Systemic targeting of inflammatory sites and enhanced immunomodulatory function by introducing the chimeric antigen receptor (CAR) into mesenchymal stem cells for inflammatory and autoimmune diseases
Mesenchymal stromal cells are engineered to express a chimeric antigen receptor (CAR), that specifically binds a marker of activated myeloid cells, including without limitation folate receptor beta; and are administered to an individual for treatment of inflammation at sites characterized by the presence of activated myeloid cells.
1. A method for treating an inflammatory condition in a subject in need thereof, comprising administering to said subject:
an effective dose of mesenchymal stromal cells (MSC) engineered to express a chimeric antigen receptor (iCAR) that specifically binds folate receptor beta (FRβ); wherein the MSC has been further engineered to express an anti-inflammatory cytokine
wherein inflammation is decreased at the targeted site.
2. The method of claim 1 , wherein the cytokine is one or both of IL4 and IL-13.
3. The method of claim 1 , wherein the cytokine is expressed as a fusion protein linked to the iCAR by a cleavable peptide.
4. The method of claim 1 , wherein the cytokine is expressed independently of the CAR.
5. The method of claim 4 , wherein cytokine expression is regulated.
6. The method of claim 1 , wherein the iCAR directly binds to FRβ.
7. The method of claim 1 , wherein the MSC cells are autologous.
8. The method of claim 1 , wherein the MSC cells are allogeneic.
9. The method of claim 7 , wherein the MSC are engineered and expanded in culture.
10. The method of claim 1 , wherein the subject is a human.
11. The method of claim 1 , where the inflammatory condition is diabetes.
12. A method for treating an inflammatory condition in a subject in need thereof, comprising administering to said subject:
an effective dose of mesenchymal stromal cells (MSC) engineered to express a chimeric antigen receptor (iCAR) that specifically binds folate receptor beta (FRβ); administered in combination with an effective dose of targeting antibodies, which antibodies (i) bind to FRβ and (ii) are labeled with the non-endogenous antigenic moiety.