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NIPERD HARISH PADH [email protected] VICE CHANCELLOR SARDAR PATEL UNIVERSITY Stem Cells: Potential for Therapy

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Page 1: NIPERD Stem Cells: Potential for Therapy. Replacement parts needed for transplantation or tissue reconstruction Replacement parts needed for transplantation

NIPERD

HARISH [email protected]

VICE CHANCELLORSARDAR PATEL UNIVERSITY

Stem Cells: Potential for Therapy

Page 2: NIPERD Stem Cells: Potential for Therapy. Replacement parts needed for transplantation or tissue reconstruction Replacement parts needed for transplantation

Replacement parts needed for

transplantation or tissue reconstruction

Tissue Engineering

PROBLEM

Page 3: NIPERD Stem Cells: Potential for Therapy. Replacement parts needed for transplantation or tissue reconstruction Replacement parts needed for transplantation

Replacement parts needed for

transplantation or tissue reconstruction

Tissue Engineering

Solution: STEM CELLS

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Stem Cells

Stem cells are potentially immortal cells capable of self-renewal and also give rise to differentiated cells

No area of research since gene therapy has evoked so much enthusiasm and hope

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Stem cells are body ‘master cells’ Differ from mature cells which are fully committedStem cells are thus reserve supply of replacement cells that multiply when needed Formed at conception & gradually become specialized Our body retains stem cell reserves in various organs to replace diseased tissue As the stem cell reserve gets depleted, we succumb to diseases, disorders and process of aging

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Embryonic Stem Cells

Longer life span, almost ‘immortal’

High degree of plasticity – Pluripotent

Easier to isolate and cultivate

Limitless supply of cells in culture

More genetic stability

Ethical issues

Form teratomas

Will face immune rejection

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Embryonic Stem Cells

Thomson et al Science, 1998

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Fischbachand FischbachJ. Clin. Inv. 114:1364

Self-renewal: can divide indefinitely

Can undergo asymmetric division

Retain the capacity to develop into any adult cell type

Properties of Pluripotent Stem Cells

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Oct-4 (Pou-Transcription factor)

Stage Specific Embryonic Antigens

SSEA-3SSEA-4

Tumor Recognition Antigens

TRA-1-60TRA-1-81

High Alkaline Phosphatase activity

High Telomerase Activity

Characterization of hES Cells

Karyotyping

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Therapeutic Potential

Diabetes 1

Neurodegenerative disorders Myocardial infarction

Spinal cord injury

Severe liver damage

Haematological disorders

Severe eye and ear damage

Cell transplantation therapy

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Homoeostasis

Balance of Cell Supply

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EVERYDAY NEED

5 m x 1000 x 40 = 200 billion per day RBC

5000 x 1000 x 40 = 200 million per day WBC

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Figure: Measurement of ROS in SKO- and SKOM- infected MEF compared to empty vector. D indicates day hereafter

Stem Cells

Embryonic Stem Cells Adult Stem Cells

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Adult Stem Cells

Maintain capacity for self-renewal

Undergo asymmetric division or development

Differentiate to limited subset of cell types

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Hematopoietic Fetal liver & spleen, bone marrow, peripheral blood, umbilical cord blood

Liver Portal zone near bile duct

Intestine Crypts

Epidermal Basal layer of skin

Limbal stem cells Pigmented ciliary margin

Breast Epithelium Cap cells and basal layer of mammary gland

Pancreas Islets and ducts

Mesenchymal Bone marrow stroma, adipose tissue

Tooth & Ear

Placenta

Germline stem cells Testis, Ovary (?)

Adult Stem Cells - Sources

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DISEASES THAT CAN BE TREATED WITH CORD BLOOD STEM CELLS

CancersAcute and Chronic Leukemia High-Risk Solid Tumors Hodgkin & Non-Hodgkin Lymphoma Myelodysplastic Syndrome

Blood DisordersBeta Thalassemia Diamond-Blackfan Anemia , Fanconi Anemia, Severe Aplastic Anemia Sickle Cell Disease

Immune DisordersChronic Granulomatous Disease Hystiocytic Disorders Leukocyte Adhesion Deficiency Severe Combined Immunodeficiency Diseases Wiskott-Aldrich Syndrome

Metabolic DisordersKrabbe Disease Hurler Syndrome Metachromatic Leukodystrophy Sanfilippo Syndrome

Cord Blood Registry, www.cordblood.com

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Adult Stem Cells Embryonic Stem Cells IPS

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Induced pluripotent stem cells ?

iPS cells are a type of pluripotent stem cell from an adult somatic cell, by inducing a "forced" expression of certain genes.

iPS cells believed to be identical to natural pluripotent stem cells, such as embryonic stem cell in many respects, such as

• the expression of certain stem cell genes and proteins, • chromatin methylation patterns, • embryoid body formation, • teratomas formation,• viable chimera formation, • potency and, • differentiability.

