HSV vectors for delivery of NT3 and treatment of CIPN
Disclosed herein are compositions and methods for treating neuropathy, embodiments, HSV vectors are provided comprising nucleic acid molecules encoding neurotrophins, such as neurotrophin 3 (NT3).
1. A variant of herpes simplex virus (HSV) McKrae strain whose genome contains an alteration such that the variant fails to express one or more immediate early genes, wherein the genome comprises a nucleic acid molecule encoding a neurotrophin 3 polypeptide.
2. The variant of herpes simplex virus (HSV) McKrae strain according to claim 1 , wherein the variant fails to express a functional protein characterized by SEQ ID NO: 2.
3. The variant of herpes simplex virus (HSV) McKrae strain according to claim 1 , wherein the variant fails to express a functional protein characterized by SEQ ID NO: 16.
4. A composition comprising:
a vector comprising a variant of herpes simplex virus (HSV) McKrae strain whose genome contains an alteration such that the variant fails to express one or more immediate early genes, wherein the genome comprises a nucleic acid molecule encoding a neurotrophin 3 polypeptide; and
a pharmaceutically acceptable carrier.
5. The composition according to claim 4 , wherein,
the variant fails to express a functional protein characterized by SEQ ID NO: 2.
6. The composition according to claim 4 wherein, the variant fails to express a functional protein characterized by SEQ ID NO: 16.
7. The composition of claim 4 , wherein the vector further comprises a promoter operatively linked to a sequence encoding neurotrophin 3.
8. The composition of claim 7 wherein the vector further comprises an enhancer upstream of the promoter.
9. The composition of claim 8 , wherein the promoter is tissue specific.
10. The composition of claim 8 , wherein the promoter is neuron specific.
11. The composition of claim 7 wherein the promoter is a human cytomegalovirus (HCMV) promoter.
12. The composition of claim 7 wherein the promoter is a calcitonin gene-related peptide (CGRP) promoter.
13. The composition of claim 4 , wherein the vector comprises a bovine growth hormone (BGH) polyadenylation signal.
14. The composition of claim 4 , wherein the carrier is a polyol.
15. The composition of claim 4 , wherein the carrier is glycerol.
16. The composition of claim 4 , wherein the nucleic acid molecule encoding a neurotrophin 3 polypeptide is codon optimized.
17. A method of inhibiting the development or progression of neuropathy in a subject, the method comprising administering to the subject a vector comprising a variant of herpes simplex virus (HSV) McKrae strain whose genome contains an alteration such that the variant fails to express one or more immediate early genes, wherein the genome comprises a nucleic acid molecule encoding a neurotrophin 3 polypeptide.
18. The method according to claim 17 , wherein the variant fails to express a functional protein characterized by SEQ ID NO: 2.
19. The method according to claim 17 , wherein the variant fails to express a functional protein characterized by SEQ ID NO: 16.
20. A method of treating neuropathy in a subject, the method comprising administering to the subject a vector comprising a variant of herpes simplex virus (HSV) McKrae strain whose genome contains an alteration such that the variant fails to express one or more immediate early genes, wherein the genome comprises a nucleic acid molecule encoding a neurotrophin 3 polypeptide.
21. The method of treating neuropathy in a subject according to claim 20 , wherein the variant fails to express a functional protein characterized by SEQ ID NO: 2.
22. The method of treating neuropathy in a subject according to claim 20 , wherein the variant fails to express a functional protein characterized by SEQ ID NO: 16.
23. The method according to claim 20 , wherein the neuropathy is a peripheral neuropathy.
24. The method according to claim 20 , wherein the neuropathy is iatrogenic.
25. The method according to claim 20 , wherein the neuropathy is a result of a cancer treatment.
26. The method according to claim 20 , wherein the neuropathy is a result of chemotherapy.
27. The method according to claim 26 , wherein the chemotherapy comprises a platinum based chemotherapeutic.
28. The method according to claim 20 , wherein the vector is administered by contact with the skin of a subject.
29. The method according to claim 20 , wherein the vector is administered intradermally.
30. In a method of treating a subject having cancer with a chemotherapeutic agent, the improvement comprising administering to the subject a vector comprising a variant of herpes simplex virus (HSV) McKrae strain whose genome contains an alteration such that the variant fails to express one or more immediate early genes, wherein the genome comprises a nucleic acid molecule encoding a neurotrophin 3 polypeptide, wherein the vector is administered to promote tolerance against chemotherapy induced neuropathy.