| CPC A61K 39/116 (2013.01) [A61K 39/04 (2013.01); A61K 39/092 (2013.01); A61K 39/095 (2013.01); A61K 39/102 (2013.01); A61K 39/385 (2013.01); A61K 47/6415 (2017.08); A61K 47/646 (2017.08); A61P 31/16 (2018.01); A61P 37/04 (2018.01); A61K 39/145 (2013.01); A61K 2039/5252 (2013.01); A61K 2039/5254 (2013.01); A61K 2039/53 (2013.01); A61K 2039/543 (2013.01); A61K 2039/545 (2013.01); A61K 2039/55555 (2013.01); A61K 2039/55566 (2013.01); A61K 2039/55572 (2013.01); A61K 2039/575 (2013.01); A61K 2039/6037 (2013.01); A61K 2039/6043 (2013.01); A61K 2039/6068 (2013.01); A61K 2039/70 (2013.01)] | 28 Claims |
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1. An immunogenic antigen comprised of:
a contiguous peptide containing one or more bacterial epitopes and one or more influenza epitopes, and
a T cell stimulating epitope and/or an adjuvant,
wherein the one or more bacterial epitopes are selected from the group consisting of cell wall epitopes of Mycobacteria, and the one or more influenza epitopes are selected from the group consisting of epitopes of hemagglutinin (HA), neuraminidase (NA) and matrix proteins of influenza virus, wherein the contiguous peptide comprises the sequences of one or more of SEQ ID NOs. 1-20 and one or more of SEQ ID NOs. 25-28, or the sequence of one or more of SEQ ID NOs. 9-17 and 20-23.
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