IP Library Granted Patent US 9,623,095
Granted Patent B2
US 9,623,095 · App. 13/824,705 · Granted Apr 18, 2017

Vaccination in newborns and infants

Inventors: Karl-Josef Kallen (Tuebingen, DE); Thomas Kramps (Tuebingen, DE); Margit Schnee (Constance, DE); Benjamin Petsch (Tuebingen, DE); Lothar Stitz (Rottenburg, DE)
Assignee: CureVac AG
A61K39/00A61K39/12A61K39/145A61K45/06A61K47/48192A61K47/48323A61K47/48853A61K2039/53A61K2039/55A61K2039/572C12N2760/16134
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Quick Facts
Patent No.
US 9,623,095
App. No.
13/824,705
Granted
Apr 18, 2017
Kind
B2
Abstract

The present invention relates to vaccines comprising at least one mRNA encoding at least one antigen for use in the treatment of a disease in newborns and/or infants, preferably exhibiting an age of not more than 2 years, preferably of not more than 1 year, more preferably of not more than 9 months or even 6 months, wherein the treatment comprises vaccination of the newborn or infant and eliciting an immune response in said newborn or infant. The present invention is furthermore directed to kits and kits of parts comprising such a vaccine and/or its components and to methods applying such a vaccine or kit.

Claims (15)

1. A method for stimulating an immune response in an infant subject comprising, administering an effective amount of a composition comprising a purified mRNA encoding an influenza hemagglutinin (HA) virus antigen to the infant subject thereby stimulating an antigen-specific Th1 immune response in the subject, said infant subject being no more than 2 years of age, wherein the composition is administered via injection.

2. The method of claim 1 , wherein the mRNA comprises an increased G/C content relative to a wild type RNA encoding the antigen, a cap and/or a polyA tail.

3. The method of claim 1 , wherein the subject is no more than 1 year of age.

4. The method of claim 3 , wherein the subject is no more than 6 months of age.

5. The method of claim 1 , wherein the composition is administered parenterally.

6. The method of claim 1 , wherein the composition is administered intradermally.

7. The method of claim 1 , wherein the composition comprises the mRNA in an aqueous solution.

8. The method of claim 7 , wherein the aqueous solution is a Ringer's lactate solution.

9. The method of claim 1 , wherein at least a portion of the mRNA is complexed with a cationic or polycationic compound.

10. The method of claim 9 , wherein a portion of the mRNA is complexed with the cationic or polycationic compound and a portion of the mRNA is free from complex.

11. The method of claim 9 , wherein the cationic or polycationic compound is a polypeptide.

12. The method of claim 11 , wherein the polypeptide is protamine.

13. The method of claim 1 , wherein at least a portion of the mRNA encoding the antigen is complexed with a polymeric carrier formed by disulphide-crosslinked cationic polypeptides.

14. The method of claim 1 , further comprising administering an adjuvant to the infant subject.

15. The method of claim 14 , wherein the adjuvant is an immunostimulatory RNA (isRNA).

Assignments (3)
CHANGE OF NAME Recorded Jan 5, 2023
From: CUREVAC AG
To: CUREVAC SE
Reel/Frame 062300/0261 →
CHANGE OF NAME Recorded Nov 16, 2015
From: CUREVAC GMBH
To: CUREVAC AG
Reel/Frame 037115/0430 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 10, 2013
From: KALLEN, KARL-JOSEF; KRAMPS, THOMAS; SCHNEE, MARGIT; PETSCH, BENJAMIN; STITZ, LOTHAR
To: CUREVAC GMBH
Reel/Frame 030771/0875 →
Priority Claims (1)
WO PCT/EP2011/001047 · Mar 2, 2011 · international
Continuity (1)
Related Publication 20130336998A1 · Dec 19, 2013