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A Brief History of iPS Findings

2006

2007

2007

2008

2007

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SOX2This intron less gene encodes a member of the SRY-related HMG-box (SOX) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate.

MYCThe protein encoded by this gene is a multifunctional, nuclear phosphoprotein that plays a role in cell cycle progression, apoptosis and cellular transformation. It functions as a transcription factor that regulates transcription of specific target genes. Mutations, overexpression, rearrangement and translocation of this gene have been associated with a variety of hematopoietic tumors

KLF4 Kruppel-like factor 4 Klf4 functions upstream of Nanog in ES cell self-renewal and in preventing ES cell differentiation. Klf4 interacts directly with Oct4 and Sox2 when expressed at levels sufficient to induce induced pluripotent stem cells

OCT4 (POU class 5 homeobox 1)This gene encodes a transcription factor containing a POU homeodomain. This transcription factor plays a role in embryonic development, especially during early embryogenesis, and it is necessary for embryonic stem cell pluripotency

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• New tools for studying development• Development of disease models• Novel cell-based therapies

Patient specific iPS lines could overcome problem of immune rejection• Avoid most ethical considerations

associated with hES cells iPS

Fischbachand Fischbach, J. Clin. Inv. 114:1364

Why are iPS Cells Useful?

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FIRST STEM CELL CLINICAL TRIAL APPROVED BY FDA

Food and Drug Administration (FDA) had approved the first-ever clinical trial of stem cell therapy on human subjects, in 2009.

The trial, funded by the biotech company Geron, was to test a procedure to repair spinal cord damage.

The therapy involves the injection of precursor cells into the spine, where the cells will then differentiate into oligodendrocytes, the cells type that sheathes and protects the nerves of the spinal cord.

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CLINICAL TRIALS IN WORLD FOR FOLLOWING DISORDERS

Non-Ischemic Congestive Heart Failure

Chronic Obstructive Pulmonary DiseaseStem Cells Trial in Acute Ischemic StrokeCord Blood Infusion in Children with Cerebral PalsyPeripheral arterial disease (leg blood vessel disease)

Severe Intermittent Claudication

Poor Blood Flow to the Heart

Type 1 Diabetes

Type 2 DiabetesFistulas Due to Crohn's Disease

Secondary Progressive Multiple Sclerosis

Frailty SyndromeAdult Stem Cell Research Network, www.ascrnetwork.com

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Trounston et al. BMC Medicine 2011, 9: 52

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Trounston et al. BMC Medicine 2011, 9: 52

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Trounston et al. BMC Medicine 2011, 9: 52

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Trounston et al. BMC Medicine 2011, 9: 52

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Study Condition Intervention Status

Safety and efficacy of autologous bone marrow stem cells in patients with spinal cord injury

Spinal cord injury

Autologous bone marrow derived stem cells

Recruiting

Mesenchymal stem cells in critical limb ischemia

Critical limb ischemia

Mesenchymal stem cells; Plasmalyte A

Active, not recruiting

Clinical trial to study the efficacy and safety of different doses of bone marrow derived mesenchymal stem cells in patients with critical limb ischemia due to Buergers disease

Critical limb ischemia; Buerger’s disease

Allogenic mesenchymal stem cells; Standard protocol of care

Not yet recruiting

Ex vivo cultured bone marrow derived allogenic MSCs in AMI

Myocardial infarction

Stem cells; Plasmalyte A

Active, not recruiting

Allogenic mesenchymal stem cells in osteoarthritis

Osteoarthritis of knee

Ex-vivo cultured adult allogenic MSCs; Plasmalyte A

Recruiting

www.clinicaltrials.gov

Stem cell clinical trials in India- Present status

Page 33: NIPERD Stem Cells: Potential for Therapy. Replacement parts needed for transplantation or tissue reconstruction Replacement parts needed for transplantation

Study Condition Intervention Status

Safety and efficacy of autologous bone marrow stem cells for treating osteoarthritis

