Therapeutic retroviral vectors for gene therapy
The invention provides improved compositions and methods for achieving gene therapy in hematopoietic cells and hematopoietic precursor cells, including erythrocytes, erythroid progenitors, and embryonic stem cells. The invention further provides improved gene therapy methods for treating hematopoietic-related disorders. Retroviral gene therapy vectors that are optimized for erythroid specific expression and treatment of hemoglobinopathic conditions are disclosed.
1. A self-inactivating (SIN) lentiviral vector comprising:
a) a human immunodeficiency virus 1 (HIV-1) 5′ long terminal repeat (LTR), wherein the promoter of the HIV-1 5′ LTR is replaced with a CMV promoter;
b) an RNA export element;
c) a central polypurine tract or DNA FLAP (cPPT/FLAP);
d) a β-globin promoter;
e) a β-globin locus control region (LCR), wherein the β-globin promoter and β-globin LCR are operatively linked to a polynucleotide encoding a human globin; and
f) a HIV-1 3′ LTR, wherein the 3′ LTR comprises at least one deletion compared to the wild-type HIV-1 3′ LTR.
2. The SIN lentiviral vector of claim 1 , wherein the HIV-1 5′ LTR further comprises a deletion compared to the wild-type HIV-1 5′ LTR.
3. The SIN lentiviral vector of claim 1 , wherein the RNA export element comprises a hepatitis B virus post-transcriptional regulatory element (PRE) or a human immunodeficiency virus (HIV) rev response element (RRE).
4. The SIN lentiviral vector of claim 1 , wherein the HIV-1 3′ LTR comprises a polyadenylation sequence.
5. The SIN lentiviral vector of claim 1 , wherein the β-globin LCR comprises DNase I hypersensitive sites 2, 3, and 4 from the human β-globin LCR.
6. The SIN lentiviral vector of claim 1 , further comprising a human β-globin 3′ enhancer element.
7. The SIN lentiviral vector of any one of claims 1 - 6 , wherein the SIN lentiviral vector does not comprise an insulator element.
8. The SIN lentiviral vector of claim 1 , wherein the polynucleotide encodes a human β-globin, a human δ-globin, a human γ-globin, or a human β A-T87Q -globin.
9. The SIN lentiviral vector of claim 1 , further comprising a nucleic acid cassette comprising a suicide gene operably linked to a promoter or a gene for in vivo selection of the cell.
10. The vector of claim 9 , wherein the suicide gene is herpes simplex virus thymidine kinase (HSV-Tk).
11. The vector of claim 9 , wherein the gene for in vivo selection is methylguanine methyltransferase (MGMT).
12. A SIN lentiviral vector comprising:
a) an HIV-1 5′ LTR, wherein the promoter of the HIV-1 5′ LTR is replaced with a CMV promoter;
b) an RRE;
c) a cPPT/FLAP;
d) a β-globin promoter;
e) a β-globin locus control region (LCR), wherein the β-globin promoter and β-globin LCR are operatively linked to a polynucleotide encoding a human anti-sickling β-globin; and
f) a HIV-1 3′ LTR, wherein the 3′ LTR comprises at least one deletion compared to the wild-type HIV-1 3′ LTR.
13. A SIN lentiviral vector comprising:
a) an HIV-1 5′ LTR, wherein the promoter of the HIV-1 5′ LTR is replaced with a CMV promoter;
b) an RRE;
c) a cPPT/FLAP;
d) a β-globin promoter;
e) a β-globin locus control region (LCR), wherein the β-globin promoter and β-globin LCR are operatively linked to a polynucleotide encoding a human β-globin comprising a threonine to glutamine mutation at codon 87;
f) a human β-globin 3′ enhancer element; and
g) a HIV-1 3′ LTR, wherein the 3′ LTR comprises at least one deletion compared to the wild-type HIV-1 3′ LTR.
14. A cell transduced with the SIN lentiviral vector of claim 13 .
15. The transduced cell of claim 14 , wherein the cell is an embryonic stem cell, a somatic stem cell, or a progenitor cell.
16. The transduced cell of claim 14 , wherein the cell is a bone marrow cell, a hematopoietic stem cell, or a hematopoietic progenitor cell.
17. The transduced cell of claim 14 , wherein the cell is an erythrocyte.