Detection and dynamics of anti-platelet antibodies in thrombocytopenic dogs with and without idiopathic immune thrombocytopenia.


Journal

Journal of veterinary internal medicine
ISSN: 1939-1676
Titre abrégé: J Vet Intern Med
Pays: United States
ID NLM: 8708660

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 06 03 2019
accepted: 05 02 2020
pubmed: 20 2 2020
medline: 15 12 2020
entrez: 20 2 2020
Statut: ppublish

Résumé

Antiplatelet antibodies are detected in multiple diseases including primary immune thrombocytopenia (ITP). Dynamics of how these antibodies change over time in ITP is unknown in dogs. Antiplatelet antibodies (APA) will be detected in thrombocytopenic dogs with multiple etiologies and dynamics of APA in dogs with ITP can be used to evaluate response to treatment and relapse. Determine APA at the time of diagnosis in thrombocytopenic dogs and serially in primary ITP dogs. Seventy-nine thrombocytopenic dogs and 28 primary ITP dogs. Direct flow cytometry was performed in thrombocytopenic dogs at initial evaluation and serially in suspected primary ITP dogs. In primary ITP dogs, a 2-tailed Fisher's exact test was performed comparing survival to discharge between dogs with and without melena and to relate response to treatment and relapse to changes in APA and platelet count (repeated measures analysis, Spearman correlation). Twenty percent (16/79) of thrombocytopenic non-ITP dogs with infectious, neoplastic, or other diseases and all primary ITP dogs were positive for APA. Melena at initial evaluation was associated with decreased survival to discharge (odds ratio 0.06; P = .01). Persistence of APA was not associated with response to treatment, but recurrence of antibodies was associated with relapse (odds ratio 205.0; P < .01). There was no difference in percentage of APA or platelet count at initial diagnosis between dogs that did or did not respond to treatment. Serial monitoring of APA in dogs with primary ITP appeared beneficial for determining relapse of disease.

Sections du résumé

BACKGROUND BACKGROUND
Antiplatelet antibodies are detected in multiple diseases including primary immune thrombocytopenia (ITP). Dynamics of how these antibodies change over time in ITP is unknown in dogs.
HYPOTHESIS/OBJECTIVES OBJECTIVE
Antiplatelet antibodies (APA) will be detected in thrombocytopenic dogs with multiple etiologies and dynamics of APA in dogs with ITP can be used to evaluate response to treatment and relapse. Determine APA at the time of diagnosis in thrombocytopenic dogs and serially in primary ITP dogs.
ANIMALS METHODS
Seventy-nine thrombocytopenic dogs and 28 primary ITP dogs.
METHODS METHODS
Direct flow cytometry was performed in thrombocytopenic dogs at initial evaluation and serially in suspected primary ITP dogs. In primary ITP dogs, a 2-tailed Fisher's exact test was performed comparing survival to discharge between dogs with and without melena and to relate response to treatment and relapse to changes in APA and platelet count (repeated measures analysis, Spearman correlation).
RESULTS RESULTS
Twenty percent (16/79) of thrombocytopenic non-ITP dogs with infectious, neoplastic, or other diseases and all primary ITP dogs were positive for APA. Melena at initial evaluation was associated with decreased survival to discharge (odds ratio 0.06; P = .01). Persistence of APA was not associated with response to treatment, but recurrence of antibodies was associated with relapse (odds ratio 205.0; P < .01). There was no difference in percentage of APA or platelet count at initial diagnosis between dogs that did or did not respond to treatment.
CONCLUSIONS AND CLINICAL IMPORTANCE CONCLUSIONS
Serial monitoring of APA in dogs with primary ITP appeared beneficial for determining relapse of disease.

Identifiants

pubmed: 32072705
doi: 10.1111/jvim.15737
pmc: PMC7096660
doi:

Substances chimiques

Autoantibodies 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

700-709

Subventions

Organisme : Center for Companion Animal Studies

Informations de copyright

© 2020 The Authors. Journal of Veterinary Internal Medicine published by Wiley Periodicals, Inc. on behalf of the American College of Veterinary Internal Medicine.

