Understanding the Pathophysiology of Thrombotic APS through Animal Models

Antiphospholipid syndrome (APS) is a leading acquired cause of thrombotic events, with a notable tendency to promote thrombosis in vascular beds of all sizes, including both arterial and venous circuits. While pathogenic antiphospholipid antibodies circulate at relatively stable levels in blood, thr...

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Main Authors: Alex A. Gandhi, Shanea K. Estes, Christine E. Rysenga, Jason S. Knight
Format: Article
Language:English
Published: MDPI AG 2021-03-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/5/2588
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spelling doaj-404d9d4aef9c4195bdff82f4b3c0ec752021-03-05T00:07:58ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-03-01222588258810.3390/ijms22052588Understanding the Pathophysiology of Thrombotic APS through Animal ModelsAlex A. GandhiShanea K. EstesChristine E. RysengaJason S. Knight0Division of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USAAntiphospholipid syndrome (APS) is a leading acquired cause of thrombotic events, with a notable tendency to promote thrombosis in vascular beds of all sizes, including both arterial and venous circuits. While pathogenic antiphospholipid antibodies circulate at relatively stable levels in blood, thrombosis tends to manifest as discrete and acute events, suggesting the requirement for a “second hit.” While this two-hit model is generally accepted, much remains to be learned about exactly how antiphospholipid antibodies predispose to thrombosis in vivo and exactly how this predisposition interacts with the second hit. To this end, investigators have turned to animal models. Numerous approaches for modeling APS in animals have been described to date, each with potential advantages and disadvantages. This review will attempt to describe the most common APS models employed so far while discussing some pros and cons of each. Mechanisms of thrombotic APS that have thus far been explored in animal models will also be briefly addressed.https://www.mdpi.com/1422-0067/22/5/2588antiphospholipid syndromeantiphospholipid antibodiesthrombosisanimal models
collection DOAJ
language English
format Article
sources DOAJ
author Alex A. Gandhi
Shanea K. Estes
Christine E. Rysenga
Jason S. Knight
spellingShingle Alex A. Gandhi
Shanea K. Estes
Christine E. Rysenga
Jason S. Knight
Understanding the Pathophysiology of Thrombotic APS through Animal Models
International Journal of Molecular Sciences
antiphospholipid syndrome
antiphospholipid antibodies
thrombosis
animal models
author_facet Alex A. Gandhi
Shanea K. Estes
Christine E. Rysenga
Jason S. Knight
author_sort Alex A. Gandhi
title Understanding the Pathophysiology of Thrombotic APS through Animal Models
title_short Understanding the Pathophysiology of Thrombotic APS through Animal Models
title_full Understanding the Pathophysiology of Thrombotic APS through Animal Models
title_fullStr Understanding the Pathophysiology of Thrombotic APS through Animal Models
title_full_unstemmed Understanding the Pathophysiology of Thrombotic APS through Animal Models
title_sort understanding the pathophysiology of thrombotic aps through animal models
publisher MDPI AG
series International Journal of Molecular Sciences
issn 1661-6596
1422-0067
publishDate 2021-03-01
description Antiphospholipid syndrome (APS) is a leading acquired cause of thrombotic events, with a notable tendency to promote thrombosis in vascular beds of all sizes, including both arterial and venous circuits. While pathogenic antiphospholipid antibodies circulate at relatively stable levels in blood, thrombosis tends to manifest as discrete and acute events, suggesting the requirement for a “second hit.” While this two-hit model is generally accepted, much remains to be learned about exactly how antiphospholipid antibodies predispose to thrombosis in vivo and exactly how this predisposition interacts with the second hit. To this end, investigators have turned to animal models. Numerous approaches for modeling APS in animals have been described to date, each with potential advantages and disadvantages. This review will attempt to describe the most common APS models employed so far while discussing some pros and cons of each. Mechanisms of thrombotic APS that have thus far been explored in animal models will also be briefly addressed.
topic antiphospholipid syndrome
antiphospholipid antibodies
thrombosis
animal models
url https://www.mdpi.com/1422-0067/22/5/2588
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