Compositions and methods related to engineered erythoid cells comprising 4-1BBL
The invention includes compositions and methods related to multimodal therapies, e.g., for treating a cancer. A multimodal therapy described herein provides and/or administers a plurality of agents that function in a coordinated manner to provide a therapeutic benefit to a subject in need thereof, e.g., a subject having a cancer.
1. A genetically engineered enucleated erythroid cell comprising an exogenous polypeptide comprising a 4-1BB-binding fragment of 4-1BBL at the surface of the genetically engineered enucleated erythroid cell,
wherein the enucleated erythroid cell was produced by a process comprising:
introducing an exogenous nucleic acid encoding the exogenous polypeptide into a nucleated erythroid cell, or a precursor thereof; and
culturing the nucleated erythroid cell under conditions suitable for enucleation and for production of the exogenous polypeptide.
2. The genetically engineered enucleated erythroid cell of claim 1 , wherein the exogenous polypeptide further comprises a transmembrane domain.
3. The genetically engineered enucleated erythroid cell of claim 2 , wherein the transmembrane domain comprises a polypeptide having at least 80% identity to the amino acid sequence of SEQ ID NO: 9.
4. The genetically engineered enucleated cell of claim 1 , wherein the exogenous polypeptide comprises a 4-1BB-binding fragment of an amino acid sequence of SEQ ID NO: 21.
5. The genetically engineered enucleated erythroid cell of claim 1 , wherein the exogenous polypeptide lacks a sortase transfer signature.
6. The genetically engineered enucleated erythroid cell of claim 1 , which comprises a plurality of exogenous fusion proteins on the surface of the genetically engineered enucleated erythroid cell, wherein at least 50% of the exogenous fusion proteins comprised by the cell have an identical sequence.
7. The genetically engineered enucleated erythroid cell of claim 1 , which is a reticulocyte.
8. A method of treating cancer, comprising administering the genetically engineered enucleated erythroid cell of claim 1 to a subject in need thereof.
9. The method of claim 8 , wherein the cancer is selected from lung cancer, NSCLC, esophageal cancer, bladder cancer, stomach cancer, head and neck cancer, colorectal cancer, uterine cancer, cervical cancer, breast cancer, prostate cancer, ovarian cancer, liver cancer, kidney cancer, myeloma, and non-Hodgkin lymphoma.
10. The genetically engineered enucleated erythroid cell of claim 2 , wherein the transmembrane domain comprises a type I red blood cell transmembrane domain.
11. The genetically engineered enucleated erythroid cell of claim 2 , wherein the transmembrane domain comprises a type II red blood cell transmembrane domain.
12. The genetically engineered enucleated erythroid cell of claim 1 , which is capable of promoting T cell proliferation.
13. The genetically engineered enucleated erythroid cell of claim 1 , wherein the transmembrane domain comprises a glycophorin A (GPA) transmembrane domain.
14. The genetically engineered enucleated erythroid cell of claim 1 , which further comprises a second exogenous protein.
15. The genetically engineered enucleated erythroid cell of claim 1 , wherein the culturing comprises expanding the nucleated erythroid cell at least 1,000-fold.
16. A population of cells comprising a plurality of genetically engineered enucleated erythroid cells of claim 1 , wherein at least 60% of cells in the population are enucleated erythroid cells.
17. The population of claim 16 , wherein at least 90% of cells in the population are enucleated erythroid cells.
18. The population of claim 16 , wherein at least 80% of cells in the population are enucleated erythroid cells that comprise the exogenous polypeptide.
19. A pharmaceutical preparation comprising a plurality of genetically engineered enucleated erythroid cells of claim 1 .
20. The genetically engineered enucleated erythroid cell of claim 1 , wherein the precursor is a CD34+ cell.