Treatment of stroke and other acute neural degenerative disorders using postpartum-derived cells

• US 8,361,459 B2
• Filed: 01/29/2010
• Issued: 01/29/2013
• Est. Priority Date: 06/27/2003
• Status: Active Grant

• Current Assignee: DePuy Synthes Products LLC (Johnson & Johnson)
• Original Assignee: Advanced Technologies and Regenerative Medicine, LLC
• Inventors: Messina, Darin J., Mistry, Sanjay K., Hong, L. S. Klaudyne, Kramer, Brian C., Romanko, Michael J., Gosiewska, Anna
• Primary Examiner(s): Gamett, Daniel C
• Application Number:
  US12/697,081
• Publication Number:
  US 20100215714A1
• Time in Patent Office: 1,096 Days
• Field of Search: None
• US Class Current: 424/93.7
• CPC Class Codes: A61K 2300/00 Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
• CPC Class Codes: A61K 35/12 Materials from mammals; Compositions comprising non-specified tissues or cells; Compositions comprising non-embryonic stem cells; Genetically modified cells vaccines or medicinal preparations containing antigens or antibodies A61K39/00
• CPC Class Codes: A61K 35/30 Nerves; Brain; Eyes; Corneal cells; Cerebrospinal fluid; Neuronal stem cells; Neuronal precursor cells; Glial cells; Oligodendrocytes; Schwann cells; Astroglia; Astrocytes; Choroid plexus; Spinal cord tissue
• CPC Class Codes: A61K 35/48 Reproductive organs
• CPC Class Codes: A61P 9/00 Drugs for disorders of the cardiovascular system
• CPC Class Codes: A61P 9/10 for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
• CPC Class Codes: C12N 2500/32 Amino acids
• CPC Class Codes: C12N 2500/34 Sugars
• CPC Class Codes: C12N 2500/44 Thiols, e.g. mercaptoethanol
• CPC Class Codes: C12N 2500/90 Serum-free medium, which may still contain naturally-sourced components
• CPC Class Codes: C12N 2500/95 Protein-free medium and culture conditions
• CPC Class Codes: C12N 2501/12 Hepatocyte growth factor [HGF]
• CPC Class Codes: C12N 2501/21 Chemokines, e.g. MIP-1, MIP-2, RANTES, MCP, PF-4
• CPC Class Codes: C12N 2501/23 Interleukins [IL]
• CPC Class Codes: C12N 2502/02 embryonic cells
• CPC Class Codes: C12N 2506/02 from embryonic cells
• CPC Class Codes: C12N 2506/03 from non-embryonic pluripotent stem cells
• CPC Class Codes: C12N 2509/00 Methods for the dissociation of cells, e.g. specific use of enzymes
• CPC Class Codes: C12N 2533/50 Proteins
• CPC Class Codes: C12N 5/0605 Cells from extra-embryonic tissues, e.g. placenta, amnion, yolk sac, Wharton's jelly
• CPC Class Codes: C12N 5/0607 : Non-embryonic pluripotent stem cells, e.g. MASC induced pluripotent stem cells C12N5/0696

Abstract

Cells derived from postpartum tissue such as the umbilical cord and placenta, and methods for their use to regenerate, repair, and improve neural tissue, and to improve behavior and neurological function in stroke patients are disclosed.

Claims

1. A pharmaceutical composition for treating a patient having an acute neurodegenerative condition, comprising a pharmaceutically acceptable carrier and umbilical cord tissue-derived cells in an amount effective to treat the neurodegenerative condition wherein the umbilical cord tissue-derived cells are derived from umbilical cord tissue substantially free of blood, wherein the cells are capable of self-renewal and expansion in culture and have the potential to differentiate into cells of at least a neural phenotype;

wherein the cells require L-valine for growth and can grow in at least about 5% oxygen;

wherein the cells do not produce CD117; and

wherein the cells further comprise at least one of the following characteristics;

a) potential for at least 40 doublings in culture;

b) production of at least one of tissue factor, vimentin, and alpha-smooth muscle actin;

c) production of at least one of CD10, CD13, CD44, CD73, CD90, PDGFr-alpha, PD-L2 and HLA-A,B,C;

d) lack of production of at least one of CD31, CD34, CD45, CD80, CD86, CD141, CD178, B7-H2, HLA-G, and HLA-DR,DP,DQ;

e) secretion of at least one of MCP-1, IL-6, IL-8, GCP-2, HGF, KGF, FGF, HB-EGF, BDNF, TPO, MIP1b, I309, MDC, RANTES, and TIMP1; and

f) lack of secretion of at least one of TGF-beta2, ANG2, PDGFbb, MIP1a, and VEGF, as detected by ELISA.

2. The pharmaceutical composition of claim 1, wherein the acute neurodegenerative condition results from ischemic or hemorrhagic stroke.

3. The pharmaceutical composition of claim 1, wherein the cells are induced in vitro to differentiate into a neural lineage cells prior to formulation of the composition.

4. The pharmaceutical composition of claim 1, wherein the cells are genetically engineered to produce a gene product that promotes treatment of the neurodegenerative condition.

5. The pharmaceutical composition of claim 1, comprising at least one other cell type.

6. The pharmaceutical composition of claim 5, wherein the other cell type is an astrocyte, oligodendrocyte, neuron, neural progenitor, neural stem cell, genetically engineered cell, or other multipotent or pluripotent stem cell.

