Composition and Method for Treating Diseases Thereof

Abstract

A composition and a method for treating diseases thereof are provided, wherein the composition comprises placental decidual mesenchymal stem cells, wherein the placental decidual mesenchymal stem cells overexpress decoy receptor 3 (DcR3) by stimulating with TNF-?, IFN-?, IL-6 or their combination thereof, and wherein the diseases including neurological diseases, eye diseases, and lung diseases.

Claims

1. A composition for treating neurological diseases, comprising placental decidual mesenchymal stem cells (DMSCs), wherein the placental decidual mesenchymal stem cells (DMSCs) overexpress decoy receptor 3 (DcR3) by stimulating with Tumor Necrosis Factor-? (TNF-?), Interferon-? (IFN-?), Interleukin-6 (IL-6) or their combination thereof.

2. The composition of claim 1, wherein the placental decidual mesenchymal stem cells (DMSCs) overexpress DcR3 is prepared by the following steps: culturing the DMSCs from human in a culture dish containing a serum-free medium until the DMSCs from human adhere to the culture dish; adding at least one inflammatory cytokine at an effective amount to the culture dish containing a serum-free medium, wherein the at least one inflammatory cytokine is Tumor Necrosis Factor-? (TNF-?), Interferon-? (IFN-?), Interleukin-6 (IL-6), or their combination thereof; allowing the at least one inflammatory cytokine to stimulate expression of DcR3 in the DMSCs from human for 48 hours; and obtaining the DMSCs from human having increased expression level of DcR3 compared to DMSCs from human cultured without the stimulation of the at least one inflammatory cytokine, wherein the increased in statistically significant with a P value of less than 0.05.

3. The composition of claim 1, wherein the neurological diseases comprise neuroinflammation related disease or apoptosis of nerve cells.

4. The composition of claim 1, wherein the neurological diseases comprise stroke, trauma, Alzheimer's disease (AD), Parkinson's disease (PD), Multiple Sclerosis (MS), spinal cord injury, or peripheral nerve injury.

5. A method for treatment of neurological diseases, comprising administering a composition comprises placental decidual mesenchymal stem cells (DMSCs) to a subject in need thereof, wherein the placental decidual mesenchymal stem cells (DMSCs) overexpress decoy receptor 3 (DcR3) by stimulating with Tumor Necrosis Factor-? (TNF-?), Interferon-? (IFN-?), Interleukin-6 (IL-6), or their combination thereof.

6. The method of claim 5, wherein the placental decidual mesenchymal stem cells (DMSCs) overexpress DcR3 is prepared by the following steps: culturing the DMSCs from human in a culture dish containing a serum-free medium until the DMSCs from human adhere to the culture dish; adding at least one inflammatory cytokine at an effective amount to the culture dish containing a serum-free medium, wherein the at least one inflammatory cytokine is Tumor Necrosis Factor-? (TNF-?), Interferon-? (IFN-?), Interleukin-6 (IL-6), or their combination thereof; allowing the at least one inflammatory cytokine to stimulate expression of DcR3 in the DMSCs from human for 48 hours; and obtaining the DMSCs from human having increased expression level of DcR3 compared to DMSCs from human cultured without the stimulation of the at least one inflammatory cytokine, wherein the increased in statistically significant with a P value of less than 0.05.

7. The method of claim 5, wherein the neurological diseases comprise neuroinflammation related disease or apoptosis of nerve cells.

8. The method of claim 5, wherein the neurological diseases comprise stroke, trauma, Alzheimer's disease (AD), Parkinson's disease (PD), Multiple Sclerosis (MS), spinal cord injury, or peripheral nerve injury.

9. A composition for treating eye diseases, comprising placental decidual mesenchymal stem cells (DMSCs), wherein the placental decidual mesenchymal stem cells (DMSCs) overexpress decoy receptor 3 (DcR3) by stimulating with Tumor Necrosis Factor-? (TNF-?), Interferon-? (IFN-?), Interleukin-6 (IL-6), or their combination thereof.

