Stem cells therapy for peripheral arterial occlusive disease

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Stem Cells Therapy for Peripheral Arterial Occlusive Disease Dong-Ik Kim, MD. , Ph.D ([email protected]) Division of Vascular Surgery, Samsung Medical Center Sungkyunkwan University School of Medicine, Seoul, Korea

Transcript of Stem cells therapy for peripheral arterial occlusive disease

Stem Cells Therapy for Peripheral Arterial Occlusive Disease

Dong-Ik Kim, MD. , Ph.D ([email protected])Division of Vascular Surgery, Samsung Medical Center

Sungkyunkwan University School of Medicine, Seoul, Korea

Prospect of Stem Cell Therapy

• Will the stem cell be effective for the

treatment of peripheral arterial occlusive

disease in the future?

Yes, it will be.

Evidences of Stem Cell Effect

• Animal Study

• Clinical Study

Animal Study (2002 - )

• Whole bone marrow stem cell

• Bone marrow derived mononuclear cell

• Bone marrow derived MSC

• Cord blood derived MNC

• Cord blood derived MSC

• Adipose tissue derived MSC

vWF HNA Merge

Angiogenesis : Differentiated from injected stem cell

Angiogenesis - angiogram

Control Treat

Dog Ischemic Limb Model- Mongrel Dog : male, 20-25 ㎏ - Femoral Arteries : occluded with ameroid constrictor

Mouse limb ischemia model

Animal Model

• Methods of stem cell injection : intramuscular injection

• Harvest : 8 weeks & 6 month after stem cell injection

• Assessment for angiogenic effect

1) Angiography

2) Immunohistochemical staining

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1.2

1.4

1.6

1.8

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2.2

2.4

capillary rato

HCB-MNC

Control 4x10^6 4x10^7 4x10^8

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Human cord blood mononuclear cell transplantation : capillary ratios

Human cord blood mononuclear cell transplantation: Angiogenic factor - Western blot

(A) (B) (C)

(D) (E) (F)

Human cord blood mononuclear cell transplantation : Angiogenic factor - Tunnel assay & immunohistochemical stain

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* **

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Human cord blood mononuclear cell transplantation : Angiogenic gene expression - Real Time-PCR

Conclusions from animal study

• Angiogenesis comes from injected stem cells

• Paracrine effect of injected stem cells

1) secretion of cytokines : PDGF, VEGF etc.

Evidences of Stem Cell Effect

• Animal Study

• Clinical Study

Lists of Clinical Trials

• Autologous whole bone marrow stem cell implantation : Tibia bone fenestration technique (2004- 2006 )

• Autologous whole bone marrow stem cell implantation :

aspiration from iliac bone (2007- 2009)

• Homologous HCB-MNC Injection (2008-2010)

• Homologous HCB-MSC transplantation (2011- 2012)

T F

Autologous whole bone marrow stem cell implantation (2004):

Tibia bone fenestration technique

Demographics

• Total 27 patients ( 34 limbs)

• 26 male (33 limbs) / 1 female (1 limb)

• Mean age : 37.6 ± 6.9 years

• Mean FU periods : 19.1 ± 3.5 month (12.4 - 25month)

Angiographic findings

* (A, C, E) : pre-operative status (B, D, F) : post-operative status

* B : +1 D : +2 F : +3 angiogenic status

Results : Angiogram

Classification Limbs

+3 2

+2 5

+1 9

0 6

* postoperative angiogram were obtained in 22

limbs among 34 limbs.

Pre stem cell therapy

Poststem cell therapy

Rates of clinical improvement : 79.7 %

Clinical Trials

• Autologous whole bone marrow stem cell implantation : Tibia bone fenestration technique (2004- 2006 )

• Autologous whole bone marrow stem cell implantation :

aspiration from iliac bone (2007- 2009)

• Homologous HCB-MNC Injection (2008-2010)

• Homologous HCB-MSC transplantation (2011- 2012)

VİDEO

July 2004 - June 2009

90 ischemic limbs with 67 patients 1. Mean age: 39.8 ± 7.9 years 2. Mean follow-up period: 29.3 ± 18.1 months

Symptoms 1. Intermittent claudication : 44 limbs 2. Critical limb ischemia : 46 limbs

Demographics

Angiographic outcomes (n=37)1. recanalization of the run-off vessels: 3 limbs (8.1%)2. development of new collateral vessels (angiogenesis) : 16 limbs (43.2%)3. increased diameter and/or length of preexisting collateral vessels (arteriogenesis) : 15 limbs (40.5%)

Rates of angiographic improvement : 43.2 %

Rates of clinical improvement : 55.6 %

Results

Number of injected cells

Total MNCs (/ml) CD34+ (/ml)