7. The pharmaceutical composition of claim 1, comprising at least one other agent.

8. The pharmaceutical composition of claim 1, formulated for administration by injection or infusion.

9. The pharmaceutical composition of claim 1, wherein the cells are encapsulated within an implantable device.

10. The pharmaceutical composition of claim 1, wherein the cells are contained within a matrix or scaffold.

11. The pharmaceutical composition of claim 1 wherein the cells exert a trophic effect on the nervous system of a patient.

12. The pharmaceutical composition of claim 1 wherein the neurodegenerative condition is stroke.

13. A pharmaceutical composition for treating a patient having an acute neurodegenerative condition, which comprises a pharmaceutically acceptable carrier and a preparation made from the umbilical cord tissue-derived cells of claim 1, wherein the preparation comprises a cell lysate of the umbilical cord tissue-derived cells, an extracellular matrix of the umbilical cord tissue-derived cells or a conditioned medium in which the umbilical cord tissue-derived cells were grown.

14. The pharmaceutical composition of claim 1 wherein the cells are able to attach and expand on both coated and uncoated tissue culture vessels, wherein the coated tissue culture vessel comprises a coating of gelatin, laminin, collagen, polyornithine, vitronectin, or fibronectin.

15. The pharmaceutical composition of claim 1 wherein the cells exhibit increased expression, relative to a human cell that is a fibroblast, a mesenchymal stem cell, or an iliac crest bone marrow cell, of at least one gene encoding:

interleukin 8;

reticulon 1;

chemokine (C-X-C motif) ligand 1 (melonoma growth stimulating activity, alpha);

chemokine (C-X-C motif) ligand 6 (granulocyte chemotactic protein

     2);

chemokine (C-X-C motif) ligand 3; and

tumor necrosis factor, alpha-induced protein 3.

16. The pharmaceutical composition of claim 1 wherein the cells exhibit reduced expression, relative to a human cell that is a fibroblast, a mesenchymal stem cell, or an iliac crest bone marrow cell, of at least one gene encoding:

short stature homeobox 2;

heat shock 27 kDa protein 2;

chemokine (C-X-C motif) ligand 12 (stromal cell-derived factor

     1);

elastin cDNA DKFZp586M2022 (from clone DKFZp586M2022);

mesenchyme homeo box 2 (growth arrest-specific homeo box);

sine oculis homeobox homolog 1 (Drosophila);

crystallin, alpha B;

disheveled associated activator of morphogenesis 2;

DKFZP586B2420 protein;

similar to neuralin 1;

tetranectin (plasminogen binding protein);

src homology three (SH3) and cysteine rich domain;

cholesterol 25-hydroxylase;

runt-related transcription factor 3;

interleukin 11receptor, alpha;

procollagen C-endopeptidase enhancer;

frizzled homolog 7 (Drosophila);

hypothetical gene BC008967;

collagen, type VIII, alpha 1;

tenascin C (hexabrachion);

iroquois homeobox protein 5;

hephaestin;

integrin, beta 8;

synaptic vesicle glycoprotein 2;

neuroblastoma, suppression of tumorigenicity 1;

insulin-like growth factor binding protein 2, 36kDa;

Homo sapiens cDNA FLJ12280 fis, clone MAMMA1001744;

cytokine receptor-like factor 1;

potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4;

integrin, beta 7;

transcriptional co-activator with PDZ-binding motif (TAZ);

sine oculis homeobox homolog 2 (Drosophila);

KIAA1034 protein;

vesicle-associated membrane protein 5 (myobrevin);

EGF-containing fibulin-like extracellular matrix protein 1;

early growth response 3;

distal-less homeo box 5;

hypothetical protein FLJ20373;

aldo-keto reductase family 1, member C3 (3-alpha hydroxysteroid dehydrogenase, type II);

biglycan;

transcriptional co-activator with PDZ-binding motif (TAZ);

fibronectin 1;

proenkephalin;

integrin, beta-like 1(with EGF-like repeat domains);

Homo sapiens mRNA full length insert cDNA clone EUROIMAGE 1968422;

EphA3;

KIAA0367 protein;

natriuretic peptide receptor C/guanylate cyclase C (atrionatriuretic peptide receptor C);

hypothetical protein FLJ14054;

Homo sapiens mRNA;

cDNA DKFZp564B222 (from clone DKFZp564B222);

BCL2/adenovirus E1B 19kDa interacting protein 3-like;

AE binding protein 1;

cytochrome c oxidase subunit VIIa polypeptide 1 (muscle);

similar to neuralin 1;

B cell translocation gene 1;

hypothetical protein FLJ23191; and

DKFZp586L151.

17. The pharmaceutical composition of claim 1 wherein the cells produce each of CD10, CD13, CD44, CD73, CD90, PDGFr-alpha, PD-L2 and HLA-A,B,C.

18. The pharmaceutical composition of claim 1 wherein the cells do not produce any of CD31, CD34, CD45, CD80, CD86, CD141, CD178, B7-H2, HLA-G, and HLA-DR, DP,DQ.

19. The pharmaceutical composition of claim 1, wherein the cells comprise the following characteristics:

production of each of CD10, CD13, CD44, CD73, CD90, PDGFr-alpha, PD-L2 and HLA-A,B,C; and

lack of production of each of CD31, CD34, CD45, CD80, CD86, CD141, CD178, B7-H2, HLA-G, and HLA-DR,DP,DQ.

20. The pharmaceutical composition of claim 19, wherein the cells further comprise the following characteristics:

secretion of each of MCP-1, IL-6, IL-8, GCP-2, HGF, KGF, FGF, HB-EGF, BDNF, TPO, MIP1b, I309, MDC, RANTES, and TIMP1; and

lack of secretion of each of TGF-beta2, ANG2, PDGFbb, MIP1a, and VEGF, as detected by ELISA.