IP Library Granted Patent US 11,612,619
Granted Patent B2
US 11,612,619 · App. 16/672,185 · Granted Mar 28, 2023

Compostions and methods for enabling cholesterol catabolism in human cells

Inventors: Richard Eric Honkanen (Mobile, AL); Brandon Marshall D'Arcy (Mobile, AL); Mark Raymond Swingle (Mobile, AL)
Assignee: National Institute of Health (NIH), U.S. Dept. of Health and Human Services (DHHS), U.S. Government
A61K35/17C12N5/0636C12N15/52C12N15/62C07K2319/43C12N9/001C12N9/0006C12N9/0077C12N9/0095C12N2710/16141C12N2820/005C12N2820/60C12Y101/01051C12Y101/01145C12Y103/01021C12Y103/99004C12Y106/02004C12Y114/15C12Y114/15006C12Y118/01002
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Quick Facts
Patent No.
US 11,612,619
App. No.
16/672,185
Granted
Mar 28, 2023
Kind
B2
Abstract

Compositions, methods, and systems for modifying sterol metabolism in a subject is disclosed. In some embodiments, the subjects may be administered one or more mammalian cells modified to express at least one sterol degrading enzyme derived from a bacterium. In many embodiments, the cell is a macrophage or monocyte stably expressing three or more enzymes that aid in opening the β ring of cholesterol. The disclosed compositions and methods may be useful in lowering cholesterol levels in a subject in need thereof. In some embodiments, the subject may have a genetic predisposition to atherosclerosis.

Claims (25)

1. A nucleic acid composition comprising:

a coding sequence, coding for one or more proteins selected from humanized forms of cholesterol dehydrogenase (coded for by nucleotides 166 to 1284 of SEQ ID NO:10; CholD), 3-ketosteroid Δ1-dehydrogenase (coded for by nucleotides 170 to 1704 of SEQ ID NO:13; Δ1-KstD), anoxic cholesterol metabolism B enzyme (coded for by nucleotides 74 to 1756 of SEQ ID NO:11; acmB), 3-ketosteroid 9α-hydroxylase (coded for by nucleotides 132 to 1316 and 1416 to 2483 of SEQ ID NO:17; KshAB), 3β-hydroxysteroid dehydrogenase 2 (coded for by nucleotides 3554 to 4672 of SEQ ID NO:12; HSD2), and a fusion protein of P450-ferredoxin reductase-ferredoxin fusion (SEQ ID NO:5; P450-FdxR-Fdx); and

a control sequence, for regulating the transcription of one or more of the coding sequences in a eukaryotic cell.

2. The nucleic acid composition of claim 1 , wherein the one or more proteins are selected from humanized forms of Δ1-KstD, KshAB, HSD2, and P450-FdxR-Fdx.

3. The nucleic acid composition of claim 2 , comprising coding sequences for humanized proteins Δ1-KstD, KshAB, HSD2, and P450-FdxR-Fdx, and wherein the control sequence is a eukaryotic transcription promoter sequence.

4. The nucleic acid composition of claim 3 , wherein the coding sequence comprises nucleotides 1007 to 9817 of the sequence SEQ ID NO: 27, and the eukaryotic transcription promoter sequence is a CMV promoter sequence.

5. A method of regulating a sterol concentration in a subject in need thereof, the method comprising the steps of:

modifying an immune cell of the subject by introducing the nucleic acid composition of claim 1 ;

allowing the immune cell to express one or more sequences from the nucleic acid, wherein the nucleic acid codes for one or more proteins involved in sterol metabolism;

administering the modified cell to the subject, and

allowing the modified cell to degrade the sterol.

6. The method of claim 5 , wherein the protein is selected from Δ1-KstD, KshAB, HSD2, and P450-FdxR-Fdx.

7. The method of claim 6 , wherein the sequences code for humanized proteins Δ1-KstD, KshAB, HSD2, and (P450-FdxR-Fdx) and wherein expression is controlled by a eukaryotic promoter sequence.

8. The method of claim 7 , wherein humanized KshAB is targeted to a mitochondrion of the cell by including a mitochondrial targeting sequence in the KshAB coding sequence.

9. The method of claim 7 , wherein the nucleic acid comprises nucleotides 1007 to 9817 of sequence SEQ ID NO: 27, and the eukaryotic transcription promoter sequence is a CMV promoter sequence.

10. The method of claim 9 , wherein the immune cell is a monocyte or macrophage.

11. A method of altering a eukaryotic cell that cannot catabolize a sterol comprising:

introducing an expression vector comprising the nucleic acid composition of claim 1 into the cell; and

expressing one or more enzymes that catabolize the sterol from the vector.

12. The method of claim 11 , wherein the sterol is cholesterol and the one or more enzymes are selected from Δ1-KstD, acmB, KshAB, HSD2, and P450-FdxR-Fdx.

13. The method of claim 12 , wherein the enzymes are Δ1-KstD, KshAB, HSD2, and P450-FdxR-Fdx.

14. The method of claim 13 , wherein humanized KshAB is targeted to a mitochondrion of the cell by including a mitochondrial targeting sequence in the KshAB coding sequence.

15. The method of claim 14 , wherein the eukaryotic cell is an immune cell.

16. The method of claim 11 , wherein the nucleic acid comprises at least one sequence selected from SEQ ID NOS: 10-27.

17. The method of claim 14 , wherein the nucleic acid comprises nucleotides 1007 to 9817 of sequence SEQ ID NO: 27, and the eukaryotic transcription promoter sequence is a CMV promoter sequence.

Assignments (2)
CONFIRMATORY LICENSE Recorded Sep 26, 2022
From: UNIVERSITY OF SOUTH ALABAMA
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 061536/0129 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 2, 2020
From: HONKANEN, RICHARD ERIC; D'ARCY, BRANDON MARSHALL; SWINGLE, MARK RAYMOND
To: UNIVERSITY OF SOUTH ALABAMA FOUNDATION FOR RESEARCH AND COMMERCIALIZATION
Reel/Frame 051980/0161 →
Continuity (2)
Provisional Application 62754499 · Nov 1, 2018
Related Publication 20200179452A1 · Jun 11, 2020
Cited By (2)
US 12,544,402 US 12,545,918