IP Library Granted Patent US 10,588,964
Granted Patent B2
US 10,588,964 · App. 15/809,130 · Granted Mar 17, 2020

Bacterial RNAs as vaccine adjuvants

Inventors: Julie Magarian Blander (North Haven, CT); Leif Erik Sander (Berlin, DE)
Assignee: Cornell University
A61K39/39A61K39/0011A61K2039/522A61K2039/585Y02A50/403Y02A50/478
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Quick Facts
Patent No.
US 10,588,964
App. No.
15/809,130
Granted
Mar 17, 2020
Kind
B2
Abstract

The invention features vaccine adjuvants comprising prokaryotic mRNA, and methods of vaccination using the adjuvants.

Claims (18)

1. A vaccine composition comprising a tumor antigen and an adjuvant, wherein said adjuvant comprises prokaryotic mRNA, wherein the prokaryotic mRNA has structural features comprising a 3′ stem loop structure, intramolecular base-pairing, and no 3′ poly(A) tail.

2. The composition of claim 1 , wherein the tumor antigen is carried by a cell.

3. The composition of claim 2 , wherein the prokaryotic mRNA is contained in the cell.

4. A vaccine composition comprising an immunogenic peptide of microbial or mammalian origin and an adjuvant, wherein said adjuvant comprises prokaryotic mRNA, wherein the prokaryotic mRNA has structural features comprising a 3′ stem loop structure, intramolecular base-pairing, and no 3′ poly(A) tail.

5. The composition of claim 4 , wherein the immunogenic peptide is carried by a cell.

6. The composition of claim 5 , wherein the prokaryotic mRNA is contained in the cell.

7. The composition of claim 1 , wherein the mRNA has no 5′ tri-phosphate group.

8. The composition of claim 1 , wherein the mRNA contains nucleotide modifications.

9. A method of eliciting an immune response in a subject, comprising administering to the subject the composition of claim 1 .

10. The method of claim 9 , wherein the subject is human.

11. The method of claim 9 , wherein the immune response protects the subject from developing a cancer, or treats a subject in need of cancer immunotherapy.

12. The method of claim 9 , wherein the immune response comprises one or more of the following: IL-1β production, IFN-β production, increased IgG isotype levels, increased primary and secondary T cell responses, and death of infected cells.

13. A method of inducing IFN-β or IL-1β production in immune cells, comprising contacting the cells with the composition of claim 1 .

14. A method of preparing a vaccine composition of claim 1 , comprising mixing a tumor antigen with prokaryotic mRNA.

15. An immunization kit, comprising a vaccine composition comprising a tumor antigen, and an adjuvant composition comprising prokaryotic mRNA, wherein the prokaryotic mRNA has structural features comprising a 3′ stem loop structure, intramolecular base-pairing, and no 3′ poly(A) tail.

16. The composition of claim 1 , wherein the vaccine further comprises a second adjuvant.

17. The composition of claim 16 , wherein the second adjuvant is lipopolysaccharide.

18. The composition of claim 16 , wherein the second adjuvant is monophosphoryl lipid A.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 8, 2020
From: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
To: CORNELL UNIVERSITY
Reel/Frame 051453/0981 →
CHANGE OF NAME Recorded Nov 10, 2017
From: MOUNT SINAI SCHOOL OF MEDICINE
To: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
Reel/Frame 044748/0228 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 10, 2017
From: BLANDER, JULIE MAGARIAN; SANDER, LEIF ERIK
To: MOUNT SINAI SCHOOL OF MEDICINE
Reel/Frame 044090/0027 →
Continuity (4)
Continuation 14233631
Provisional Application 61565733 · Dec 1, 2011
Provisional Application 61509028 · Jul 18, 2011
Related Publication 20180326050A1 · Nov 15, 2018