| CPC A61K 39/12 (2013.01) [A61P 31/14 (2018.01); A61P 37/04 (2018.01); A61K 2039/5254 (2013.01); A61K 2039/5256 (2013.01); A61K 2039/54 (2013.01); A61K 2039/545 (2013.01); A61K 2039/70 (2013.01)] | 10 Claims |

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1. A combined vaccine against human respiratory syncytial virus (RSV) infection, comprising: a first composition and a second composition, wherein
the first composition comprises an immunologically effective dosage of a replication-deficient human adenovirus type 26 vector and a pharmaceutically acceptable vector, and the replication-deficient human adenovirus type 26 vector comprises a nucleotide encoding an antigenic protein of RSV;
the second composition comprises an immunologically effective dosage of a replication-deficient chimpanzee adenovirus type 63 vector and a pharmaceutically acceptable vector, and the replication-deficient chimpanzee adenovirus type 63 vector comprises a nucleotide encoding an antigenic protein of RSV; and
the first composition is a primary immunization composition and the second composition is a booster immunization composition; alternatively, the first composition is the booster immunization composition, and the second composition is the primary immunization composition,
wherein in the first composition, the replication-deficient human adenovirus type 26 vector comprises a nucleotide encoding an attachment glycoprotein 130-230aa (G 130-230) of RSV, the nucleotide sequence of which is set forth in SEQ ID NO: 2: or
wherein in the first composition, the replication-deficient human adenovirus type 26 vector comprises a nucleotide encoding both a pre-fusion fusion glycoprotein (preF) and G 130-230 of RSV, the nucleotide sequence of which is set forth in SEQ ID NO: 3.
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