Osteoarthritis Autologous bone marrow stem cells

Enrolling by invitation

Autologous mesenchymal stem cell transplant for Parkinson’s disease

Parkinson’s disease

Autologous bone marrow derived stem cells

Active, not recruiting

Safety and efficacy of autologous bone marrow stem cells for treating chronic renal failure

Chronic renal failure

Autologpus bone marrow stem cells

Recruiting

Efficacy of autologous bone marrow derived stem cell transplantation in patients with type 2 Diabetes Mellitus

Type 2 Diabetes Mellitus

Stem cell harvest; Angiographic transplantation of stem cells

Unknown

Evaluation of the role of mesenchymal stem cells in the treatment of graft versus host disease

Graft vs Host disease

Mesenchymal stem cell infusion

Unknown

www.clinicaltrials.gov

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Study Condition Intervention Status

Efficacy of autologous bone marrow derived stem cell transplantation in patients with Type 2 Diabetes Mellitus-2

Type 2 Diabetes Mellitus

Stem cell transplantation

Unknown

Clinical trial on diabetic foot using peripheral blood derived stem cells for treating critical limb ischemia

Diabetic foot; critical limb ischemia; leg ulcers

Will receive G-CSF and peripheral blood derived mononuclear cells; G-CSF; Standard therapy

Unknown

Safety and efficacy of autologous bone marrow stem cells in treating spinal cord injury

Spinal cord injuries

Laminectomy; Intrathecal

Completed

Pilot study of efficacy of Lactobacillus CD2 Lozenges in preventing high-dose chemotherapy induced oral mucositis in patients undergoing hematopoietic stem cell transplantation

Oral mucositis

Lactobacillus CD2 lozenges

Recruiting

www.clinicaltrials.gov

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Study Condition Intervention Status

Study of the monoclonal antibody CT-011 in diffuse large B-Cell lymphoma following autologous stem cell transplantation

Lymphoma, Large cell, diffuse; Lymphoma, Mixed cell, diffuse; Primary Mediastinal Large B-cell lymphoma; Transformed follicular lymphoma; Relapsed

CT-011 Completed

BMAC enhanced coronary artery bypass grafting (CABG)

Congestive heart failure

Harvest SmartPReP2 BMAC system

Recruiting

www.clinicaltrials.gov

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Study Condition Intervention Status

Safety and efficacy of autologous bone marrow mononuclear cells in patients with severe critical limb ischemia

Critical limb ischemia

Autologous bone marrow mononuclear cells

Recruiting

Granulocyte colony stimulating factor (G-CSF) in acute liver failure and alcoholic hepatitis

Liver failure, acute

Grnaulocyte colony stimulating factor

Recruiting

G-CSF and erythropoetin in survival of patients with decompensated liver disease

Chronic liver disease

G-CSF+EPO; Placebo

Recruiting

Efficacy of granulocyte colony-stimulating factor and erythropoetin for patients with acute-on-chronic liver failure

Acute on chronic hepatic failure

Granulocyte colony stimulating factor (G-CSF) and Erythropoeitin (EPO); Placebo

Recruiting

www.clinicaltrials.gov

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Study Condition Intervention Status

Feasibility study of autologous bone marrow aspirate concentrate for treatment of CLI

Arterial occlusive diseases

SmartPReP2 BMAC system

Active, not recruiting

Safety and efficacy evaluation of two year imatinib treatment in adjuvant gastrointestinal stromal tumor (GIST)

Gastrointestinal stromal tumors

Imatinib mesylate

Active, not recruiting

Study of NTx-265: Human Chorionic Gonadotropin (hCG) and Epoetin Alfa (EPO) in acute ischemic stroke patients

Stroke Human chorionic gonadotropin (hCG), epoetin alfa (EPO); Saline Placebo

Terminated, Has results

REGENESIS (CA): A study of NTxTM-265: Human Chorionic Gonadotropin (hCG) and Epoetin Alfa (EPO) in acute ischemic stroke patients

Stroke NTxTM-265; rhCG, rEPO; Saline placebo

Terminated

www.clinicaltrials.gov

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Study Condition Intervention Status

Chemotherapy in treating patients with acute lymphoblastic leukemia and diffuse non-hodgkin’ s lymphoma

Leukemia; Lymphoma

Asparaginase; cyclophosphamide; cytarabine; daunorubicin hydrochloride; doxorubicin hydrochloride; etoposide; ifosfamide; mercaptopurine; methotrexate; prednisone; vincristine sulfate; conventional surgery; radiation therapy

Unknown

www.clinicaltrials.gov

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Sardar Patel UniversityVallabh Vidyanagar

Thank [email protected]