Base editing approaches for the treatment of betahemoglobinopathies

Patent metadata

Field	Value
Publication number	US-2023279438-A1
Application number	US-202117998603-A
Country	US
Kind code	A1
Filing date	May 12, 2021
Priority date	May 13, 2020
Publication date	Sep 7, 2023
Grant date	—

Abstract

The clinical history of β-hemoglobinopathies shows that the severity is mitigated by the synthesis of the fetal γ-globin in adulthood, typically associated with genetic variants the HBB cluster known as hereditary persistence of fetal hemoglobin (HPFH) mutations. The inventors identified that most of the known HPFH mutations in the γ-globin promoters (C>T, G>A, T>C or A>G) can be recapitulated using CBE- and ABE-mediatedbase-editing approaches. In particular, the inventors designed gRNAs that, when combined with CBEs or ABEs, generate HPFH mutations, and either disrupt binding sites for transcriptional repressors (-200 and -115 sites) or generate de novo DNA motifs recognized by transcriptional activators (e.g., -198 T>C, the -175 T>C and -113 A>G). It is noteworthy that a subset of the gRNAs targeting the -200 and the 115 regions are predicted to generate simultaneously HPFH mutations and also to make base changes other than HPFH mutations in or around the LRF and BCL11A binding sites, which might further reduce LRF and BCL11A occupancy. Accordingly, the present invention relates to base editing approaches for the treatment of β-hemoglobinopathies.

First claim

1 . A method for increasing fetal hemoglobin content in a eukaryotic cell comprising contacting the eukaryotic cell with a gene editing platform comprising (a) at least one base-editing enzyme and (b) at least one guide RNA molecule for guiding the base-editing enzyme to at least one target sequence in the an HBG1 or HBG2 promoter, thereby editing said promoter and subsequently increasing the expression of gamma globin in said eukaryotic cell.

2 . The method of claim 1 wherein the gene editing platform introduces the a -198T>C mutation in the HBG1 or HBG2 promoter so that the KFL1 activator binds to the HBG1 or HBG2 promoter.

3 . The method of claim 1 wherein the gene editing platform introduces the a -175T>C mutation in the HBG1 or HBG2 promoter so that the TAL1 activator binds to the HBG1 or HBG2 promoter.

4 . The method of claim 1 wherein the gene editing platform introduces a -113A>G mutation in the HBG1 or HBG2 promoter thereby permitting binding of a GATA1 activator to the HBG1 or HBG2 promoter.

5 . The method of claim 1 wherein the gene editing platform edits a -200 region in the HBG1 or HBG2 promoter thereby disrupting a binding site for the LRF repressor.

6 . The method of claim 5 wherein the gene editing platform introduces at least one mutation selected from the group consisting of -201C>T, -200C>T, -197C>T, -196C>T, -195C>T and -194C>T in the HBG1 or HBG2 promoter thereby disrupting a binding site for the LRF repressor.

7 . The method of claim 1 wherein the gene editing edits a -115 region in the HBG1 or HBG2 promoter thereby disrupting a binding site for the BCL11A repressor.

8 . The method of claim 7 wherein the gene editing platform introduces at least one mutation selected from the group consisting of -114C>T, -113C>T, -115C>T and -116C>T in the HBG1 or HBG2 promoter thereby disrupting a binding site for the BCL11A repressor.

9 . The method of claim 1 wherein the eukaryotic cell is selected from the group consisting of hematopoietic progenitor cells, hematopoietic stem cells (HSCs), pluripotent cells and induced pluripotent stem cells (iPS)).

10 . The method of claim 1 wherein the at least one base-editing enzyme comprises a nickase.

11 . The method of claim 10 wherein the nickase comprises the amino acid sequence as set forth in SEQ ID NO: 3 or SEQ ID NO:33.

12 . The method of claim 1 wherein the at least one base-editing enzyme is a cytidine deaminase or an adenosine deaminase.

13 . The method of claim 12 wherein the cytidine deaminase or the adenosine deaminase comprises a variant of the amino acid sequence as set forth in SEQ ID NO:4-14.

14 . The method of claim 1 wherein the at least one base-editing enzyme is ABEmax, AncBE4max, or evoCDA1-BE4max-NG.

15 . The method of claim 1 wherein the at least one base-editing enzyme and the at least one guide RNA molecule is chosen according to Table B.

16 . The method of claim 1 wherein a plurality of guide RNA molecules are designed for targeting a plurality of sequences in the HBG1 or HBG2 promoter.

17 . The method of claim 1 wherein a plurality of base-editing enzymes and a plurality of guide RNA molecules are designed for targeting a plurality of sequences in the HBG1 or HBG2 promoter.

18 . A method for increasing fetal hemoglobin levels in a subject in need thereof, comprising transplanting into the subject a therapeutically effective amount of a population of eukaryotic cells obtained by the method of claim 1 .

19 . The method of claim 18 wherein the subject has been diagnosed with a hemoglobinopathy.

20 . The method of claim 9 , wherein the pluripotent cells are embryonic stem (ES) cells.

21 . The method of claim 10 , wherein the nickase is a Cas9 nickase.

22 . The method of claim 19 wherein the hemoglobinopathy is sickle cell disease or β-thalassemia.

Assignees

• Inserm Institut National De La Sante Et La Rech Medicale
• Univ Paris Cite
• Hopitaux Paris Assist Publique
• Fond Imagine

Inventors

• Miccio Annarita
• Antoniou Panagiotis
• Cavazzana Marina

Classifications

• C12N15/90 Primary

  Stable introduction of foreign DNA into chromosome · CPC title

• C12N9/22

  Ribonucleases {[RNase]; Deoxyribonucleases [DNase]} · CPC title

• C12N9/78

  acting on carbon to nitrogen bonds other than peptide bonds (3.5) · CPC title

• C12N15/11

  DNA or RNA fragments; Modified forms thereof (DNA or RNA not used in recombinant technology, C07H21/00); {Non-coding nucleic acids having a biological activity} · CPC title

• C12Y305/04005

  Cytidine deaminase (3.5.4.5) · CPC title