IP Library Granted Patent US 10,543,269
Granted Patent B2
US 10,543,269 · App. 16/368,099 · Granted Jan 28, 2020

hMPV RNA vaccines

Inventors: Giuseppe Ciaramella (Sudbury, MA); Sunny Himansu (Winchester, MA)
Assignee: ModernaTX, Inc.
A61K39/155A61K39/12C07K16/10C07K16/1027A61K2039/53A61K2039/55511A61K2039/55555A61K2039/6018A61K2039/70C07K2317/76C12N2760/18034C12N2760/18334C12N2760/18434C12N2760/18534C12N2760/18634C12N2770/20034Y02A50/39
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Quick Facts
Patent No.
US 10,543,269
App. No.
16/368,099
Granted
Jan 28, 2020
Kind
B2
Abstract

The disclosure relates to respiratory virus ribonucleic acid (RNA) vaccines and combination vaccines, as well as methods of using the vaccines and compositions comprising the vaccines.

Claims (25)

1. A human metapneumovirus (hMPV) vaccine, comprising: an isolated messenger ribonucleic acid (mRNA) polynucleotide comprising an open reading frame encoding an antigenic hMPV Fusion (F) protein formulated in a lipid nanoparticle that comprises a molar ratio of 20-60% ionizable cationic lipid, 5-25% non-cationic lipid, 25-55% sterol, and 0.5-15% PEG-modified lipid in an effective amount to induce a T cell response and a neutralizing antibody response against hMPV F protein in a subject administered at least one dose of the vaccine, wherein the isolated mRNA polynucleotide is not self-replicating mRNA.

2. A method of inducing an antigen-specific immune response in a subject, the method comprising administering to the subject the vaccine of claim 1 to produce an antigen-specific immune response in the subject.

3. The hMPV vaccine of claim 1 , wherein the isolated mRNA polynucleotide further encodes a 5′ terminal cap, 7mG(5′)ppp(5′)NlmpNp.

4. The hMPV vaccine of claim 1 , wherein at least 80% of the uracil in the open reading frame comprises a chemical modification selected from N1-methyl-pseudouridine and N1-ethyl-pseudouridine.

5. The hMPV vaccine of claim 1 , wherein the chemical modification is in the 5-position of the uracil.

6. The hMPV vaccine of claim 1 , wherein the open reading frame encoding an antigenic hMPV F protein comprises a mRNA sequence that has at least 90% identity to the sequence set forth in SEQ ID NO: 57.

7. The hMPV vaccine of claim 6 , wherein the open reading frame encoding an antigenic hMPV F protein comprises the sequence set forth as SEQ ID NO: 57.

8. The hMPV vaccine of claim 1 , wherein the antigenic hMPV F protein comprises an amino acid sequence that has at least 90% identity to the amino acid sequence set forth as SEQ ID NO: 5.

9. The hMPV vaccine of claim 8 , wherein the antigenic hMPV F protein comprises the amino acid sequence set forth as SEQ ID NO: 5.

10. The hMPV vaccine of claim 1 , wherein the effective amount is a total dose of 25 μg-200 μg.

11. The hMPV vaccine of claim 1 , wherein the isolated mRNA polynucleotide further comprises 5′ terminal cap, a 5′ UTR, a 3′ UTR, and a polyA tail.

12. The hMPV vaccine of claim 11 , wherein the open reading frame encoding an antigenic hMPV F protein comprises an mRNA sequence that has at least 90% identity to the sequence set forth in SEQ ID NO: 57.

13. The hMPV vaccine of claim 12 , wherein the open reading frame encoding an antigenic hMPV F protein comprises the sequence set forth as SEQ ID NO: 57.

14. The hMPV vaccine of claim 1 , wherein the efficacy of the vaccine in vaccinated subjects is at least 60%, relative to unvaccinated subjects, following a single dose of the vaccine.

15. The hMPV vaccine of claim 1 , wherein a single dose of the vaccine administered to a subject is sufficient to produce detectable levels of hMPV F protein as measured in serum of a subject vaccinated with at least one dose of the vaccine at 1-72 hours post administration.

16. The hMPV vaccine of claim 1 , wherein a single dose of the vaccine administered to a subject is sufficient to produce a 1,000-10,000 neutralization titer produced by neutralizing antibody against the antigenic hMPV F protein as measured in serum of a subject vaccinated with at least one dose of the vaccine at 1-72 hours post administration.

17. The hMPV vaccine of claim 16 , wherein the 1,000-10,000 neutralization titer is produced in the absence of antibody-dependent enhancement (ADE) of a hMPV-associated disease.

18. The hMPV vaccine of claim 17 , wherein the hMPV-associated disease is alevolitis interstitial pneumonia.

19. The hMPV vaccine of claim 1 , wherein an anti-hMPV F protein antibody titer produced in a subject vaccinated with at least one dose of the vaccine is increased by at least 1 log relative to a control, wherein the control is an anti-hMPV F protein antibody titer produced in a subject who has not been administered a vaccine against hMPV.

20. The hMPV vaccine of claim 1 , wherein an anti-hMPV F protein antibody titer produced in a subject vaccinated with at least one dose of the vaccine is increased at least 2 times relative to a control, wherein the control is an anti-hMPV F protein antibody titer produced in a subject who has not been administered a vaccine against hMPV.

21. The hMPV vaccine of claim 1 , wherein the ionizable cationic lipid comprises the following compound:

22. The hMPV vaccine of claim 1 , wherein the noncationic lipid is DSPC (1,2-Distearoyl-sn-glycero-3-phosphocholine).

23. The hMPV vaccine of claim 1 , wherein the PEG-modified lipid is DMG-PEG (1,2-dimyristoyl-racglycero-3-methoxypolyethylene glycol-2000).

24. The method of claim 1 , wherein the lipid nanoparticle comprises 40-50% ionizable cationic lipid, 5-15% DSPC, 25-40% cholesterol, and 1-3.5% DMG-PEG.

25. The method of claim 24 , wherein the lipid nanoparticle comprises 50% ionizable cationic lipid, 10% DSPC, 38.5% cholesterol, and 1.5% DMG-PEG.

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 May 10, 2019
From: CIARAMELLA, GIUSEPPE; HIMANSU, SUNNY
To: MODERNATX, INC.
Reel/Frame 049141/0863 →
Cited By (3)
US 12,521,577 US 12,551,734 US 12,629,412