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Platelet-bound antibodies detected by a flow cytometric assay in cats with thrombocytopenia
In cats, primary or secondary immune-mediated thrombocytopenia have rarely been described or characterised. The objective of this study was to determine platelet-bound antibodies (PBA) by a flow cytometric assay in both healthy and thrombocytopenic cats. Direct PBA testing was performed in 42 thromb...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
ESFM and AAFP. Published by Elsevier Ltd.
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129044/ https://www.ncbi.nlm.nih.gov/pubmed/16616569 http://dx.doi.org/10.1016/j.jfms.2006.01.006 |
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author | Kohn, Barbara Linden, Tanja Leibold, Wolfgang |
author_facet | Kohn, Barbara Linden, Tanja Leibold, Wolfgang |
author_sort | Kohn, Barbara |
collection | PubMed |
description | In cats, primary or secondary immune-mediated thrombocytopenia have rarely been described or characterised. The objective of this study was to determine platelet-bound antibodies (PBA) by a flow cytometric assay in both healthy and thrombocytopenic cats. Direct PBA testing was performed in 42 thrombocytopenic cats (platelet counts 6–179 × 10(9)/l, median 56 × 10(9)/l). Of these 42 cats, 19 had positive PBA test results, 17 of which were considered to have secondary immune-mediated thrombocytopenia (sITP). Underlying diseases included fat necroses (four cases), feline infectious peritonitis (three), feline leukaemia virus (two) or feline immunodeficiency virus (two) infections, lymphoma (two), leukaemia (one), hepatitis (one), pyelonephritis (one), or hyperthyroidism (one). In two cats, no underlying disease was found suggesting a primary immune-mediated thrombocytopenia (pITP). The PBA test was negative in 23 cats diagnosed with varying underlying diseases and in 47 healthy control cats with platelet values within the reference range. Only seven of the 42 cats with thrombocytopenia (platelet count 10–57 × 10(9)/l, median 34 × 10(9)/l) had spontaneous bleeding. This study suggests that immune-mediated destruction of platelets might be an important pathological mechanism for feline thrombocytopenia caused by various underlying diseases. In cats, pITP appears to be rarely diagnosed. |
format | Online Article Text |
id | pubmed-7129044 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | ESFM and AAFP. Published by Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71290442020-04-08 Platelet-bound antibodies detected by a flow cytometric assay in cats with thrombocytopenia Kohn, Barbara Linden, Tanja Leibold, Wolfgang J Feline Med Surg Article In cats, primary or secondary immune-mediated thrombocytopenia have rarely been described or characterised. The objective of this study was to determine platelet-bound antibodies (PBA) by a flow cytometric assay in both healthy and thrombocytopenic cats. Direct PBA testing was performed in 42 thrombocytopenic cats (platelet counts 6–179 × 10(9)/l, median 56 × 10(9)/l). Of these 42 cats, 19 had positive PBA test results, 17 of which were considered to have secondary immune-mediated thrombocytopenia (sITP). Underlying diseases included fat necroses (four cases), feline infectious peritonitis (three), feline leukaemia virus (two) or feline immunodeficiency virus (two) infections, lymphoma (two), leukaemia (one), hepatitis (one), pyelonephritis (one), or hyperthyroidism (one). In two cats, no underlying disease was found suggesting a primary immune-mediated thrombocytopenia (pITP). The PBA test was negative in 23 cats diagnosed with varying underlying diseases and in 47 healthy control cats with platelet values within the reference range. Only seven of the 42 cats with thrombocytopenia (platelet count 10–57 × 10(9)/l, median 34 × 10(9)/l) had spontaneous bleeding. This study suggests that immune-mediated destruction of platelets might be an important pathological mechanism for feline thrombocytopenia caused by various underlying diseases. In cats, pITP appears to be rarely diagnosed. ESFM and AAFP. Published by Elsevier Ltd. 2006-08 2006-04-17 /pmc/articles/PMC7129044/ /pubmed/16616569 http://dx.doi.org/10.1016/j.jfms.2006.01.006 Text en Copyright © 2006 ESFM and AAFP. Published by Elsevier Ltd. All rights reserved. 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 Kohn, Barbara Linden, Tanja Leibold, Wolfgang Platelet-bound antibodies detected by a flow cytometric assay in cats with thrombocytopenia |
title | Platelet-bound antibodies detected by a flow cytometric assay in cats with thrombocytopenia |
title_full | Platelet-bound antibodies detected by a flow cytometric assay in cats with thrombocytopenia |
title_fullStr | Platelet-bound antibodies detected by a flow cytometric assay in cats with thrombocytopenia |
title_full_unstemmed | Platelet-bound antibodies detected by a flow cytometric assay in cats with thrombocytopenia |
title_short | Platelet-bound antibodies detected by a flow cytometric assay in cats with thrombocytopenia |
title_sort | platelet-bound antibodies detected by a flow cytometric assay in cats with thrombocytopenia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7129044/ https://www.ncbi.nlm.nih.gov/pubmed/16616569 http://dx.doi.org/10.1016/j.jfms.2006.01.006 |
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