Gene therapy for treating hemophilia A
Compositions and regimens useful in treating hemophilia A are provided. The compositions include recombinant adeno-associated virus (rAAV) with a transthyretin enhancer and promoter driving expression of a human Factor VIII.
1. A recombinant adeno-associated virus (rAAV) useful as a liver-directed therapeutic for hemophilia A, said rAAV comprising an AAV capsid, and a vector genome packaged therein, said vector genome comprising:
(a) an AAV 5′ inverted terminal repeat (ITR) sequence;
(b) a transthyretin enhancer (enTTR) comprising the nucleotide sequence as set forth in SEQ ID NO: 5;
(c) a transthyretin (TTR) promoter consisting of the nucleotide sequence as set forth in SEQ ID NO: 7;
(d) a coding sequence encoding a human Factor VIII having coagulation function,
wherein the coding sequence comprises the nucleotide sequence as set forth in SEQ ID NO: 2;
(e) a polyA sequence; and
(f) an AAV 3′ ITR sequence,
wherein the coding sequence of (d) is operably linked to expression control elements that consist of the enTTR, the TTR promoter, and the polyA sequence.
2. The rAAV according to claim 1 , wherein the human Factor VIII is a B-domain deleted factor VIII SQ which is about 1457 amino acid residues in length.
3. The rAAV according to claim 1 , wherein the AAV capsid is an hu37 capsid.
4. The rAAV according to claim 1 , wherein the AAV 5′ ITR sequence and/or the AAV 3′ ITR sequence is from AAV2.
5. The rAAV according to claim 1 , wherein the polyA sequence is about 75 bp in length.
6. The rAAV according to claim 1 , wherein the vector genome is 5 kilobases to 5.5 kilobases in size.
7. An aqueous suspension suitable for administration to a hemophilia A patient, said suspension comprising an aqueous suspending liquid and an effective amount of a recombinant adeno-associated virus (rAAV) useful as a liver-directed therapeutic for hemophilia A, said rAAV having an AAV capsid, and having packaged therein a vector genome comprising:
(a) an AAV 5′ inverted terminal repeat (ITR) sequence;
(b) a transthyretin enhancer (enTTR) comprising the nucleotide sequence as set forth in SEQ ID NO: 5;
(c) a transthyretin (TTR) promoter consisting of the nucleotide sequence as set forth in SEQ ID NO: 7;
(d) a coding sequence encoding a human Factor VIII having coagulation function,
wherein the coding sequence comprises the nucleotide sequence as set forth in SEQ ID NO: 2;
(e) a polyA sequence; and
(f) an AAV 3′ ITR sequence,
wherein the coding sequence of (d) is operably linked to expression control elements that consist of the enTTR, the TTR promoter, and the polyA sequence.
8. The aqueous suspension according to claim 7 , wherein the suspension is suitable for intravenous injection.
9. The aqueous suspension according to claim 7 , wherein the suspension further comprises a surfactant, preservative, and/or buffer dissolved in the aqueous suspending liquid.
10. The rAAV according to claim 1 , wherein the vector genome comprises nucleotides 1-5110 of the nucleotide sequence as set forth in SEQ ID NO: 13.
11. The rAAV according to claim 10 , wherein the AAV capsid is an hu37 capsid.
12. The rAAV according to claim 1 , wherein the AAV 5′ ITR sequence comprises the nucleotide sequence as set forth in SEQ ID NO: 11 and the AAV 3′ ITR sequence comprises the nucleotide sequence as set forth in SEQ ID NO: 12.
13. The rAAV according to claim 1 , wherein the polyA sequence comprises the nucleotide sequence as set forth in SEQ ID NO:10.
14. The rAAV according to claim 2 , wherein the vector genome is 5.1 kilobases in size.
15. The aqueous suspension according to claim 7 , wherein the vector genome is 5 to 5.5 kilobases in size.
16. The aqueous suspension according to claim 7 , wherein the AAV capsid is an hu37 capsid.
17. The aqueous suspension according to claim 7 , wherein the effective amount of the rAAV is about 1×10 12 GC/kg to about 1×10 14 GC/kg body weight of the patient.