IP Library Granted Patent US 11,680,265
Granted Patent B2
US 11,680,265 · App. 16/858,512 · Granted Jun 20, 2023

Genome editing using effector oligonucleotides for therapeutic treatment

Inventor: Kambiz Shekdar (New York, NY)
Assignee: Research Foundation to Cure AIDS, Inc.
C12N15/1138C12N15/102C12Q1/6876C12N2310/152C12N2310/3181C12N2310/3231C12N2310/333C12N2310/336C12N2310/533C12N2330/50
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Quick Facts
Patent No.
US 11,680,265
App. No.
16/858,512
Granted
Jun 20, 2023
Kind
B2
Abstract

The invention provides compositions and methods of making and using effector oligonucleotides, including effector oligonucleotides with greater than one mismatch as compared to its target sequence. These effector oligonucleotides are useful for improving the efficiency of genomic editing as well as providing therapeutic benefits to individuals in need thereof.

Claims (13)

1. An effector oligonucleotide comprising a sequence selected from the group consisting of SEQ ID NO:5, SEQ ID NO:7, SEQ ID NO:9, and SEQ ID NO:11.

2. The effector oligonucleotide of claim 1 , wherein the effector oligonucleotide comprises a mismatch in a human CCR5 sequence corresponding to a delta-32 CCR5 variant, wherein the effector oligonucleotide matches 40 to 200 bases of the human CCR5 sequence before the mismatch and matches 40 to 200 bases of the human CCR5 sequence after the mismatch.

3. The effector oligonucleotide of claim 1 , wherein the effector oligonucleotide is a modified oligonucleotide.

4. The effector oligonucleotide of claim 3 , wherein the effector oligonucleotide is modified to increase the strength of binding of the oligonucleotide to a target sequence or increase the stability of the oligonucleotide to degradation in buffers and in cells.

5. The effector oligonucleotide of claim 3 , wherein modified oligonucleotide is a peptide nucleic acid (PNA) or comprises one or more bridged nucleotides (BNA).

6. A composition comprising the effector oligonucleotide of claim 1 and a pharmaceutically acceptable carrier.

7. A kit comprising an effector oligonucleotide according to claim 1 .

8. The kit of claim 7 further comprising triplex-forming oligonucleotides or pseudocomplementary oligonucleotides.

9. The kit of claim 8 comprising triplex-forming oligonucleotides, wherein the triplex-forming oligonucleotides comprise a peptide nucleic acid (PNA).

10. The kit of claim 8 further comprising components for the detection of cells treated with the composition that comprise sequence encoded by the effector oligonucleotide.

11. The kit of claim 10 , wherein the components for detection of cells comprise at least one molecular beacon probe.

12. The kit of claim 7 , further comprising instructions for treating HIV infection.

13. The kit of claim 8 , further comprising instructions for treating HIV infection.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE THE ASSIGNEE PREVIOUSLY RECORDED SHOULD BE UPDATED TO RESEARCH FOUNDATION TO CURE AIDS, INC. PREVIOUSLY RECORDED AT REEL: 060842 FRAME: 0078. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jul 19, 2023
From: SHEKDAR, KAMBIZ
To: RESEARCH FOUNDATION TO CURE AIDS, INC.
Reel/Frame 064385/0679 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 18, 2022
From: SHEKDAR, KAMBIZ
To: RESEARCH FOUNDATION TO CURE AIDS
Reel/Frame 060842/0078 →
Continuity (4)
Division 14777490
Provisional Application 61867522 · Aug 19, 2013
Provisional Application 61801822 · Mar 15, 2013
Related Publication 20200407727A1 · Dec 31, 2020