IP Library Granted Patent US 9,844,592
Granted Patent B2
US 9,844,592 · App. 14/233,631 · Granted Dec 19, 2017

Bacterial RNAs as vaccine adjuvants

Inventors: Julie Magarian Blander (North Haven, CT); Leif Erik Sander (Berlin, DE)
Assignee: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
A61K39/39A61K39/0011A61K2039/522A61K2039/585
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Quick Facts
Patent No.
US 9,844,592
App. No.
14/233,631
Granted
Dec 19, 2017
Kind
B2
Abstract

The disclosure features vaccine adjuvants comprising prokaryotic mRNA, and methods of vaccination using the adjuvants. More specifically, the disclosure provides a vaccine composition comprising a nonviable immunogen (e.g., heat-killed bacterium), a tumor antigen, or an immunogenic peptide of microbial or mammalian origin, and an adjuvant, wherein adjuvant comprises prokaryotic mRNA (e.g., bacterial mRNA), as well as the methods of using the vaccine compositions. Further disclosed are the structural features of the prokaryotic mRNA used as the adjuvants.

Claims (9)

1. A vaccine composition comprising a nonviable immunogen and an adjuvant, wherein said adjuvant comprises at least one of an mRNA of prokaryotic origin and an RNA of prokaryotic origin, wherein the RNA has structural features comprising a 3′ stem-loop structure, at least one of intramolecular base-pairing and nucleotide modifications, no 5′ cap, no 5′ tri-phosphate group and no 3′ poly(A) tail, and wherein the immunogen is an extracellular pathogen.

2. A vaccine composition comprising a nonviable immunogen and an adjuvant, wherein said adjuvant comprises at least one of an mRNA of prokaryotic origin and an RNA of prokaryotic origin, wherein the RNA has structural features comprising a 3′ stem-loop structure, at least one of intramolecular base-pairing and nucleotide modifications, no 5′ cap, no 5′ tri-phosphate group and no 3′ poly(A) tail, and wherein the immunogen is an intracellular pathogen selected from the group consisting of bacteria, fungi and parasites.

3. A vaccine composition comprising a nonviable immunogen and an adjuvant, wherein said adjuvant comprises at least one of an mRNA of prokaryotic origin and an RNA of prokaryotic origin, wherein the RNA has structural features comprising a 3′ stem-loop structure, at least one of intramolecular base-pairing and nucleotide modifications, no 5′ cap, no 5′ tri-phosphate group and no 3′ poly(A) tail, and wherein the immunogen is a bacterium.

4. The composition of claim 3 , wherein the bacterium is of a genus selected from a group consisting of Escherichia, Streptococcus, Staphylococcus, Clostridium, Campylobacter, Enterococcus, Helicobacter, Moraxella, Acinetobacter, Shigella, Salmonella, Listeria, Legionella, Klebsiella, Pseudomonas, Brucella, Haemophilus, Bordetella, Borrelia, Bacteroides, Bacillus, Chlamydia, Neisseria, Francisella, Yersinia, Vibrio, Mycobacterium, Mycoplasma, Corynebacterium , and Rickettsia.

5. A method of eliciting an immune response in a subject, comprising administering to the subject the composition of any one of claims 1 - 3 .

6. A method of increasing the immune response to a killed vaccine in a subject, comprising administering the killed vaccine to the subject with an adjuvant comprising at least one of an mRNA of prokaryotic origin and an RNA of prokaryotic origin, wherein the RNA has structural features comprising a 3′ stem-loop structure, at least one of intramolecular base-pairing and nucleotide modifications, no 5′ cap, no 5′ tri-phosphate group and no 3′ poly(A) tail.

7. A method of inducing IFN-β or IL-1β production in immune cells, comprising contacting the cells with the composition of any one of claims 1 - 3 .

8. A method of preparing a vaccine composition of any one of claims 1 - 3 , comprising mixing a nonviable immunogen, selected from the group consisting of an extracellular pathogen and an intracellular pathogen, the pathogen being selected from the group consisting of bacteria, fungi and parasites, with at least one of an mRNA of prokaryotic origin and an RNA of prokaryotic origin wherein the RNA has structural features comprising a 3′ stem-loop structure, at least one of intramolecular base-pairing and nucleotide modifications, no 5′ cap, no 5′ tri-phosphate group and no 3′ poly(A) tail.

9. An immunization kit, comprising a vaccine composition comprising a nonviable immunogen, selected from the group consisting of an extracellular pathogen and an intracellular pathogen, the pathogen being selected from the group consisting of bacteria, fungi and parasites, and an adjuvant composition comprising at least one of an mRNA of prokaryotic origin and an RNA of prokaryotic origin, wherein the RNA has structural features comprising a 3′ stem-loop structure, at least one of intramolecular base-pairing and nucleotide modifications, no 5′ cap, no 5′ tri-phosphate group and no 3′ poly(A) tail.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 8, 2020
From: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
To: CORNELL UNIVERSITY
Reel/Frame 051453/0981 →
CONFIRMATORY LICENSE Recorded Feb 12, 2018
From: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 045307/0353 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 25, 2014
From: BLANDER, JULIE M.; SANDER, LEIF ERIK
To: MOUNT SINAI SCHOOL OF MEDICINE
Reel/Frame 032289/0246 →
CHANGE OF NAME Recorded Feb 25, 2014
From: MOUNT SINAI SCHOOL OF MEDICINE
To: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
Reel/Frame 032332/0406 →
Continuity (3)
Provisional Application 61509028 · Jul 18, 2011
Provisional Application 61565733 · Dec 1, 2011
Related Publication 20140186398A1 · Jul 3, 2014