Mean No. P Mean No. P

PB

Day 0 2.71×106 ± 1.13×106 0.247 2.23×105 ± 2.57×105 0.620

Day 1 3.19×106 ± 1.77×106 0.688 3.34×105 ± 3.43×105 0.509

Day 2 2.87×106 ± 1.68×106 0.472 3.59×105 ± 4.61×105 0.906

BM Day 3 4.46×106 ± 1.02×107 0.090 1.62×105 ± 2.53×105 0.167

CD133+ (/ml) CD34+CD133+ (/ml)

Mean No. P Mean No. P

PB

Day 0 1.22×105 ± 1.61×105 0.943 6.19×104 ± 1.63×105 0.143

Day 1 2.13×105 ± 2.42×105 0.464 8.38×104 ± 9.19×104 0.150

Day 2 2.04×105 ± 2.05×105 0.706 6.84×104 ± 6.93×104 0.345

BM Day 3 1.16×105 ± 1.35×105 0.142 4.73×104 ± 6.74×104 0.225

Clinical Trials

• Autologous whole bone marrow stem cell implantation : Tibia bone fenestration technique (2004- 2006 )

• Autologous whole bone marrow stem cell implantation :

aspiration from iliac bone (2007- 2009)

• Homologous HCB-MNC Injection (2008-2010)

• Homologous HCB-MSC transplantation (2011- 2012)

• 7 ischemic limbs with 7 patients• Number of injected stem cells : 4×108

• Safety : No adverse effect • Rates of clinical improvement : 57%• Rates of angiographic improvement : 71.4%

Homologous HCB-MNC Injection

Clinical Trials

• Autologous whole bone marrow stem cell implantation : Tibia bone fenestration technique (2004- 2006 )

• Autologous whole bone marrow stem cell implantation :

aspiration from iliac bone (2007- 2009)

• Homologous HCB-MNC Injection (2008-2010)

• Homologous HCB-MSC transplantation (2011- 2012)

• Title : The Safety of Human Cord Blood-derived Mesenchymal Stem Cells Therapy in Patients with PAOD : Phase I Clinical Study• KFDA approval : 2011. 5 • IRB approval from SMC : 2011. 5 • Target disease : peripheral arterial occlusive disease• Inclusion criteria : Rutherford’s classification IIb, III, IV• Source of Stem Cells : Human Cord Blood-derived Mesenchymal Stem Cells • Injected cell number : 1 X 107 • Injection site : calf muscle & vicinity of tibioperoneal artery

HCB –MSC injection (Phase I Study)

• Primary endpoint : Safety evaluation (1,3,6 month)1) death 2) cardiovascular event3) anaphylactic shock or allergic reaction4) acute or chronic graft-versus host disease5) procedure-related complications

• Secondary endpoint1) wound healing rate2) change of segmental limb pressure3) change of the scale for gauging changes in clinical status

End Point of Phase I study

NoAGE

pre postGauging change

Angio TotalRutherford category

Sx VAS ABIRutherford category

Sx VAS ABI

1 31 5 Ulcer 7 ATA 0.31PTA 0.46

2 Healed 0 ATA 0.44PTA 0.47 +1 +2

2 46 3 Claudication 7 ATA 0

PTA 0.682 improve 1 ATA 0

PTA 0.8 +2

3∫ 72 3 Claudication 7 ATA 0.24

PTA 0.472 improve 3 ATA 0.46

PTA 0.52 +1 +2

4 56 4 Claudication 7

ATA 0.26PTA 0.3

3 improve 5ATA 0.19 PTA 0.73 +2

5 56 5 Ulcer 8 ATA 0.32PTA 0.36

4 Healed 2 ATA 0.19PTA 0.33 +1

6* 48 5 Ulcer 10 ATA 0PTA 1.02

1 Healed 1 ATA 1.18PTA 0.94 +2

7 77 6 Ulcer 6ATA 0.57PTA

06 improve 2

ATA 0.56PTA

00 +1

8 48 3 Claudication 8 ATA 0.4

PTA 0.613 improve 5 ATA 0.25

PTA 0.44 0

9∬ 44 5 Ulcer 5 ATA 0.55PTA 0.68

5 improve 2 ATA 0.59PTA 0.68 0

10* 47 5 Ulcer 5 ATA 1.08PTA 0.68

1 Healed 0 ATA 1.09PTA 0.74 +1

*: Toe amputation, ∫: Cr elevation, ∬: urticaria

Results : HCB –MSC injection

• Ministry of Health and Welfare• Approve the autologous bone marrow stem cell therapy for PAOD

as a New Health Technology (2013.2)• Autologous Bone Marrow Stem Cell Transplantation became a

common treatment modality to the patient for PAOD in Korea.

Stem Cell therapy for PAOD in Korea

Conclusions from clinical trials

• Stem cell therapy is safe and effective for the treatment for the peripheral arterial occlusive disease.

What’s your choice?

International Journal of Stem Cells (http://www.ijstemcell.com)

Acknowledgment

Thank you