinated intranasally (i.n.) with a temperature sensitive feline infectious peritonitis virus (ts-FIPV) vaccine were protected against an FIP-inducing challenge. Seventeen of 20 vaccinated cats (85%) survived a rigorous virulent FIPV challenge that caused FIP in 12 of 12 non-vaccinated cats (100%), 10 (83%) of which died. Intranasal vaccination stimulated serum IgG and serum and salivary IgA antibody responses (measured by ELISA), FIPV-neutralizing antibody (VN), and a cell-mediated immune (CMI) response as measured by lymphocyte proliferation. The serum antibody response to vaccination was not associated with protection. In fact, the IgG, IgA and VN titres were much higher in control cats than in vaccinated cats following challenge suggesting an immune-mediated pathogenesis. In contrast, stimulation of a mucosal IgA response to vaccination was related to protection. The in vitro proliferation of peripheral blood lymphocytes in response to virulent FIPV was observed in vaccinated cats, in vaccinated and challenged cats but not in non-vaccinated challenged cats. Published by Elsevier Ltd. 1990-12 2002-11-13 /pmc/articles/PMC7131383/ /pubmed/2087874 http://dx.doi.org/10.1016/0264-410X(90)90004-6 Text en Copyright © 1990 Published by Elsevier Ltd. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Gerber, J.D. Ingersoll, J.D. Gast, A.M. Christianson, K.K. Selzer, N.L. Landon, R.M. Pfeiffer, N.E. Sharpee, R.L. Beckenhauer, W.H. Protection against feline infectious peritonitis by intranasal inoculation of a temperature-sensitive FIPV vaccine |
title | Protection against feline infectious peritonitis by intranasal inoculation of a temperature-sensitive FIPV vaccine |
title_full | Protection against feline infectious peritonitis by intranasal inoculation of a temperature-sensitive FIPV vaccine |
title_fullStr | Protection against feline infectious peritonitis by intranasal inoculation of a temperature-sensitive FIPV vaccine |
title_full_unstemmed | Protection against feline infectious peritonitis by intranasal inoculation of a temperature-sensitive FIPV vaccine |
title_short | Protection against feline infectious peritonitis by intranasal inoculation of a temperature-sensitive FIPV vaccine |
title_sort | protection against feline infectious peritonitis by intranasal inoculation of a temperature-sensitive fipv vaccine |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131383/ https://www.ncbi.nlm.nih.gov/pubmed/2087874 http://dx.doi.org/10.1016/0264-410X(90)90004-6 |
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