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Assessment of Equine Autoimmune Thrombocytopenia (EAT) by flow cytometry
RATIONALE: Thrombocytopenia is a platelet associated process that occurs in human and animals as result of i) decreased production; ii) increased utilization; iii) increased destruction coupled to the presence of antibodies, within a process know as immune-mediated thrombocytopenia (IMT); or iv) pla...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2001
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC32162/ https://www.ncbi.nlm.nih.gov/pubmed/11313001 http://dx.doi.org/10.1186/1471-2326-1-1 |
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author | Nunez, Rafael Gomes-Keller, M Alice Schwarzwald, Colin Feige, Karsten |
author_facet | Nunez, Rafael Gomes-Keller, M Alice Schwarzwald, Colin Feige, Karsten |
author_sort | Nunez, Rafael |
collection | PubMed |
description | RATIONALE: Thrombocytopenia is a platelet associated process that occurs in human and animals as result of i) decreased production; ii) increased utilization; iii) increased destruction coupled to the presence of antibodies, within a process know as immune-mediated thrombocytopenia (IMT); or iv) platelet sequestration. Thus, the differentiation of the origin of IMT and the development of reliable diagnostic approaches and methodologies are important in the clarification of IMT pathogenesis. Therefore, there is a growing need in the field for easy to perform assays for assessing platelet morphological characteristics paired with detection of platelet-bound IgG. OBJECTIVES: This study is aimed to develop and characterize a single color flow cytometric assay for detection of platelet-bound IgG in horses, in combination with flow cytometric assessment of platelet morphological characteristics. FINDINGS: The FSC and SSC evaluation of the platelets obtained from the thrombocytopenic animals shows several distinctive features in comparison to the flow cytometric profile of platelets from healthy animals. The thrombocytopenic animals displayed i) increased number of platelets with high FSC and high SSC, ii) a significant number of those gigantic platelets had strong fluorescent signal (IgG bound), iii) very small platelets or platelet derived microparticles were found significantly enhanced in one of the thrombocytopenic horses, iv) significant numbers of these microplatelet/microparticles/platelet-fragments still carry very high fluorescence. CONCLUSIONS: This study describes the development and characterization of an easy to perform, inexpensive, and noninvasive single color flow cytometric assay for detection of platelet-bound IgG, in combination with flow cytometric assessment of platelet morphological characteristics in horses. |
format | Text |
id | pubmed-32162 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-321622001-06-01 Assessment of Equine Autoimmune Thrombocytopenia (EAT) by flow cytometry Nunez, Rafael Gomes-Keller, M Alice Schwarzwald, Colin Feige, Karsten BMC Blood Disord Research Article RATIONALE: Thrombocytopenia is a platelet associated process that occurs in human and animals as result of i) decreased production; ii) increased utilization; iii) increased destruction coupled to the presence of antibodies, within a process know as immune-mediated thrombocytopenia (IMT); or iv) platelet sequestration. Thus, the differentiation of the origin of IMT and the development of reliable diagnostic approaches and methodologies are important in the clarification of IMT pathogenesis. Therefore, there is a growing need in the field for easy to perform assays for assessing platelet morphological characteristics paired with detection of platelet-bound IgG. OBJECTIVES: This study is aimed to develop and characterize a single color flow cytometric assay for detection of platelet-bound IgG in horses, in combination with flow cytometric assessment of platelet morphological characteristics. FINDINGS: The FSC and SSC evaluation of the platelets obtained from the thrombocytopenic animals shows several distinctive features in comparison to the flow cytometric profile of platelets from healthy animals. The thrombocytopenic animals displayed i) increased number of platelets with high FSC and high SSC, ii) a significant number of those gigantic platelets had strong fluorescent signal (IgG bound), iii) very small platelets or platelet derived microparticles were found significantly enhanced in one of the thrombocytopenic horses, iv) significant numbers of these microplatelet/microparticles/platelet-fragments still carry very high fluorescence. CONCLUSIONS: This study describes the development and characterization of an easy to perform, inexpensive, and noninvasive single color flow cytometric assay for detection of platelet-bound IgG, in combination with flow cytometric assessment of platelet morphological characteristics in horses. BioMed Central 2001-04-10 /pmc/articles/PMC32162/ /pubmed/11313001 http://dx.doi.org/10.1186/1471-2326-1-1 Text en Copyright © 2001 Nunez et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL. |
spellingShingle | Research Article Nunez, Rafael Gomes-Keller, M Alice Schwarzwald, Colin Feige, Karsten Assessment of Equine Autoimmune Thrombocytopenia (EAT) by flow cytometry |
title | Assessment of Equine Autoimmune Thrombocytopenia (EAT) by flow cytometry |
title_full | Assessment of Equine Autoimmune Thrombocytopenia (EAT) by flow cytometry |
title_fullStr | Assessment of Equine Autoimmune Thrombocytopenia (EAT) by flow cytometry |
title_full_unstemmed | Assessment of Equine Autoimmune Thrombocytopenia (EAT) by flow cytometry |
title_short | Assessment of Equine Autoimmune Thrombocytopenia (EAT) by flow cytometry |
title_sort | assessment of equine autoimmune thrombocytopenia (eat) by flow cytometry |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC32162/ https://www.ncbi.nlm.nih.gov/pubmed/11313001 http://dx.doi.org/10.1186/1471-2326-1-1 |
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