10. The composition of claim 9, wherein the placental decidual mesenchymal stem cells (DMSCs) overexpress DcR3 is prepared by the following steps: culturing the DMSCs from human in a culture dish containing a serum-free medium until the DMSCs from human adhere to the culture dish; adding at least one inflammatory cytokine at an effective amount to the culture dish containing a serum-free medium, wherein the at least one inflammatory cytokine is Tumor Necrosis Factor-? (TNF-?), Interferon-? (IFN-?), Interleukin-6 (IL-6), or their combination thereof; allowing the at least one inflammatory cytokine to stimulate expression of DcR3 in the DMSCs from human for 48 hours; and obtaining the DMSCs from human having increased expression level of DcR3 compared to DMSCs from human cultured without the stimulation of the at least one inflammatory cytokine, wherein the increased in statistically significant with a P value of less than 0.05.

11. The composition of claim 9, wherein the eye diseases comprise dry eye, cataract, glaucoma, cornea inflammation, conjunctivitis or age-related macular degeneration (AMD).

12. A method for treatment of eye diseases, comprising administering a composition comprises placental decidual mesenchymal stem cells (DMSCs) to a subject in need thereof, wherein the placental decidual mesenchymal stem cells (DMSCs) overexpress decoy receptor 3 (DcR3) by stimulating with Tumor Necrosis Factor-? (TNF-?), Interferon-? (IFN-?), Interleukin-6 (IL-6), or their combination thereof.

13. The method of claim 12, wherein the placental decidual mesenchymal stem cells (DMSCs) overexpress DcR3 is prepared by the following steps: culturing the DMSCs from human in a culture dish containing a serum-free medium until the DMSCs from human adhere to the culture dish; adding at least one inflammatory cytokine at an effective amount to the culture dish containing a serum-free medium, wherein the at least one inflammatory cytokine is Tumor Necrosis Factor-? (TNF-?), Interferon-? (IFN-?), Interleukin-6 (IL-6), or their combination thereof; allowing the at least one inflammatory cytokine to stimulate expression of DcR3 in the DMSCs from human for 48 hours; and obtaining the DMSCs from human having increased expression level of DcR3 compared to DMSCs from human cultured without the stimulation of the at least one inflammatory cytokine, wherein the increased in statistically significant with a P value of less than 0.05.

14. The method of claim 12, wherein the eye diseases comprise dry eye, cataract, glaucoma, cornea inflammation, conjunctivitis or age-related macular degeneration (AMD).

15. A composition for treating lung diseases, comprising placental decidual mesenchymal stem cells (DMSCs), wherein the placental decidual mesenchymal stem cells (DMSCs) overexpress decoy receptor 3 (DcR3) by stimulating with Tumor Necrosis Factor-? (TNF-?), Interferon-? (IFN-?), Interleukin-6 (IL-6), or their combination thereof.

16. The composition of claim 15, wherein the placental decidual mesenchymal stem cells (DMSCs) overexpress DcR3 is prepared by the following steps: culturing the DMSCs from human in a culture dish containing a serum-free medium until the DMSCs from human adhere to the culture dish; adding at least one inflammatory cytokine at an effective amount to the culture dish containing a serum-free medium, wherein the at least one inflammatory cytokine is Tumor Necrosis Factor-? (TNF-?), Interferon-? (IFN-?), Interleukin-6 (IL-6), or their combination thereof; allowing the at least one inflammatory cytokine to stimulate expression of DcR3 in the DMSCs from human for 48 hours; and obtaining the DMSCs from human having increased expression level of DcR3 compared to DMSCs from human cultured without the stimulation of the at least one inflammatory cytokine, wherein the increased in statistically significant with a P value of less than 0.05.

17. The composition of claim 15, wherein the lung diseases comprise pneumonia, chronic obstructive pulmonary disease (COPD), acute lung injury (ALI) or acute respiratory distress syndrome (ARDS).

