Editorial
Copyright ©2011 Baishideng Publishing Group Co.
World J Stem Cells. Apr 26, 2011; 3(4): 25-33
Published online Apr 26, 2011. doi: 10.4252/wjsc.v3.i4.25
Table 1 Differentiated phenotype given rise from adipose-derived stromal cell and interactive effects of these cells with immune and cancer cells
Phenotype given rise in in vitro systemRef.
Classic mesenchymal phenotype (adipocyte, osteoblast, chondrocyte)[1]
Hematopoietic supporting cells[25]
Other phenotypesVascular cells (Smooth-muscle cells, Endothelial)[16]
Neurones[1]
Cardiomyocyte and skeletal cells in the required presence of 5 azacytidine[16]
Modulation of inflammation and immune suppressive functionsRheumatoid arthritis[31]
GVH[30]
Autoimmune encephalomyelitis[32]
Anti-cancer effectTumor progression inhibition[34]
Pro-cancer effectsTumor progression growth[35,37]
Table 2 The different steps for a clinical trialand cancer cells
Steps of clinical trialElements of discussion
DesignAutologous
Immunocompatibility
Lag of time between fat sampling and delivery
Amount of cells
Allogenic
Histocompability issue
If bank, ready to use treatment
Inclusion criteria
Too broad: leads to wrong conclusions associated with great variability and independent parameters,
Too restricted: enrolment difficulties associated with non relevant and inadequate parameters
Exclusion criteria
Too broad: enrolment difficulties associated with non relevant and inadequate parameters
Too restricted: risks of adverse side effects associated with interactions between transplanted cells and undesirable context
Number of patients: statistically defined
Objective and well-established criteria of safety and efficacy
Uni or multicenter analysis
Standardization of procedures between centers
Efficiency of enrolment
SamplingLiposuction:
Local anesthesia
Fat depot
Technique (no ultra-sound)
Anti-coagulant
CultureOpened or closed system
Bovine or human-derived products
Number of passages
Quality and Safety control
Release criteria
Injectioniv
Poorly invasive but large distribution and mostly trapped in lung
im or intra tissue
More invasive
More restricted localization
Pressure challenge for adipose-derived stromal cells
Monitoring of the tolerance and the safetyCriteria: pain, wound healing, inflammation, immunology, tumor
Kinetics for analysis
Short and long term safety
Monitoring of the resultsObjective criteria, standardisation of procedures
Analysis of the resultsAdequate statisitic
Stick to primary and secondary aims
Table 3 Clincial trials using stromal vascular fraction
Clinical trials with SVFDesignResultsRef
Traumatic calvaria defectAutologous SVF + fibrin glue: case reportSuccess{Lendeckel, 2004 #483}
Breast reconstruction after lumpectomyAutologous fat + autologous SVF. No arm controlCysts and Microcalcifications (4/70 patients){Yoshimura, 2008 #481} {Yoshimura, 2008 #481}
Autologous fat + autologous SVF, phase IVNCT00616135*
Lipodystrophy IAutologous SVF + fatrecruitingNCT00715546*
Phase I
Non revascularizable myocardiumAutologous SVFongoingNCT00426868*
Injection into the left ventricle
Treatment of Pts With ST-Elevation Myocardial InfarctionAutologous SVF, Phase IOngoingNCT00442806*
Injection into the left ventricle
Autologous SVF, 2 doses against placebo, Phase II, III, Intracoronary injectionNot yet openNCT01216995*
Diabetes I“Activated” autologous SVF, phase I/IIrecruitingNCT00703599*
iv administration
Diabetes II“Activated” autologous SVF, phase I/IIrecruitingNCT00703612*
Liver cirrhosisAutologous SVFSuspendedNCT00913289*
Intrahepatic arterial administrationsuspendedNCT01062750
Table 4 Clincial trials using adipose-derived stromal cell
Clinical trials with ADSCDesignResultsRef
Maxillary reconstructionAutologous ADSC case reportSuccess{Mesimaki, 2009 #480}
Cryptoglandular origin fistula with or without Crohn’s diseaseAutologous ADSC phase I/II intra-tissueADSCs more effective (P = 0.001). Recurrence rate with ADSC = 17.6%{Garcia-Olmo, 2008 #451; Garcia-Olmo, 2009 #449}
Autologous ADSCOngoing, not recruitingNCT00115466*
Phase II, 2 arms (fibrin glue, fibrin glue + ADSC)
Crohn’s disease fistulaAutologous ADSC, phase I and IIPhase I, completeNCT00992485*
Phase II recruitingNCT01011244*
Autologous ADSC, phase IPhase I/II recruitingNCT01157650*
Allogenic ADSC: phase I/IIrecruitingNCT00999115*
20 × 106 then 40 × 106
Complex Perianal Fistulas not associated to Crohn’s diseaseAutologous ADSC, phase III three arms (fibrine, ADSC, fibrin glue + ADSC; 20 × 106 then 40 × 106 when no effect)Completed (214 enrolled patients)NCT00475410*
Long term safetyRecruitingNCT01020825*
Depressed ScarAutologous ADSC predifferentiated towards adipocyte, phase II, IIICompleteNCT00992147*
Chronic critical limb IschemiaAutologous ADSC, phase IRecruitingNCT01211028*
im 100 × 106
Chronic critical limb Ischemia in diabetic patientsAutologous ADSC, phase I/IIRecruitingNCT01079403*
iv administration
Fecal incontinenceAutologous ADSC, phase IRecruitingNCT01011686*
GVHDAutologous ADSC4/5 alive (after a median follow-up of 40 mo){Fang, 2007 #469}
iv 106/kg
Autologous ADSCRecruitingNCT01222039
Three arms no administration, iv 106/kg or 3 × 106/kg
Secondary Progressive Multiple SclerosisAutologous ADSC phase I/IIRecruitingNCT01056471*
3 arms (iv 106 and 4 × 106/kg against no intervention)