Human multipotent mesenchymal stromal cells in the treatment of postoperative temporal bone defect: an animal model
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378041%3A_____%2F16%3A00450151" target="_blank" >RIV/68378041:_____/16:00450151 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/00216208:11130/16:10320100 RIV/00216208:11150/16:10320100 RIV/00179906:_____/16:10320100
Výsledek na webu
<a href="http://dx.doi.org/10.3727/096368915X689730" target="_blank" >http://dx.doi.org/10.3727/096368915X689730</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.3727/096368915X689730" target="_blank" >10.3727/096368915X689730</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Human multipotent mesenchymal stromal cells in the treatment of postoperative temporal bone defect: an animal model
Popis výsledku v původním jazyce
Canal wall down mastoidectomy is one of the most effective treatments for cholesteatoma. However, it results in anatomical changes in the external and middle ear with a negative impact on the patient's quality of life. To provide complete closure of the mastoid cavity and normalize the anatomy of the middle and external ear, we used human multipotent mesenchymal stromal cells (hMSCs), GMP grade, in a guinea pig model. A method for preparing a biomaterial composed of hMSCs, hydroxyapatite, and tissue glue was developed. Animals from the treated group were implanted with biomaterial composed of hydroxyapatite and hMSCs, while animals in the control group received hydroxyapatite alone. When compared to controls, the group implanted with hMSCs showed a significantly higher ratio of new bone formation (p = 0.00174), as well as a significantly higher volume percentage of new immature bone (p = 0.00166). Our results proved a beneficial effect of hMSCs on temporal bone formation and provided a promising tool to improve the quality of life of patients after canal wall down mastoidectomy by hMSC implantation.
Název v anglickém jazyce
Human multipotent mesenchymal stromal cells in the treatment of postoperative temporal bone defect: an animal model
Popis výsledku anglicky
Canal wall down mastoidectomy is one of the most effective treatments for cholesteatoma. However, it results in anatomical changes in the external and middle ear with a negative impact on the patient's quality of life. To provide complete closure of the mastoid cavity and normalize the anatomy of the middle and external ear, we used human multipotent mesenchymal stromal cells (hMSCs), GMP grade, in a guinea pig model. A method for preparing a biomaterial composed of hMSCs, hydroxyapatite, and tissue glue was developed. Animals from the treated group were implanted with biomaterial composed of hydroxyapatite and hMSCs, while animals in the control group received hydroxyapatite alone. When compared to controls, the group implanted with hMSCs showed a significantly higher ratio of new bone formation (p = 0.00174), as well as a significantly higher volume percentage of new immature bone (p = 0.00166). Our results proved a beneficial effect of hMSCs on temporal bone formation and provided a promising tool to improve the quality of life of patients after canal wall down mastoidectomy by hMSC implantation.
Klasifikace
Druh
J<sub>x</sub> - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)
CEP obor
FP - Ostatní lékařské obory
OECD FORD obor
—
Návaznosti výsledku
Projekt
<a href="/cs/project/LO1309" target="_blank" >LO1309: Buněčná terapie a tkáňové náhrady</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2016
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Cell Transplantation
ISSN
0963-6897
e-ISSN
—
Svazek periodika
25
Číslo periodika v rámci svazku
7
Stát vydavatele periodika
US - Spojené státy americké
Počet stran výsledku
28
Strana od-do
1405-1414
Kód UT WoS článku
000384801200017
EID výsledku v databázi Scopus
2-s2.0-84978134221