Références

J Am Vet Med Assoc. 2009 Oct 15;235(8):960-6
pubmed: 19827982
Blood. 2017 Jun 22;129(25):3389-3391
pubmed: 28468795
Vet Immunol Immunopathol. 2000 Nov 23;77(1-2):145-50
pubmed: 11068072
Am J Vet Res. 2002 Jan;63(1):124-9
pubmed: 16206793
Autoimmun Rev. 2017 Jun;16(6):620-632
pubmed: 28428120
J Small Anim Pract. 2008 Oct;49(10):518-24
pubmed: 18793252
Eur J Haematol. 2006 May;76(5):427-31
pubmed: 16480433
Vet Anaesth Analg. 2012 Mar;39(2):206-17
pubmed: 22248445
Vet Clin Pathol. 1986;15(4):13-7
pubmed: 15334363
J Vet Intern Med. 1994 Jan-Feb;8(1):36-9
pubmed: 8176661
Vet Immunol Immunopathol. 1996 May;51(1-2):13-20
pubmed: 8797272
J Am Vet Med Assoc. 2011 Feb 1;238(3):346-52
pubmed: 21281218
Am J Vet Res. 1994 Aug;55(8):1111-4
pubmed: 7978651
Blood. 2010 Feb 11;115(6):1247-53
pubmed: 20007808
J Am Vet Med Assoc. 1995 Feb 1;206(3):332-4
pubmed: 7751241
J Am Vet Med Assoc. 1995 Jan 1;206(1):47-52
pubmed: 7744662
Blood. 2014 Nov 20;124(22):3316-9
pubmed: 25298039
Vet Clin Pathol. 2001;30(3):141-149
pubmed: 12024314
Br J Haematol. 2017 Jul;178(2):302-307
pubmed: 28444742
Vet Immunol Immunopathol. 2006 Apr 15;110(3-4):331-7
pubmed: 16406554
Vet Immunol Immunopathol. 2018 Aug;202:109-114
pubmed: 30078583
Blood. 2010 Jan 14;115(2):168-86
pubmed: 19846889
Hematol Oncol Clin North Am. 2007 Aug;21(4):685-96, vi
pubmed: 17666285
Vet J. 2011 Apr;188(1):118-21
pubmed: 20456989
Blood. 2004 Jun 15;103(12):4562-4
pubmed: 14976036
Vet Clin North Am Small Anim Pract. 2012 Mar;42(2):289-306, vi-vii
pubmed: 22381180
Am J Vet Res. 1995 Dec;56(12):1555-8
pubmed: 8599513
J Thromb Haemost. 2012 Apr;10(4):695-7
pubmed: 22332994
Nat Med. 2003 Sep;9(9):1123-4
pubmed: 12937414
Immunohematology. 2014;30(2):55-65
pubmed: 25247620
Vet Clin Pathol. 2015 Sep;44(3):355-68
pubmed: 26302235
J Am Anim Hosp Assoc. 1999 Jan-Feb;35(1):56-61
pubmed: 9934930
Int J Lab Hematol. 2008 Feb;30(1):58-64
pubmed: 18190469
J Vet Intern Med. 2020 Mar;34(2):700-709
pubmed: 32072705
J Vet Intern Med. 2014 Sep-Oct;28(5):1575-9
pubmed: 25056453
Sci Rep. 2016 Jun 20;6:27445
pubmed: 27321376
Crit Rev Clin Lab Sci. 2016 Dec;53(6):409-30
pubmed: 27282765
J Vet Emerg Crit Care (San Antonio). 2017 Sep;27(5):569-578
pubmed: 28749085
Vet Immunol Immunopathol. 1995 Sep;48(1-2):177-82
pubmed: 8533312

Auteurs

Sarah Shropshire (S)

Colorado State University, Fort Collins, Colorado.

Steven Dow (S)

Colorado State University, Fort Collins, Colorado.

Michael Lappin (M)

Colorado State University, Fort Collins, Colorado.

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Classifications MeSH