-
Je něco špatně v tomto záznamu ?
Efficacy and safety of human mesenchymal stromal cells in healing of critical-size bone defects in immunodeficient rats
R. Pytlík, C. Rentsch, T. Soukup, L. Novotný, B. Rentsch, V. Kanderová, H. Rychtrmocová, M. Kalmárová, D. Stehlík, M. Trněný, O. Slanař
Jazyk angličtina Země Česko
Typ dokumentu časopisecké články
Grantová podpora
NT13531
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Zdroj
NLK
Directory of Open Access Journals
od 1991
Free Medical Journals
od 1998
ProQuest Central
od 2005-01-01
Medline Complete (EBSCOhost)
od 2006-01-01
Nursing & Allied Health Database (ProQuest)
od 2005-01-01
Health & Medicine (ProQuest)
od 2005-01-01
ROAD: Directory of Open Access Scholarly Resources
od 1998
- MeSH
- dospělí MeSH
- femur diagnostické zobrazování fyziologie MeSH
- hojení ran fyziologie MeSH
- krysa rodu rattus MeSH
- lidé středního věku MeSH
- lidé MeSH
- mezenchymální kmenové buňky fyziologie MeSH
- náhodné rozdělení MeSH
- osteogeneze fyziologie MeSH
- počítačová rentgenová tomografie metody MeSH
- potkani nazí MeSH
- senioři MeSH
- syndromy imunologické nedostatečnosti diagnostické zobrazování imunologie terapie MeSH
- transplantace mezenchymálních kmenových buněk metody MeSH
- výsledek terapie MeSH
- zvířata MeSH
- Check Tag
- dospělí MeSH
- krysa rodu rattus MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
To evaluate the preclinical efficacy and safety of human mesenchymal stem cells (hMSC) rapidly expanded in growth medium for clinical use with human serum and recombinant growth factors, we conducted a controlled, randomized trial of plasma clots with hMSC vs. plasma clots only in critical segmental femoral defects in rnu/rnu immunodeficient rats. X-ray, microCT and histomorphometrical evaluation were performed at 8 and 16 weeks. MSC were obtained from healthy volunteers and patients with lymphoid malignancy. Human MSC survived in the defect for the entire duration of the trial. MSC from healthy volunteers, in contrast to hMSC from cancer patients, significantly improved bone healing at 8, but not 16 weeks. However, at 16 weeks, hMSC significantly improved vasculogenesis in residual defect. We conclude that hMSC from healthy donors significantly contributed to the healing of bone defects at 8 weeks and to the vascularisation of residual connective tissue for up to 16 weeks. We found the administration of hMSC to be safe, as no adverse reaction to human cells at the site of implantation and no evidence of migration of hMSC to distant organs was detected.
Finn Pathologists One Eyed Lane Weybread Norfolk IP21 5TT United Kingdom
Institute of Anatomy 1st Medical Faculty Charles University Prague Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc17026019
- 003
- CZ-PrNML
- 005
- 20190514105832.0
- 007
- ta
- 008
- 170824s2017 xr ad f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.33549/physiolres.933376 $2 doi
- 035 __
- $a (PubMed)27782744
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Pytlík, Robert, $u First Department of Medicine, First Medical Faculty, Charles University, Prague and General University Hospital, Prague, Czech Republic $d 1967- $7 xx0061345
- 245 10
- $a Efficacy and safety of human mesenchymal stromal cells in healing of critical-size bone defects in immunodeficient rats / $c R. Pytlík, C. Rentsch, T. Soukup, L. Novotný, B. Rentsch, V. Kanderová, H. Rychtrmocová, M. Kalmárová, D. Stehlík, M. Trněný, O. Slanař
- 520 9_
