Name
|
Authors
|
Characteristics
|
Diffenrentiation capacity
|
ES cells
|
Numerous
|
Capable of mass culture.
Immunosuppressive agents
required for allogeneic
transplantation.
|
Can differentiate into wide variety
cells, but cells capable of
differentiating in the early embryonic
period are to obtain in vitro.
|
Bone marrow
mesenchymal
stem cells
|
Fukuda et al,
Keio Univ.
|
Culture method relatively
easy.
|
Osteoblasts, chondroblasts,
adipocytes, cardiomyocytes, etc.
|
MAPC cells
|
Verfeille et al,
University
of Minnesota
|
Culture¡¡method extremely¡¡difficult.
Mass culture impossible.
|
Can differentiate into wide variety cells
including neurons, hepatocytes,
skeletal muscle cells.
|
Myocardial tissue
stem cells
(c-Kit cells)
|
Anversa et al,
State University
of New York
|
Isolation difficult.
Mass culture impossible.
|
Myocardium, smooth muscle, vascular
endothelial cells.
|
Myocardial tissue
stem cells
(Sca-1 cells)
|
Schneider et al,
Baylor University
|
Isolation difficult.
Mass culture impossible.
|
Myocardium
|
Cd133 cells
|
Rafii S, Lyden D.
Rehman J, Li J, Orschell CM, March KL.
|
neovascularization and differentiate into mature
endothelial cells.
|
Endothelial cell
|
EPC
|
Asahara T, Kawamoto A.
|
neovascularization and differentiate into mature
endothelial cells
releasing paracrine factors.
|
Endothelial cell
|
Study
|
[n] and
Cell Type
|
Delivery
|
Time After
AMI
|
Outcomes
|
||
Improved
|
No Change
|
|||||
Strauer et al
|
10 treated, 10 controls* MNC
|
IC
|
5?9 days
|
Regional wall motion?;
|
Global LVEF;
|
|
Infarct size¡ý Perfusion?
|
LVEDV?
|
|||||
TOPCARE-AMI
|
29 MNC, 30 CPC, MNC
11 controls* CPC
|
IC
|
5_2 days
|
Regional wall motion?;
|
LVEDV?
|
|
Global LVEF?;
|
||||||
Infarct size 2?;
|
||||||
Coronary flow?
|
||||||
Fernandez-Aviles et al
|
20 treated, 13 controls* MNC
|
IC
|
14_6 days
|
Regional wall motion?;
|
LVEDV?
|
|
Global LVEF?
|
||||||
Kuethe et al
|
5 treated MNC
|
IC
|
6 days
|
Regional wall motion?;
|
||
Global LVEF?
|
||||||
BOOST
|
30 treated, 30 controls NC
|
IC
|
6_1 day
|
Regional wall motion;
|
LVEDV; Infarct size
|
|
Global LVEF
|
||||||
Chen et al
|
34 treated, 35 controls MSC
|
IC
|
18 days
|
Regional wall motion;
|
||
Global LVEF;
|
||||||
Infarct size ¡ý;
|
||||||
LVEDV ¡ý
|
||||||
Vanderheyden et al
|
12 treated, 10 controls* CD133?
|
IC
|
14_6 days
|
Regional wall motion?;
|
||
Global LVEF?; Perfusion?
|
||||||
Study
|
[n]
|
LVEF
|
Cell Type
|
Time after
|
Delivery
|
Outcomes?
|
MI
|
||||||
Menasche et al
|
10 treated
|
24_4£¥
|
Myoblasts
|
3?228
months
|
Transepicardial
(during CABG)*
|
Regional wall motion ¡ü;
Global LVEF¡ü
|
Herreros et al
|
11 treated
|
36_8£¥
|
Myoblasts
|
3?168
months
|
Transepicardial
(during CABG)?
|
Regional wall motion ¡ü;
Global LVEF ¡ü; Viability in infarct area ¡ü
|
Siminiak et al
|
10 treated
|
25?40£¥
|
Myoblasts
|
4?108
months
|
Transepicardial
(during CABG)?
|
Regional wall motion ¡ü;
Global LVEF ¡ü
|
Chachques et al
|
20 treated
|
28_3£¥
|
Myoblasts
|
not
reported
|
Transepicardial
(during CABG)*
|
Regional wall motion ¡ü;
Global LVEF ¡ü; Viability in
infarct area ¡ü
|
Smits et al
|
5 treated
|
36_11£¥
|
Myoblasts
|
24?132
months
|
Transendocardial
(guided by EMM)
|
Regional wall motion ¡ü;
Global LVEF ¡ü
|
Stamm et al
|
12 treated
|
36_11£¥
|
CD133?
|
3?12
weeks
|
Transepicardial
(during CABG)*
|
Global LVEF ¡ü; LVEDV ¡ý;
Perfusion ¡ü
|
Assmus et al
|
51 MNC, 35 CPC, 16 controls
|
40_11£¥
|
MNC CPC
|
3?144 months
|
IC
|
Global LVEF ¡ü; (only in MNC group)
|
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