Increased number of tissue factor protein expressing thrombocytes in canine idiopathic immune mediated hemolytic anemia

Publication date

2018-02

Authors

Hennink, ImkeISNI 000000049330001X
van Leeuwen, Martin WISNI 0000000492904997
Penning, Louis CISNI 000000039077188X
Piek, C.J.ISNI 0000000396285460

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Article
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Abstract

Dogs suffering from canine idiopathic immune mediated hemolytic anemia (cIIMHA) are at great risk of dying particularly in the first two weeks after the diagnosis is made. This high mortality risk may be associated with the development of thromboembolism (TE) and/or disseminated intravascular coagulation (DIC) resulting in organ failure. The exact mechanism of the development of TE and/or DIC in cIIMHA is still undetermined. Therefore, this study investigates the presence of tissue factor (TF) in thrombocytes of dogs suffering from cIIMHA, using OptiPrep™ for the isolation of blood cells and immunocytochemistry (ICC) to visualize TF on thrombocytes. The normalised TF quantity, acquired with 'colour deconvolution' (ImageJ plug in), revealed that in cIIMHA dogs the fraction TF positive thrombocytes was statistically significant higher (P < 0.001; mean 0.79; n = 7) compared to the fraction TF positive thrombocytes of the healthy dogs (mean 0.43; n = 9). We further have indications that the fraction of TF positive thrombocytes decreases with time and therapy, but that the progression rate differs individually. Since cIIMHA dogs have more thrombocytes that are TF-positive compared to healthy dogs, this may explain the increased risk to develop TE and DIC. Furthermore, it seems that the number of TF-positive thrombocytes in cIIMHA dogs remains high during the first two weeks of the disease, the time when the animals are at greatest health risk.

Keywords

Journal Article, SDG 3 - Good Health and Well-being

Citation

Hennink, I, van Leeuwen, M W, Penning, L C & Piek, C J 2018, 'Increased number of tissue factor protein expressing thrombocytes in canine idiopathic immune mediated hemolytic anemia', Veterinary Immunology and Immunopathology, vol. 196, pp. 22-29. https://doi.org/10.1016/j.vetimm.2017.12.009