RNAi-mediated inhibition of H1F1A for treatment of ocular angiogenesis
View Patent ↗RNA interference is provided for inhibition of HIF1A mRNA expression for treating patients with ocular angiogenesis, particularly for treating retinal edema, diabetic retinopathy, sequela associated with retinal ischemia, posterior segment neovascularization (PSNV), and neovascular glaucoma, and for treating patients at risk of developing such conditions.
1. A method of attenuating expression of HIF1A mRNA in a subject, the method comprising:
administering to an eye of the subject a composition comprising an effective amount of interfering RNA having a length of 19 to 49 nucleotides and a pharmaceutically acceptable carrier, the interfering RNA comprising:
a region of at least 13 contiguous nucleotides having at least 90% sequence complementarity to, or at least 90% sequence identity with, the penultimate 13 nucleotides of the 3′ end of an mRNA corresponding to SEQ ID NO: 3,
wherein the interfering RNA is administered by ocular tissue injection, and wherein the expression of HIF1A mRNA is thereby attenuated.
2. The method of claim 1 wherein the interfering RNA comprises a region of at least 14 contiguous nucleotides having at least 85% sequence complementarity to, or at least 85% sequence identity with, the penultimate 14 nucleotides of the 3′ end of an mRNA corresponding to the sequence identified by the sequence identifier.
3. The method of claim 1 wherein the interfering RNA comprises a region of at least 15, 16, 17, or 18 contiguous nucleotides having at least 80% sequence complementarity to, or at least 80% sequence identity with, the penultimate 15, 16, 17, or 18 nucleotides, respectively, of the 3′ end of an mRNA corresponding to the sequence identified by the sequence identifier.
4. The method of claim 1 wherein the composition further comprises a second interfering RNA having a length of 19 to 49 nucleotides and comprising a region of at least 13 contiguous nucleotides having at least 90% complementarity to, or at least 90% sequence identity with, the penultimate 13 nucleotides of the 3′ end of a second mRNA corresponding to any one of SEQ ID NO: 3, and SEQ ID NO:9-SEQ ID NO:51.
5. The method of claim 1 wherein the interfering RNA is an shRNA, siRNA, or miRNA.
6. The method of claim 1 wherein the composition is administered via a intravitreal, periocular, conjunctival, subtenon, intracameral, subretinal, subconjunctival, retrobulbar, or intracanalicular route.
7. The method of claim 1 wherein the composition is administered via in vivo expression from an interfering RNA expression vector.
8. A method of treating ocular angiogenesis in a subject in need thereof, the method comprising:
administering to an eye of the subject a composition comprising an effective amount of interfering RNA having a length of 19 to 49 nucleotides and a pharmaceutically acceptable carrier, the interfering RNA comprising:
a region of at least 13 contiguous nucleotides having at least 90% sequence complementarity to, or at least 90% sequence identity with, the penultimate 13 nucleotides of the 3′ end of an mRNA corresponding to SEQ ID NO: 3,
wherein the interfering RNA is administered by ocular tissue injection, and wherein the ocular angiogenesis is treated thereby.
9. The method of claim 8 wherein the subject has retinal edema, retinal ischemia or diabetic retinopathy.
10. The method of claim 8 wherein the interfering RNA is an shRNA, siRNA, or miRNA.
11. The method of claim 8 wherein the composition is administered via a intravitreal, conjunctival, subtenon, intracameral, subretinal, subconjunctival, or intracanalicular route.
12. The method of claim 8 wherein the composition is administered via in vivo expression from an interfering RNA expression vector.