| CPC A61K 39/015 (2013.01) [A61K 9/0019 (2013.01); A61K 47/6901 (2017.08); A61P 33/06 (2018.01); A61K 2039/5256 (2013.01); A61K 2039/54 (2013.01)] | 17 Claims |
|
1. A pharmaceutical composition comprising at least one recombinant modified vaccinia Ankara (MVA) viral vector and a pharmaceutically acceptable adjuvant, wherein the recombinant MVA viral vector comprises:
i) a first nucleic acid sequence encoding a Plasmodium falciparum immunogenic polypeptide selected from the group consisting of circumsporozoite protein (CSP) and gametocyte surface protein P230 (Pfs230), the Plasmodium falciparum immunogenic polypeptide further comprising a transmembrane domain of a glycoprotein (GP) of Marburg virus; and
ii) a second nucleic acid sequence encoding a Marburg virus VP40 matrix protein;
wherein the CSP immunogenic polypeptide comprises the amino acid sequence of SEQ ID NO: 2, or an amino acid sequence at least 98% identical thereto;
wherein the Pfs230 immunogenic polypeptide comprises the amino acid sequence of SEQ ID NO: 6, or an amino acid sequence at least 98% identical thereto;
wherein the Marburg virus VP40 matrix protein comprises the amino acid sequence of SEQ ID NO: 8, or an amino acid sequence at least 98% identical thereto;
wherein both the first nucleic acid and the second nucleic acid sequence are under the control of promoters compatible with poxvirus expression systems; and,
wherein upon expression, the Plasmodium falciparum immunogenic polypeptide and Marburg virus VP40 matrix protein are capable of assembling together to form virus like particles (VLPs).
|