- $a To evaluate the preclinical efficacy and safety of human mesenchymal stem cells (hMSC) rapidly expanded in growth medium for clinical use with human serum and recombinant growth factors, we conducted a controlled, randomized trial of plasma clots with hMSC vs. plasma clots only in critical segmental femoral defects in rnu/rnu immunodeficient rats. X-ray, microCT and histomorphometrical evaluation were performed at 8 and 16 weeks. MSC were obtained from healthy volunteers and patients with lymphoid malignancy. Human MSC survived in the defect for the entire duration of the trial. MSC from healthy volunteers, in contrast to hMSC from cancer patients, significantly improved bone healing at 8, but not 16 weeks. However, at 16 weeks, hMSC significantly improved vasculogenesis in residual defect. We conclude that hMSC from healthy donors significantly contributed to the healing of bone defects at 8 weeks and to the vascularisation of residual connective tissue for up to 16 weeks. We found the administration of hMSC to be safe, as no adverse reaction to human cells at the site of implantation and no evidence of migration of hMSC to distant organs was detected.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a femur $x diagnostické zobrazování $x fyziologie $7 D005269
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a syndromy imunologické nedostatečnosti $x diagnostické zobrazování $x imunologie $x terapie $7 D007153
- 650 _2
- $a mužské pohlaví $7 D008297
- 650 _2
- $a transplantace mezenchymálních kmenových buněk $x metody $7 D045164
- 650 _2
- $a mezenchymální kmenové buňky $x fyziologie $7 D059630
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a osteogeneze $x fyziologie $7 D010012
- 650 _2
- $a náhodné rozdělení $7 D011897
- 650 _2
- $a krysa rodu Rattus $7 D051381
- 650 _2
- $a potkani nazí $7 D011923
- 650 _2
- $a počítačová rentgenová tomografie $x metody $7 D014057
- 650 _2
- $a výsledek terapie $7 D016896
- 650 _2
- $a hojení ran $x fyziologie $7 D014945
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a Rentsch, Claudia, $d 1983- $7 xx0209603 $u Translational Bone, Joint and Soft Tissue Research, Medical Faculty and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany
- 700 1_
- $a Soukup, Tomáš, $d 1980- $7 xx0036274 $u Institute of Histology and Embryology, Medical Faculty Hradec Králové, Charles University, Hradec Králové, Czech Republic
- 700 1_
- $a Novotný, Ladislav, $d 1950- $7 xx0105828 $u Radioisotope Laboratory and Animal House, Medical Faculty Hradec Králové, Charles University, Hradec Králové, Czech Republic; Finn Pathologists, One Eyed Lane, Weybread, Norfolk, IP21 5TT, United Kingdom
- 700 1_
- $a Rentsch, B. $u Translational Bone, Joint and Soft Tissue Research, Medical Faculty and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany
- 700 1_
- $a Kanderová, Veronika $7 xx0200317 $u CLIP - Childhood Leukaemia Investigation Prague, Department of Paediatric Haematology and Oncology, Second Medical Faculty, Charles University, Prague and Motol University Hospital, Prague, Prague, Czech Republic
- 700 1_
- $a Rychtrmocová, Hana $7 xx0209604 $u First Department of Medicine, First Medical Faculty, Charles University, Prague and General University Hospital, Prague, Czech Republic
- 700 1_
- $a Kalmárová, Markéta $7 xx0095356 $u First Department of Medicine, First Medical Faculty, Charles University, Prague and General University Hospital, Prague, Czech Republic
- 700 1_
- $a Stehlík, David $7 xx0138007 $u Institute of Anatomy, First Medical Faculty, Charles University, Prague, Czech Republic; Department of Orthopedics, Second Medical Faculty, Charles University, and Motol University Hospital, Prague, Czech Republic
- 700 1_
- $a Trněný, Marek, $d 1960- $7 nlk20000083659 $u First Department of Medicine, First Medical Faculty, Charles University, Prague and General University Hospital, Prague, Czech Republic
- 700 1_
- $a Slanař, Ondřej $7 xx0058262 $u Institute of Pharmacology, First Medical Faculty, Charles University, Prague and General University Hospital, Prague, Czech Republic
- 773 0_
- $w MED00003824 $t Physiological research $x 1802-9973 $g Roč. 66, č. 1 (2017), s. 113-123
- 856 41
- $u http://www.biomed.cas.cz/physiolres/ $y stránka časopisu
- 910 __
- $a ABA008 $b A 4120 $c 266 $y 4 $z 0
- 990 __
- $a 20170824 $b ABA008
- 991 __
- $a 20190514105937 $b ABA008
- 999 __
- $a ok $b bmc $g 1246217 $s 986967
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2017 $b 66 $c 1 $d 113-123 $e 20161026 $i 1802-9973 $m Physiological research $n Physiol. Res. (Print) $x MED00003824
- GRA __
- $a NT13531 $p MZ0
- LZP __
- $b NLK118 $a Pubmed-20170824