18. A method for treatment of lung diseases, comprising administering a composition comprises placental decidual mesenchymal stem cells (DMSCs) to a subject in need thereof, wherein the placental decidual mesenchymal stem cells (DMSCs) overexpress decoy receptor 3 (DcR3) by stimulating with Tumor Necrosis Factor-? (TNF-?), Interferon-? (IFN-?), Interleukin-6 (IL-6), or their combination thereof.

19. The method of claim 18, wherein the placental decidual mesenchymal stem cells (DMSCs) overexpress DcR3 is prepared by the following steps: culturing the DMSCs from human in a culture dish containing a serum-free medium until the DMSCs from human adhere to the culture dish; adding at least one inflammatory cytokine at an effective amount to the culture dish containing a serum-free medium, wherein the at least one inflammatory cytokine is Tumor Necrosis Factor-? (TNF-?), Interferon-? (IFN-?), Interleukin-6 (IL-6), or their combination thereof; allowing the at least one inflammatory cytokine to stimulate expression of DcR3 in the DMSCs from human for 48 hours; and obtaining the DMSCs from human having increased expression level of DcR3 compared to DMSCs from human cultured without the stimulation of the at least one inflammatory cytokine, wherein the increased in statistically significant with a P value of less than 0.05.

20. The composition of claim 18, wherein the lung diseases comprise pneumonia, chronic obstructive pulmonary disease (COPD), acute lung injury (ALI) or acute respiratory distress syndrome (ARDS).

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0025] FIG. 1 shows the survival rate of mouse with the treatment of bone-marrow mesenchymal stem cells and placental decidual mesenchymal stem cells. The results indicate that , 12%, 38% ?

EMBODIMENTS

[0026] To make the above-described and other purposes, features, and advantages of the present invention more obvious and easier to understand, preferred embodiments are provided below, and are described in detail as follows:

EXAMPLE 1

Methods

[0027] (1) ( TNF-?, IFN-?, IL-6) 24?72 [0028] (2) ( TNF-?, IFN-?, IL-6) , , , , [0029] (3) , anti-DcR3 antibody DcR3 , anti-DcR3 antibody ,

Results

[0030]

[0031] , ,

[0032] anti-DcR3 antibody , ,

Conclusion

[0033] , DcR3, ,

EXAMPLE 2

Methods

[0034] (1) ( TNF-?, IFN-?, IL-6) 24?72 [0035] (2) ( TNF-?, IFN-?, IL-6) , , , , [0036] (3) (2) , anti-DcR3 antibody DcR3 , anti-DcR3 antibody ,

Results

[0037]

[0038] , ,

[0039] anti-DcR3 antibody , ,

Conclusion

[0040] , DcR3, ,

EXAMPLE 3

Methods

[0041] (1) ( TNF-?, IFN-?, IL-6) 24?72 [0042] (2) ( TNF-?, IFN-?, IL-6) , , , , [0043] (3) (2) , anti-DcR3 antibody DcR3 , anti-DcR3 antibody , [0044] (4) , DcR3 DcR3

Results

[0045]

[0046] , ,

[0047] anti-DcR3 antibody , ,

[0048] , DcR3 ,

Conclusion

[0049] , DcR3, ,

[0050] While the invention has been described and exemplified in sufficient detail for those skilled in this art to make and use it, various alternatives, modifications, and improvements should be apparent without departing from the spirit and scope of the invention.

[0051] One skilled in the art readily appreciates that the present invention is well adapted to carry out the objects and obtain the ends and advantages mentioned, as well as those inherent therein. The cells, animals, and processes and methods for producing them are representative of preferred embodiments, are exemplary, and are not intended as limitations on the scope of the invention. Modifications therein and other uses will occur to those skilled in the art. These modifications are encompassed within the spirit of the invention and are defined by the scope of the claims.