Phospholipid ether (PLE) CAR T cell tumor targeting (CTCT) agents
Aspects of the invention described herein relate to synthetic compounds that are useful for targeting and labeling tumor cells so as to facilitate recognition by binding agents including Chimeric Antigen Receptor T cells (CAR T cells), which are administered to a subject by intravenous or locoregional administration. Several compositions and methods of making and using these compositions to treat or inhibit a disease in a subject are contemplated.
1. A method of forming a complex between an effector cell and a target cell, the method comprising:
(a) contacting the target cell with a compound comprising a phospholipid, wherein the phospholipid comprises a hydrophobic group, a polar head group, and a target moiety, thereby obtaining a target cell comprising the target moiety; and
(b) contacting the target cell comprising the target moiety with the effector cell, wherein the effector cell comprises a chimeric antigen receptor (CAR), wherein the CAR specifically binds to the target moiety.
2. The method of claim 1 , wherein the compound further comprises a masking moiety, wherein the masking moiety is linked to the target moiety via a cleavable moiety.
3. The method of claim 2 , wherein the cleavable moiety is configured to be cleavable by a reactive oxygen species (ROS) or by an acidic environment.
4. The method of claim 1 , wherein the hydrophobic group comprises a fatty acid.
5. The method of claim 1 , wherein the hydrophobic group comprises a C 8-22 alkyl group.
6. The method of claim 1 , wherein the hydrophobic group comprises a terpenoid lipid.
7. The method of claim 1 , wherein the phospholipid comprises an ether linkage, wherein the ether linkage is between the polar head group and the hydrophobic group.
8. The method of claim 7 , wherein the phospholipid is a phospholipid ether (PLE).
9. The method of claim 1 , wherein the polar head comprises a group selected from phosphatidylcholine, sphingomyelin, phosphoethanolamine, phosphatidyl serine, phosphatidyl inositol, phosphocholine, or a trimethylarseno-ethyl-phosphate.
10. The method of claim 1 , wherein the phospholipid further comprises a spacer between the target moiety and the polar head group, wherein the spacer is selected from the group consisting of poly(carboxybetaine), peptide, polyglycidol, polyethylene, polyanhydride, polyphosphoester, polycaprolactone, polyethylene glycol (PEG), and an alkane chain.
11. The method of claim 10 , wherein the PEG spacer comprises from 1 to 21 PEG subunits.
12. The method of claim 1 , wherein the effector cell is a T cell.
13. The method of claim 1 , wherein the effector cell is selected from a precursor T cell, a hematopoietic stem cell, a CD8+ T cell, or a CD4+ T cell, a tumor cell, an immune cell, a T cell, or a B cell.
14. The method of claim 1 , wherein the target cell is a cancer cell.
15. The method of claim 14 , wherein the cancer cell is selected from a breast cancer cell, an ovarian cancer cell, a lung cancer cell, a pancreatic cancer cell, a prostate cancer cell, a melanoma cell, a renal cancer cell, a glioblastoma cell, a neuroblastoma cell, a medulloblastoma cell, a sarcoma cell, or a liver cancer cell.
16. The method of claim 1 , wherein the compound has the following structure:
wherein:
R is the target moiety;
n is 0 to 21; and
x is 8 to 22.
17. The method of claim 1 , wherein the target cell is in vivo.
18. The method of claim 1 , wherein the target cell is human.
19. The method of claim 16 , wherein:
the target cell is a neuroblastoma cell, a glioblastoma cell, a medulloblastoma cell, or a leukemia cell; and
the effector cell is a T cell.
20. A method of forming a complex between an effector cell and a target cell, the method comprising:
(a) contacting the target cell with a compound comprising a phospholipid, wherein the phospholipid comprises a target moiety, thereby obtaining a target cell comprising the target moiety, wherein the target cell is a non-solid tumor cell, and wherein the compound has the following structure:
wherein:
R is the target moiety,
n is 0 to 21, and
x is 8 to 22; and
(b) contacting the target cell comprising the target moiety with the effector cell, wherein the effector cell comprises a T cell, wherein the effector cell comprises a chimeric antigen receptor (CAR), and wherein the CAR specifically binds to the target moiety.