Lassa virus vaccine
The present invention provides mRNAs usable as vaccines against lassa virus (LASV) infections. Further, the Invention relates to (pharmaceutical) compositions and vaccines comprising said mRNAs and their use for treatment or prophylaxis of a lassa virus infection. The present invention further features a kit comprising the mRNAs, (pharmaceutical) compositions or vaccines and a method for treatment or prophylaxis of lassa virus infections using said mRNAs, (pharmaceutical) compositions or vaccines.
1. A purified mRNA molecule comprising: a coding region encoding
a Lassa virus Nucleoprotein (NP), said coding region comprising a RNA sequence at least about 95% identical to one of SEQ ID NOs: 937-1125, 1312-1500, 1687-1875, 2062-2250, 2437-2625, 2812-3000 or 3187-3375,
wherein said mRNA comprises a 5′ cap, a heterologous 3′-UTR element and Poly-A sequence.
2. The purified mRNA molecule of claim 1 , wherein the Lassa virus is from Lassa virus clade I.
3. The purified mRNA molecule of claim 1 , wherein the mRNA comprises a modified nucleotide.
4. The purified mRNA molecule of claim 3 , wherein the modified nucleotide is pseudouridine or 1-methyl-pseudouridine.
5. The purified mRNA molecule of claim 1 , wherein the mRNA comprises at least one histone stem-loop.
6. The purified mRNA molecule of claim 1 , wherein the poly(A) sequence comprises 10 to 200 adenosine nucleotides.
7. The purified mRNA molecule of claim 1 , wherein the mRNA sequence comprises a 5′-UTR element.
8. A composition comprising the purified mRNA of claim 1 and a pharmaceutically acceptable carrier.
9. The composition of claim 8 , wherein the mRNA is complexed with a cationic or polycationic compound.
10. The composition of claim 8 , wherein the mRNA is formulated with lipid nanoparticles.
11. The composition of claim 8 , wherein the composition comprises at least one adjuvant.
12. A method of treatment or prophylaxis of a Lassa virus infection comprising administering the composition of claim 8 to an organism.
13. The method of claim 12 , wherein the administering the composition is by injection of the composition.
14. The method of claim 13 , wherein the injection is an intramuscular injection.