IP Library Granted Patent US 11,571,463
Granted Patent B2
US 11,571,463 · App. 17/721,583 · Granted Feb 7, 2023

Polynucleotides encoding interleukin-12 (IL12) and uses thereof

Inventors: Joshua Frederick (Charlestown, MA); Susannah Hewitt (Jamaica Plain, MA); Ailin Bai (Newton, MA); Stephen Hoge (Brookline, MA); Vladimir Presnyak (Manchester, NH); Iain James McFadyen (Arlington, MA); Kerry Benenato (Sudbury, MA); Ellalahewage Sathyajith Kumarasinghe (Harvard, MA)
Assignee: ModernaTX, Inc.
A61K38/208A61K9/0019A61K9/5123A61K31/7088A61K31/7115A61K48/005A61K48/0008A61K48/0025A61P35/00C07K14/5434C12N15/62A61K48/00
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Quick Facts
Patent No.
US 11,571,463
App. No.
17/721,583
Granted
Feb 7, 2023
Kind
B2
Abstract

The present disclosure relates to polynucleotides comprising an open reading frame of linked nucleosides encoding human interleukin-12 (IL12), functional fragments thereof, and fusion proteins comprising IL12. In some embodiments, the open reading frame is sequence-optimized. In particular embodiments, the disclosure provides sequence-optimized polynucleotides comprising nucleotides encoding the polypeptide sequence of human IL12, or sequences having high sequence identity with those sequence optimized polynucleotides.

Claims (35)

1. A method for reducing the size of a tumor or inhibiting growth of a tumor in a subject who has received or is receiving an immune checkpoint inhibitor which is an antibody, the method comprising administering to the subject a lipid nanoparticle (LNP) encapsulated messenger RNA (mRNA) comprising an open reading frame (ORF) encoding a fusion protein comprising a human IL-12B polypeptide fused directly or by a linker to a human IL-12A polypeptide, wherein the IL-12B polypeptide comprises the amino acid sequence of SEQ ID NO: 1, wherein the IL-12A polypeptide comprises the amino acid sequence of SEQ ID NO: 3, and wherein the LNP comprises an ionizable amino lipid; a phospholipid; a sterol; and a PEG-modified lipid, thereby reducing the size of the tumor or inhibiting growth of the tumor in the subject.

2. The method of claim 1 , wherein the ORF comprises from 5′ to 3′ a nucleotide sequence selected from the group consisting of:

(i) a nucleotide sequence encoding the IL-12B polypeptide, a nucleotide sequence encoding a peptide linker, and a nucleotide sequence encoding the IL-12A polypeptide;

(ii) a nucleotide sequence encoding the IL-12B polypeptide, and a nucleotide sequence encoding the IL-12A polypeptide;

(iii) a nucleotide sequence encoding the IL-12A polypeptide, a nucleotide sequence encoding a peptide linker, and a nucleotide sequence encoding the IL-12B polypeptide; and

(iv) a nucleotide sequence encoding the IL-12A polypeptide, and a nucleotide sequence encoding the IL-12B polypeptide.

3. The method of claim 2 , wherein the ORF comprises a nucleotide sequence encoding a signal peptide located at the 5′ terminus of the ORF.

4. The method of claim 3 , wherein the signal peptide is a human IL-12B signal peptide.

5. The method of claim 1 , wherein the fusion protein comprises the amino acid sequence of SEQ ID NO: 48.

6. The method of claim 1 , wherein the antibody is an anti-PD1 antibody, and anti-PDL1 antibody, or an anti-CTLA4 antibody.

7. A method for reducing the size of a tumor or inhibiting growth of a tumor in a subject who has received or is receiving a LNP encapsulated mRNA comprising an ORF encoding a fusion protein comprising a human IL-12B polypeptide fused directly or by a linker to a human IL-12A polypeptide, wherein the IL-12B polypeptide comprises the amino acid sequence of SEQ ID NO: 1, wherein the IL-12A polypeptide comprises the amino acid sequence of SEQ ID NO: 3, wherein the LNP comprises an ionizable amino lipid; a phospholipid; a sterol; and a PEG-modified lipid, the method comprising administering to the subject an immune checkpoint inhibitor, wherein the immune checkpoint inhibitor is an antibody, thereby reducing the size of the tumor or inhibiting growth of the tumor in the subject.

