Mathieu Spriet

Dr. Mathieu Spriet

orcid

Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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14 September 2018 in Equine Veterinary Journal
Verified
Journal Article
Closed access
PDF file
MSMathieu Spriet
Mathieu Spriet
PEP. Espinosa‐Mur
P. Espinosa‐Mur
DCD. D. Cissell
D. D. Cissell
KPK. L. Phillips
K. L. Phillips
GAG. Arino‐Estrada
G. Arino‐Estrada
SSS. M. Stover
S. M. Stover

30 December 2011 in Equine Veterinary Journal
Verified
Journal Article
Closed access
PDF file
AGAlbert Sole Guitart
Albert Sole Guitart
MSMathieu Spriet
Mathieu Spriet
LGL. D. Galuppo
L. D. Galuppo
KPK. A. Padgett
K. A. Padgett
DBD. L. Borjesson
D. L. Borjesson
MVM. A. Vidal
M. A. Vidal

25 February 2016 in Veterinary Radiology & Ultrasound
Verified
Journal Article
Closed access
PDF file
ADAnthony DeRouen
Anthony DeRouen
MSMathieu Spriet
Mathieu Spriet
MAMonica Aleman
Monica Aleman

10 April 2018 in Stem Cell Research & Therapy
Verified
Journal Article
Open access
PDF file
DBDanielle Jaqueta Barberini
Danielle Jaqueta Barberini
MAMonica Aleman
Monica Aleman
FAFabio Aristizabal
Fabio Aristizabal
MSMathieu Spriet
Mathieu Spriet
KCKaitlin Clark
Kaitlin Clark
DBDori L. Borjesson
Dori L. Borjesson
It is currently unknown if the intrathecal administration of a high dose of allogeneic mesenchymal stem cells (MSCs) is safe, how MSCs migrate throughout the vertebral canal after intrathecal administration, and whether MSCs are able to home to a site of injury. The aims of the study were: 1) to evaluate the safety of intrathecal injection of 100 million allogeneic adipose-derived MSCs (ASCs); 2) to assess the distribution of ASCs after atlanto-occipital (AO) and lumbosacral (LS) injection in healthy horses; and 3) to determine if ASCs homed to the site of injury in neurologically diseased horses. Six healthy horses received 100 × 106 allogeneic ASCs via AO (n = 3) or LS injection (n = 3). For two of these horses, ASCs were radiolabeled with technetium and injected AO (n = 1) or LS (n = 1). Neurological examinations were performed daily, and blood and cerebrospinal fluid (CSF) were evaluated prior to and at 30 days after injection. Scintigraphic images were obtained immediately postinjection and at 30 mins, 1 h, 5 h, and 24 h after injection. Three horses with cervical vertebral compressive myelopathy (CVCM) received 100 × 106 allogeneic ASCs labeled with green fluorescent protein (GFP) via AO injection and were euthanized 1–2 weeks after injection for a full nervous system necropsy. CSF parameters were compared using a paired student’s t test. There were no significant alterations in blood, CSF, or neurological examinations at any point after either AO or LS ASC injections into healthy horses. The radioactive signal could be identified all the way to the lumbar area after AO ASC injection. After LS injection, the signal extended caudally but only a minimal radioactive signal extended further cranially. GFP-labeled ASCs were not present at the site of disease at either 1 or 2 weeks following intrathecal administration. The intrathecal injection of allogeneic ASCs was safe and easy to perform in horses. The AO administration of ASCs resulted in better distribution within the entire subarachnoid space in healthy horses. ASCs could not be found after 7 or 15 days of injection at the site of injury in horses with CVCM.

10 November 2020 in Equine Veterinary Journal
Verified
Journal Article
Closed access
PDF file
PEPablo Espinosa‐Mur
Pablo Espinosa‐Mur
KPKathryn L. Phillips
Kathryn L. Phillips
LGLarry D. Galuppo
Larry D. Galuppo
ADAnthony DeRouen
Anthony DeRouen
PBPhilippe Benoit
Philippe Benoit
MSMathieu Spriet
Mathieu Spriet

18 August 2017 in Equine Veterinary Journal
Verified
Journal Article
Closed access
PDF file
MSMathieu Spriet
Mathieu Spriet
PEP. Espinosa
P. Espinosa
AKA. Z. Kyme
A. Z. Kyme
KPK. L. Phillips
K. L. Phillips
SKS. A. Katzman
S. A. Katzman
DBD. Beylin
D. Beylin