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New Indications for BMT: Extracellular Matrix Disorder Dystrophic Epidermolysis Bullosa from Jakub Tolar, MD, PhD Blood and Marrow Transplantation University.

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Presentation on theme: "New Indications for BMT: Extracellular Matrix Disorder Dystrophic Epidermolysis Bullosa from Jakub Tolar, MD, PhD Blood and Marrow Transplantation University."— Presentation transcript:

1 New Indications for BMT: Extracellular Matrix Disorder Dystrophic Epidermolysis Bullosa from Jakub Tolar, MD, PhD Blood and Marrow Transplantation University of Minnesota

2 Collagen Type VII = Anchoring Fibrils Anchoring Fibrils = VELCRO

3 To determine whether systemically administered hematopietic cells can correct collagen type VII deficiency in recessive dystrophic epidermolysis bullosa.

4 C7 protein expression adjacent to donor cells in murine model of EB Collagen type VII Donor cell Tolar J, et al. Blood 2009;113:1167-74

5 Clinical Trial. -9-8-7-6-5-4-3-2-1 0 CYCLOPHOSPHAMIDE Transplant FLUDARABINE MYCOPHENYLATE CYCLOSPORINE BUSULPHAN Skin Evaluations at days 0, 28, 60, 100, 6 months, 1 and 2 years 1.Photographs of skin and oral mucosa 2.Collagen type VIIimmunofluorescence 3.Electron microscopy (evaluated by blinded reviewers) Days -9-8-7-6-5-4-3-2-1 0 CYCLOPHOSPHAMIDE Transplant FLUDARABINE MYCOPHENYLATE CYCLOSPORINE BUSULPHAN Skin Evaluations at days 0, 28, 60, 100, 6 months, 1 year, and 2 years 1.Photographs of skin and oral mucosa 2.Collagen type VIIimmunofluorescence 3.Electron microscopy (evaluated by blinded reviewers) Days Clinical Trial for RDEB Eligibility 1. Dx of RDEB 2. 0-25 years 3. Adequate donor 4. Acceptable organ function 5. No SCC

6 Transplant Improves Skin Blistering Before After BeforeAfter

7 Transplant Increases Collagen 7 Before After

8 Non-hematopoietic male donor cells Dermal- epidermal junction Hematopoietic male donor cells Collagen 7 Blood vessel Donor non-hematopoietic cells in epidermis and dermis after HCT

9 Summary Adoptive transfer of bone marrow and cord blood cells results in functional correction of recessive dystrophic epidermolysis bullosa.

10 Clinical Trial. -9-8-7-6-5-4-3-2-1 0 CYCLOPHOSPHAMIDE Transplant FLUDARABINE MYCOPHENYLATE CYCLOSPORINE BUSULPHAN Skin Evaluations at days 0, 28, 60, 100, 6 months, 1 and 2 years 1.Photographs of skin and oral mucosa 2.Collagen type VIIimmunofluorescence 3.Electron microscopy (evaluated by blinded reviewers) Days -9-8-7-6-5-4-3-2-1 0 CYCLOPHOSPHAMIDE HSC+MSC FLUDARABINE MYCOPHENYLATE CYCLOSPORINE BUSULPHAN Skin Evaluations at days 0, 28, 60, 100, 6 months, 1 year, and 2 years 1.Photographs of skin and oral mucosa 2.Collagen type VIIimmunofluorescence 3.Electron microscopy Days Clinical Trial II for RDEB Eligibility 1. Dx of RDEB 2. 0-25 years 3. Adequate donor 4. Acceptable organ function 5. No SCC


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