8. The method of claim 7 , wherein the ORF comprises from 5′ to 3′ a nucleotide sequence selected from the group consisting of:

(i) a nucleotide sequence encoding the IL-12B polypeptide, a nucleotide sequence encoding a peptide linker, and a nucleotide sequence encoding the IL-12A polypeptide;

(ii) a nucleotide sequence encoding the IL-12B polypeptide, and a nucleotide sequence encoding the IL-12A polypeptide;

(iii) a nucleotide sequence encoding the IL-12A polypeptide, a nucleotide sequence encoding a peptide linker, and a nucleotide sequence encoding the IL-12B polypeptide; and

(iv) a nucleotide sequence encoding the IL-12A polypeptide, and a nucleotide sequence encoding the IL-12B polypeptide.

9. The method of claim 8 , wherein the ORF comprises a nucleotide sequence encoding a signal peptide located at the 5′ terminus of the ORF.

10. The method of claim 9 , wherein the signal peptide is a human IL-12B signal peptide.

11. The method of claim 7 , wherein the fusion protein comprises the amino acid sequence of SEQ ID NO: 48.

12. The method of claim 7 , wherein the antibody is an anti-PD1 antibody, and anti-PDL1 antibody, or an anti-CTLA4 antibody.

13. A method for reducing the size of a tumor or inhibiting growth of a tumor in a subject, comprising administering to the subject (i) an immune checkpoint inhibitor, wherein the immune checkpoint inhibitor is an antibody; and (ii) an LNP encapsulated mRNA comprising an ORF encoding a fusion protein comprising a human IL-12B polypeptide fused directly or by a linker to a human IL-12A polypeptide, wherein the IL-12B polypeptide comprises the amino acid sequence of SEQ ID NO: 1, wherein the IL-12A polypeptide comprises the amino acid sequence of SEQ ID NO: 3, wherein the LNP comprises an ionizable amino lipid; a phospholipid; a sterol; and a PEG-modified lipid, thereby reducing the size of the tumor or inhibiting growth of the tumor in the subject.

14. The method of claim 13 , wherein the immune checkpoint inhibitor and the LNP encapsulated mRNA are administered sequentially.

15. The method of claim 13 , wherein the LNP encapsulated mRNA is administered prior to administration of the immune checkpoint inhibitor.

16. The method of claim 13 , wherein the immune checkpoint inhibitor and the LNP encapsulated mRNA are administered concurrently.

17. The method of claim 13 , wherein the ORF comprises from 5′ to 3′ a nucleotide sequence selected from the group consisting of:

(i) a nucleotide sequence encoding the IL-12B polypeptide, a nucleotide sequence encoding a peptide linker, and a nucleotide sequence encoding the IL-12A polypeptide;

(ii) a nucleotide sequence encoding the IL-12B polypeptide, and a nucleotide sequence encoding the IL-12A polypeptide;

(iii) a nucleotide sequence encoding the IL-12A polypeptide, a nucleotide sequence encoding a peptide linker, and a nucleotide sequence encoding the IL-12B polypeptide; and

(iv) a nucleotide sequence encoding the IL-12A polypeptide, and a nucleotide sequence encoding the IL-12B polypeptide.

18. The method of claim 17 , wherein the ORF comprises a nucleotide sequence encoding a human IL-12B signal peptide located at the 5′ terminus of the ORF.

19. The method of claim 13 , wherein the fusion protein comprises the amino acid sequence of SEQ ID NO: 48.

20. The method of claim 13 , wherein the antibody is an anti-PD1 antibody, and anti-PDL1 antibody, or an anti-CTLA4 antibody.

21. The method of claim 1 , wherein the antibody is an anti-PDL1 antibody.

22. The method of claim 7 , wherein the antibody is an anti-PDL1 antibody.

23. The method of claim 13 , wherein the antibody is an anti-PDL1 antibody.

Assignments (2)
SECURITY INTEREST Recorded Nov 19, 2025
From: MODERNATX, INC.
To: ARES CAPITAL CORPORATION, AS AGENT
Reel/Frame 073634/0354 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 15, 2022
From: FREDERICK, JOSHUA; HEWITT, SUSANNAH; BAI, AILIN; HOGE, STEPHEN; PRESNYAK, VLADIMIR; MCFADYEN, IAIN; BENENATO, KERRY; KUMARASINGHE, ELLALAHEWAGE SATHYAJITH
To: MODERNATX, INC.
Reel/Frame 059613/0343 →