Luteinizing hormone receptor binding agents and luteinizing hormone agonists to identify, expand, ablate and modify stem cells
The use of luteinizing hormone receptor (LHR) binding agents and luteinizing hormone (LH) agonists to enrich for primitive hematopoietic stem cell (pHSC) populations, to target pHSC for ablation, and/or to expand pHSC populations are described. The methods can be used to prepare therapeutic hematopoietic stem cell (HSC) populations, to prepare patients for therapeutic HSC transplants, and/or to treat malignancies, such as those associated with hyperproliferative HSC.
1. A chimeric antigen receptor (CAR) comprising an extracellular domain linked to an intracellular signaling domain through a transmembrane domain wherein the extracellular domain comprises a luteinizing hormone (LH) alpha subunit and a LH beta subunit,
wherein the LH alpha subunit comprises the sequence set forth in SEQ ID NO: 23 or a sequence having at least 90% sequence identity to the sequence set forth in SEQ ID NO: 23 and the LH beta subunit comprises the sequence set forth in SEQ ID NO: 22 or a sequence having at least 90% sequence identity to the sequence set forth in SEQ ID NO: 22 or
the LH alpha subunit comprises the sequence set forth in SEQ ID NO: 11 or a sequence having at least 90% sequence identity to the sequence set forth in SEQ ID NO: 11 and the LH beta subunit comprises the sequence set forth in SEQ ID NO: 9 or a sequence having at least 90% sequence identity to the sequence set forth in SEQ ID NO: 9,
and wherein the LH alpha subunit and the LH beta subunit bind the LH receptor.
2. The CAR of claim 1 , wherein the LH alpha subunit and the LH beta subunit are linked by a sequence set forth in SEQ ID NO: 10 or a sequence having at least 90% sequence identity to the sequence set forth in SEQ ID NO: 10.
3. The CAR of claim 1 , wherein the intracellular signaling domain comprises a CD3 zeta sequence set forth in SEQ ID NO: 27 or SEQ ID NO: 16.
4. The CAR of claim 1 , comprising
the sequence set forth in SEQ ID NO: 20 or a sequence having at least 90% sequence identity to SEQ ID NO: 20 or
the sequence set forth in SEQ ID NO: 7 or a sequence having at least 90% sequence identity to SEQ ID NO: 7.
5. The CAR of claim 1 , further comprising a tag sequence within the extracellular domain.
6. The CAR of claim 5 , wherein the tag sequence comprises Myc tag, Strep tag, His tag, Flag tag, Xpress tag, Avi tag, Calmodulin tag, Polyglutamate tag, HA tag, or V5 tag.
7. An immune cell expressing a CAR of claim 1 .
8. The immune cell of claim 7 , wherein the immune cell is a pHSC, HSC, T cell or NK cell.
9. The CAR of claim 1 , wherein the extracellular domain further comprises a CD28 hinge sequence.
10. The CAR of claim 1 , wherein the transmembrane domain comprises a CD28 transmembrane domain sequence.
11. The CAR of claim 10 , wherein the CD28 transmembrane domain sequence comprises the sequence set forth in SEQ ID NO: 25.
12. The CAR of claim 1 , wherein the intracellular signaling domain comprises a 4-1BB sequence.
13. The CAR of claim 12 , wherein the 4-1BB sequence comprises the sequence set forth in SEQ ID NO: 26.
14. The CAR of claim 1 , wherein the intracellular signaling domain comprises a CD3 zeta sequence.
15. The CAR of claim 1 , wherein the intracellular signaling domain comprises a CD28 cytoplasmic sequence.
16. The CAR of claim 1 , wherein the intracellular signaling domain comprises a CD3 zeta sequence.
17. The CAR of claim 1 , further comprising a linker within the extracellular domain that is 16 amino acids or less.
18. The CAR of claim 17 , wherein the linker is a Gly-Ser linker.
19. The CAR of claim 18 , wherein the Gly-Ser linker comprises the sequence set forth in SEQ ID NO: 10.