Constitutively active cytokine receptors for cell therapy
Embodiments of the disclosure include methods and compositions for enhancing expansion of immune cells for immunotherapy. In particular embodiments, immune cells, such as T-cells, express a constitutively active cytokine receptor in which the transmembrane and endodomains are able to provide an activating signal separately from any input to the corresponding exodomain to which they are operably linked. In specific embodiments, the transmembrane and endodomain from IL-7Rα is utilized with the exodomain of CD34.
1. A polynucleotide that encodes an engineered constitutively active receptor polypeptide, said polypeptide comprising the following components:
a) an TL-7 cytokine receptor alpha chain endodomain;
b) a transmembrane domain comprises the sequence selected from the group consisting of SEQ ID NO:2, SEQ ID NO:3, SEQ ID NO:4, SEQ ID NO:5, SEQ ID NO:6, SEQ ID NO:7, SEQ ID NO:8, SEQ ID NO:9, SEQ ID NO:10, SEQ ID NO:11, SEQ ID NO:12, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:15, SEQ ID NO:16, SEQ ID NO:17, SEQ ID NO:18, SEQ ID NO:19, SEQ ID NO:20, SEQ ID NO:21, SEQ ID NO:22, SEQ ID NO:23, and SEQ ID NO:24; and
c) one or more extracellular domains, wherein the extracellular domain is from PD-1, B7, CD30, HER2, EGFR, CD19, CD34, TGF-beta receptor, IL-4 receptor, IL-13 receptor alpha1 and alpha 2, IL-8 receptor, IL-10 receptor, LAG3, TIGIT, CTLA4, FAS, CD27, CD28, CD52, CD134, CD137, or NGFR.
2. A cell comprising the polynucleotide of claim 1 .
3. The cell of claim 2 , wherein the transmembrane domain is self-oligomerizing.
4. The cell of claim 2 , wherein the extracellular domain is globular in form.
5. The cell of claim 2 , wherein the extracellular domain comprises an extracellular domain from PD-1 or B7.
6. The cell of claim 2 , wherein the extracellular domain is the extracellular domain of CD34.
7. The cell of claim 2 , wherein the length of the extracellular domain, except CD52, is at least 70 amino acids.
8. The cell of claim 2 , wherein the length of the extracellular domain is no more than 2000 amino acids.
9. The cell of claim 2 , wherein the length of the extracellular domain is between 70-2000 amino acids.
10. The cell of claim 2 , wherein the cell is an immune cell.
11. The cell of claim 2 , wherein the cell is a T-cell, a NK cell, a NKT cell, αβ cell, γδ T-cell, a Mucosa Associated Invariant T-cell (MAIT T-cell), innate lymphoid cell, a stem cell, or a progenitor cell.
12. The cell of claim 2 , wherein the cell comprises a non-natural molecule that confers antigen specificity for the cell.
13. The cell of claim 2 , wherein the cell further comprises at least one additional engineered receptor.
14. The cell of claim 13 , wherein the additional engineered receptor is a constitutively active cytokine receptor, a chimeric antigen receptor, a recombinant T-cell receptor, a bispecific T-cell engager, Dual-Affinity Re-Targeting protein, or a combination thereof.
15. The cell of claim 2 , wherein the cell is a T-cell that comprises at least one chimeric antigen receptor.
16. The cell of claim 2 , wherein the polynucleotide further comprises an expression vector.
17. The cell of claim 16 , wherein the expression vector is a viral vector or a non-viral vector.
18. The cell of claim 17 , wherein the viral vector is a retroviral, lentiviral, adenoviral, or adeno-associated viral vector.
19. A plurality of cells of claim 2 , wherein the cells comprise a mixture of one or more of a T-cell, a NK cell, a NKT cell, an αβ T-cell, a γδ T-cell, a Mucosa Associated Invariant T-cell (MAIT T-cell), innate lymphoid cell, a stem cell, or a progenitor cell.
20. A plurality of cells of claim 2 , wherein the cells comprise one or more immune effector cells.
21. The cell of claim 2 , wherein the length of the extracellular domain is between 50-500 amino acids.