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Neutrophil Extracellular Traps in Plasma from Dogs with Immune‐mediated Hemolytic Anemia
BACKGROUND: Neutrophil extracellular traps (NETs) are part of the innate immune response and are essential in local pathogen control, but are associated with pathological inflammation, organ damage, autoimmunity, and thrombosis. Immune‐mediated hemolytic anemia (IMHA) is a pro‐inflammatory, prothrom...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787156/ https://www.ncbi.nlm.nih.gov/pubmed/29214674 http://dx.doi.org/10.1111/jvim.14881 |
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author | Lawson, C. Smith, S.A. O'Brien, M. McMichael, M. |
author_facet | Lawson, C. Smith, S.A. O'Brien, M. McMichael, M. |
author_sort | Lawson, C. |
collection | PubMed |
description | BACKGROUND: Neutrophil extracellular traps (NETs) are part of the innate immune response and are essential in local pathogen control, but are associated with pathological inflammation, organ damage, autoimmunity, and thrombosis. Immune‐mediated hemolytic anemia (IMHA) is a pro‐inflammatory, prothrombotic disease associated with high mortality. HYPOTHESIS/OBJECTIVES: Neutrophil extracellular traps (NETs) are a feature of the inflammatory process in dogs with IMHA. The objective of the study was to evaluate plasma from dogs with IMHA for the presence of 2 indirect markers and 1 direct marker of NETs. ANIMALS: Healthy client‐owned dogs (56) and hospitalized dogs with IMHA (n = 35). METHODS: Prospective study. Plasma samples for all dogs were evaluated for cell‐free DNA using a fluorescence assay, histone‐DNA (hisDNA) complex using an ELISA, and citrullinated histone H3 (specific for NETosis) using Western blot. Reference intervals were generated using plasma from healthy dogs. RESULTS: In dogs with IMHA, cell‐free DNA concentration was above the reference interval in 17% of samples with a median (range) of 1.0 μg/mL (0.1–17.3), and hisDNA concentration was above the reference interval in 94% of samples with a median (range) of 30.7 × pooled normal plasma (PNP; 0.6–372.1). Western blot for citrullinated histone H3 identified detectable bands in 84% samples from dogs with IMHA. CONCLUSIONS AND CLINICAL IMPORTANCE: The assay for cell‐free DNA detected evidence of NETs in fewer dogs than did the other approaches. Excessive NETs appears to be a feature of IMHA in dogs and contributions to the prothrombotic state deserve further study. |
format | Online Article Text |
id | pubmed-5787156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57871562018-02-08 Neutrophil Extracellular Traps in Plasma from Dogs with Immune‐mediated Hemolytic Anemia Lawson, C. Smith, S.A. O'Brien, M. McMichael, M. J Vet Intern Med SMALL ANIMAL BACKGROUND: Neutrophil extracellular traps (NETs) are part of the innate immune response and are essential in local pathogen control, but are associated with pathological inflammation, organ damage, autoimmunity, and thrombosis. Immune‐mediated hemolytic anemia (IMHA) is a pro‐inflammatory, prothrombotic disease associated with high mortality. HYPOTHESIS/OBJECTIVES: Neutrophil extracellular traps (NETs) are a feature of the inflammatory process in dogs with IMHA. The objective of the study was to evaluate plasma from dogs with IMHA for the presence of 2 indirect markers and 1 direct marker of NETs. ANIMALS: Healthy client‐owned dogs (56) and hospitalized dogs with IMHA (n = 35). METHODS: Prospective study. Plasma samples for all dogs were evaluated for cell‐free DNA using a fluorescence assay, histone‐DNA (hisDNA) complex using an ELISA, and citrullinated histone H3 (specific for NETosis) using Western blot. Reference intervals were generated using plasma from healthy dogs. RESULTS: In dogs with IMHA, cell‐free DNA concentration was above the reference interval in 17% of samples with a median (range) of 1.0 μg/mL (0.1–17.3), and hisDNA concentration was above the reference interval in 94% of samples with a median (range) of 30.7 × pooled normal plasma (PNP; 0.6–372.1). Western blot for citrullinated histone H3 identified detectable bands in 84% samples from dogs with IMHA. CONCLUSIONS AND CLINICAL IMPORTANCE: The assay for cell‐free DNA detected evidence of NETs in fewer dogs than did the other approaches. Excessive NETs appears to be a feature of IMHA in dogs and contributions to the prothrombotic state deserve further study. John Wiley and Sons Inc. 2017-12-07 2018 /pmc/articles/PMC5787156/ /pubmed/29214674 http://dx.doi.org/10.1111/jvim.14881 Text en Copyright © 2017 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) 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 | SMALL ANIMAL Lawson, C. Smith, S.A. O'Brien, M. McMichael, M. Neutrophil Extracellular Traps in Plasma from Dogs with Immune‐mediated Hemolytic Anemia |
title | Neutrophil Extracellular Traps in Plasma from Dogs with Immune‐mediated Hemolytic Anemia |
title_full | Neutrophil Extracellular Traps in Plasma from Dogs with Immune‐mediated Hemolytic Anemia |
title_fullStr | Neutrophil Extracellular Traps in Plasma from Dogs with Immune‐mediated Hemolytic Anemia |
title_full_unstemmed | Neutrophil Extracellular Traps in Plasma from Dogs with Immune‐mediated Hemolytic Anemia |
title_short | Neutrophil Extracellular Traps in Plasma from Dogs with Immune‐mediated Hemolytic Anemia |
title_sort | neutrophil extracellular traps in plasma from dogs with immune‐mediated hemolytic anemia |
topic | SMALL ANIMAL |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5787156/ https://www.ncbi.nlm.nih.gov/pubmed/29214674 http://dx.doi.org/10.1111/jvim.14881 |
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