3D tissue-engineered bone marrow for personalized therapy and drug development
A tissue-engineered bone marrow for personalized therapy of a patient is described. The tissue-engineered bone marrow includes an autologous fibrin scaffold and a plurality of patient-derived cells isolated from the patient's bone marrow. The autologous fibrin scaffold is made using fibrinogen isolated from the patient's bone marrow. The plurality of patient-derived cells may include cells associated with a hematological or metastatic malignancy, bone marrow stromal cells, and endothelial cells. The patient-derived cells are cultured on the autologous fibrin scaffold to create the tissue-engineered bone marrow. The tissue-engineered bone marrow may be used for personalized drug screening.
1. A tissue-engineered bone marrow for personalized therapy of a patient comprising:
an autologous fibrin scaffold comprising fibrinogen isolated from the patient's bone marrow; and
a plurality of patient-derived cells isolated from the patient's bone marrow, comprising cells associated with a hematological or metastatic malignancy, wherein the cells associated with a hematological or metastatic malignancy are selected from acute lymphoblastic leukemia cells, acute myelogenous leukemia cells, chronic lymphocytic leukemia cells, acute monocytic leukemia cells, Hodgkin's lymphoma cells, non-Hodgkin's lymphoma cells, multiple myeloma cells, metastatic cells, and solid tumor cells,
wherein the patient-derived cells are cultured on the autologous fibrin scaffold.
2. The tissue-engineered bone marrow of claim 1 , wherein the autologous fibrin scaffold further comprises an antifibrinolytic agent.
3. The tissue-engineered bone marrow of claim 1 , wherein the autologous fibrin scaffold further comprises a patient-derived culture compound extracted from the patient's bone marrow, the patient-derived culture compound selected from the group consisting of: fibronectin, at least one growth factor, platelets, at least one cytokine, at least one enzyme, and combinations thereof.
4. The tissue-engineered bone marrow of claim 1 , further comprising a drug.
5. The tissue-engineered bone marrow of claim 4 , wherein the autologous fibrin scaffold further comprises a gradient of oxygen and a gradient of the drug.
6. The tissue-engineered bone marrow of claim 1 , wherein the cells associated with a hematological or metastatic malignancy are multiple myeloma cells.
7. A method of preparing a tissue-engineered bone marrow for personalized therapy of a patient comprising:
aspirating the patient's bone marrow;
separating a cellular fraction and a supernatant;
isolating a plurality of patient-derived cells from the cellular fraction, the patient-derived cells selected from the group consisting of cells associated with a hematological or metastatic malignancy, bone marrow stromal cells, endothelial cells, and combinations thereof;
creating an autologous fibrin scaffold comprising fibrinogen isolated from the supernatant; and
culturing the plurality of patient-derived cells on the fibrin scaffold.
8. The method of claim 7 , wherein the autologous fibrin scaffold further comprises an antifibrinolytic agent.
9. The method of claim 7 , wherein the autologous fibrin scaffold further comprises a patient-derived culture compound isolated from the supernatant, the patient-derived culture compound selected from the group consisting of: fibronectin, at least one growth factor, platelets, at least one cytokine, at least one enzyme, and combinations thereof.
10. The method of claim 7 , further comprising administering a dose of a drug to the tissue-engineered bone marrow.
11. The method of claim 10 , wherein the autologous fibrin scaffold further comprises a gradient of oxygen and a gradient of the drug.
12. The method of claim 7 , wherein the cells associated with a hematological or metastatic malignancy are selected from acute lymphoblastic leukemia cells, acute myelogenous leukemia cells, chronic lymphocytic leukemia cells, acute monocytic leukemia cells, Hodgkin's lymphoma cells, non-Hodgkin's lymphoma cells, multiple myeloma cells, metastatic cells, and solid tumor cells.