BIFUNCTIONAL VECTORS ALLOWING BCL11A SILENCING AND EXPRESSION OF AN ANTI-SICKLING HBB AND USES THEREOF FOR GENE THERAPY OF B-HEMOGLOBINOPATHIES
The #β-hemoglobinopathies #β-thalassemia (BT) and sickle cell disease (SCD) are the most frequent genetic disorders worldwide. These diseases are caused by mutations causing reduced or abnormal synthesis of the β-globin chain of the adult hemoglobin (Hb) tetramer. Here, the inventors intend to improve HSC-based gene therapy for β-thalassemia and SCD by developing an innovative, highly infectious LV vector expressing a potent anti-sickling β-globin transgene and a second biological function either increasing fetal γ-globin expression (for β-thalassemia and SCD). More particularly, the inventors have designed a novel lentivirus (LV), which carry two different functions: βAS3 gene addition and gene silencing. This last strategy allows the re-expression of the fetal γ-globin genes (HBG1 and HBG2) and production of the endogenous fetal hemoglobin (HbF). Elevated levels of HbF and HbAS3 (Hb tetramer containing βAS3-globin) will benefit the β-hemoglobinopathy phenotype by increasing the total amount of β-like globin that will: (i) reduce the alpha precipitates and improve the alpha/non alpha ratio in β-thalassemia, and (ii) reduce the sickling in SCD. This combined strategy will improve the β-hemoglobinopathy phenotype at a lower vector copy number (VCN) per cell compared to a LV expressing the βAS3 alone.
1 . A nucleic acid molecule having the sequence as set forth in SEQ ID NO:1 wherein a sequence encoding for an artificial microRNA (amiR) suitable for reducing the expression of BCL11A, is inserted i) between the nucleotide at position 85 and the nucleotide 86 at position in SEQ ID NO:1 and/or ii) between the nucleotide at position 146 and the nucleotide at position 147 in SEQ ID NO:1.
2 . The nucleic acid molecule of claim 1 wherein the amiR comprises a shRNA that is embedded into a miRNA backbone.
3 . The nucleic acid molecule of claim 2 wherein the miRNA backbone is derived from miR-142, miR-155, miR-181 and/or miR-223.
4 . The nucleic acid molecule of claim 2 wherein the shRNA adopts a stem-loop structure wherein a stem region is formed by a guide strand and a passenger strand.
5 . The nucleic acid molecule of claim 4 wherein the sequence encoding for the guide strand comprises the sequence as set forth in SEQ ID NO: 2.
6 . The nucleic acid molecule of claim 4 wherein a loop segment is encoded by the sequence as set forth in SEQ ID NO:3.
7 . The nucleic acid molecule of claim 2 wherein the sequence encoding for the shRNA comprises the sequence as set forth in SEQ ID NO:4.
8 . The nucleic acid molecule of claim 1 wherein the sequence encoding for the amiR comprises the sequence as set forth in SEQ ID NO:5.
9 . The nucleic acid molecule of claim 1 that has a sequence as set forth in SEQ ID NO:6 or SEQ ID NO:7.
10 . A transgene encoding for an anti-sickling β-globin (HBB) wherein said transgene comprises the nucleic acid molecule of claim 1 .
11 . The transgene of claim 10 which comprises the sequence as set forth in SEQ ID NO:9 or SEQ ID NO:10.
12 . The transgene of claim 10 which is placed under the transcriptional control of the HBB promoter and key regulatory elements from the 16-kb human β-locus control region (βLCR), wherein the key regulatory elements comprise the 2 DNase I hypersensitive sites HS2 and HS3.
13 . A viral vector comprising the transgene of claim 10 .
14 . The viral vector of claim 13 which is a lentiviral vector.
15 . A method of obtaining a population of host cells transduced with the transgene of claim 10 , which comprises the step of transducing a population of host cells in vitro or ex vivo with the viral vector of claim 13 .
16 . The method of claim 15 wherein the host cell is selected from the group consisting of hematopoietic stem/progenitor cells, hematopoietic progenitor cells, hematopoietic stem cells (HSCs), pluripotent cells and induced pluripotent stem cells (iPS).
17 . A method of treating a hemoglobinopathy in a subject in need thereof, comprising transplanting into the subject a therapeutically effective amount of the population of host cells obtained by the method of claim 16 .
18 . The nucleic acid molecule of claim 1 , wherein the BCL11A is the BCL11A-XL isoform.
19 . The method of claim 16 wherein the pluripotent cells are embryonic stem cells (ES).