IP Library Granted Patent US 9,889,194
Granted Patent B2
US 9,889,194 · App. 14/375,083 · Granted Feb 13, 2018

Immunogenic composition for MERS coronavirus infection

Inventors: Shibo Jiang (New York, NY); Lanying Du (New York, NY); Yusen Zhou (Beijing, CN); Guangyu Zhao (Beijing, CN)
Assignee: New York Blood Center, Inc.
A61K39/215A61K39/12C07K14/005C07K16/10C12N7/00A61K2039/55561A61K2039/55566A61K2039/575C07K2319/21C07K2319/30C12N2770/20021C12N2770/20022C12N2770/20034
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Quick Facts
Patent No.
US 9,889,194
App. No.
14/375,083
Granted
Feb 13, 2018
Kind
B2
Abstract

Described herein are immunogenic compositions for preventing infection with Middle East respiratory syndrome coronavirus (MERS-CoV) wherein the immunogenic compositions comprise at least a portion of the MERS-CoV S protein and an immunopotentiator.

Claims (27)

1. A protein comprising:

a Middle East respiratory syndrome coronavirus (MERS-CoV) spike (S) protein sequence (SEQ ID NO: 1), or fragment thereof wherein said fragment comprises amino acids 350-588 of the MERS-CoV S protein sequence (SEQ ID NO:4), amino acids 358-588 of the MERS-CoV S protein sequence (SEQ ID NO:5), amino acids 367-588 of the MERS-CoV S protein sequence (SEQ ID NO:6), amino acids 377-588 of the MERS-CoV S protein sequence (SEQ ID NO:3), or amino acids 367-606 of the MERS-CoV S protein sequence (SEQ ID NO:7); and

an immunopotentiator protein sequence, wherein the immunopotentiator sequence comprises an amino acid sequence of an Fc fragment of human IgG (Fc), a C3d protein, an Onchocerca volvulus ASP-1, a cholera toxin, a muramyl peptide, or a cytokine.

2. The protein of claim 1 , wherein said fragment of the MERS-CoV S protein sequence comprises an MERS-CoV S1 protein sequence, a receptor-binding domain (RBD) sequence of an MERS-CoV S protein, a fusion peptide sequence of an MERS-CoV S protein, a heptad repeat sequence of an MERS-CoV S protein, or a transmembrane domain sequence of an MERS-CoV S protein.

3. The protein of claim 2 , the MERS-CoV S1 protein sequence, the RBD sequence of the MERS-CoV S protein, the fusion peptide sequence of the MERS-CoV S protein, the heptad repeat sequence of the MERS-CoV S protein, or the transmembrane domain sequence of the MERS-CoV S protein.

4. The protein of claim 2 , the MERS-CoV S1 protein sequence, the RBD sequence of the MERS-CoV S protein, the fusion peptide sequence of the MERS-CoV S protein, the heptad repeat sequence of the MERS-CoV S protein, or the transmembrane domain sequence of the MERS-CoV S protein.

5. The protein of claim 2 , wherein the MERS-CoV S1 protein sequence, the RBD sequence of the MERS-CoV S protein, the fusion peptide sequence of the MERS-CoV S protein, the heptad repeat sequence of the MERS-CoV S protein, or the transmembrane domain sequence of the MERS-CoV S protein.

6. The protein of claim 1 , wherein the MERS-CoV S protein sequence comprises amino acids 377-588 of the MERS-CoV S protein sequence (SEQ ID NO:3).

7. The protein of claim 1 , wherein the immunopotentiator sequence is a human Fc sequence.

8. The protein of claim 1 , wherein the protein further comprises a stabilization sequence disposed between the MERS-CoV S protein sequence and the immunopotentiator sequence.

9. The protein of claim 8 , wherein the stabilization sequence is a foldon (Fd) or GCN4.

10. The protein of claim 1 , wherein the protein further comprises a linker sequence disposed between the MERS-CoV S protein sequence and the immunopotentiator sequence, and the linker is 1 to 8 tandem copies of (GGGGS) n (SEQ ID NO:24).

11. The protein according to claim 10 , wherein n is 1.

12. The protein of claim 1 , wherein the protein comprises the sequence of S377-588-Fc (SEQ ID NO:12).

13. An immunogenic composition comprising a protein according to claim 1 .

14. A method of inducing a protective immune response against MERS-CoV comprising:

administering the immunogenic composition of claim 13 to a subject in need thereof;

wherein the immunogenic composition induces a protective immune response against challenge with MERS-CoV in the host.

15. The method according to claim 14 , wherein the immunogenic composition further comprises an adjuvant.

16. The method according to claim 14 , wherein the administering step comprises a prime immunization and at least one boost immunization.

17. The method according to claim 16 , wherein the boost immunizations are administered at least twice.

18. The method according to claim 17 , wherein the boost immunizations are administered weekly, every other week, monthly, or every other month.

19. The method according to claim 17 , wherein the boost immunizations are administered weekly, every 2 weeks, every 3 weeks, every 4 weeks, every 5 weeks, every 6 weeks, every 7 weeks, every 8 weeks, every 9 weeks, every 10 weeks, every 11 weeks, or every 12 weeks.

20. The protein of claim 1 , wherein said fragment of the MERS-CoV S protein sequence comprises amino acids 350-588 of the MERS-CoV S protein sequence (SEQ ID NO:4).

21. The protein of claim 1 , wherein said fragment of the MERS-CoV S protein sequence comprises amino acids 358-588 of the MERS-CoV S protein sequence (SEQ ID NO:5).

22. The protein of claim 1 , wherein said fragment of the MERS-CoV S protein sequence comprises amino acids 367-588 of the MERS-CoV S protein sequence (SEQ ID NO:6).

23. The protein of claim 1 , wherein said fragment of the MERS-CoV S protein sequence comprises amino acids 367-606 of the MERS-CoV S protein sequence (SEQ ID NO:7).

Assignments (2)
CONFIRMATORY LICENSE Recorded Jul 26, 2017
From: NEW YORK BLOOD CENTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 043338/0959 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 5, 2015
From: JIANG, SHIBO; DU, LANYING
To: NEW YORK BLOOD CENTER, INC.
Reel/Frame 036262/0022 →
Continuity (3)
Provisional Application 61771561 · Mar 1, 2013
Provisional Application 61941076 · Feb 18, 2014
Related Publication 20160296617A1 · Oct 13, 2016