HUMAN RESPIRATORY SYNCYTIAL VIRUS (RSV) VACCINE

التفاصيل البيبلوغرافية
العنوان: HUMAN RESPIRATORY SYNCYTIAL VIRUS (RSV) VACCINE
Document Number: 20110014220
تاريخ النشر: January 20, 2011
Appl. No: 12/505998
Application Filed: July 20, 2009
مستخلص: The present invention relates to a vaccine composition against the infection of human respiratory syncytial virus (RSV) comprising a replication-defective recombinant adenovirus carrying a nucleotide sequence encoding the F protein of RSV or fragment thereof. A method of preventing RSV infection-related diseases using the vaccine composition of the present invention is also provided.
Inventors: Chow, Yen-Hung (Zhunan Town, TW); Shao, Hsiao-Yun (Zhunan Town, TW); Sia, Charles (Zhunan Town, TW); Chong, Pele (Zhunan Town, TW)
Assignees: National Health Research Institutes (Zhunan Town, TW)
Claim: 1. A vaccine composition for the prophylaxis of RSV infection or respiratory syncytial virus (RSV) infection-related diseases comprising an effective amount of a replication-defective recombinant adenoviral construct carrying a nucleotide sequence encoding F protein of RSV or fragments thereof.
Claim: 2. The vaccine composition of claim 1, wherein the RSV is human RSV.
Claim: 3. The vaccine composition of claim 2, wherein the nucleotide sequence encodes the full length of F protein of human RSV.
Claim: 4. The vaccine composition of claim 1, wherein the nucleotide sequence encodes F protein of RSV having the amino acid sequence of SEQ ID NO: 2.
Claim: 5. The vaccine composition of claim 1, wherein the nucleotide sequence encoding F protein of RSV has the nucleotide sequence of SEQ ID NO: 1.
Claim: 6. The vaccine composition of claim 1, wherein the nucleotide sequence encodes a fragment of F protein of RSV is transmembrane coding region-truncated F protein.
Claim: 7. The vaccine composition of claim 5, wherein the nucleotide sequence encodes a fragment of F protein of RSV having the amino acid sequence of SEQ ID NO: 4.
Claim: 8. The vaccine composition of claim 5, wherein nucleotide sequence encoding a fragment of F protein of RSV has the nucleotide sequence of SEQ ID NO: 3.
Claim: 9. The vaccine composition of claim 1, wherein the replication-defective adenovirus is a serotype 5 adenovirus (Ad5).
Claim: 10. The vaccine composition of claim 9, wherein the recombinant adenoviral construct is derived from a replication-defective adenovirus with deletions in its E1 and E3 genes.
Claim: 11. The vaccine composition of claim 1, wherein the RSV infection-related disease is selected from the group consisting of otitis media, bronchilitis, eosinophilia and pneumonia.
Claim: 12. The vaccine composition of claim 1, which is administered transmucosally.
Claim: 13. The vaccine composition of claim 11, which is administered intranasally.
Claim: 14. A method of preventing RSV infection or RSV infection-related diseases comprising administering to a subject in need thereof a vaccine composition comprising an effective amount of a replication-defective recombinant adenoviral construct carrying a nucleotide sequence encoding a polypeptide of F protein of RSV or fragments thereof.
Claim: 15. The method of claim 14, wherein the RSV is human RSV.
Claim: 16. The method of claim 15, wherein the nucleotide sequence encodes the full length of F protein of human RSV.
Claim: 17. The method of claim 14, wherein the nucleotide sequence encodes F protein of RSV having the amino acid sequence of SEQ ID NO: 2.
Claim: 18. The method of claim 14, wherein the nucleotide sequence encoding F protein of RSV has the nucleotide sequence of SEQ ID NO: 1.
Claim: 19. The method of claim 14, wherein the nucleotide sequence encodes a fragment of F protein of RSV is transmembrane coding region-truncated F protein.
Claim: 20. The method of claim 19, wherein the nucleotide sequence encodes a fragment of F protein of RSV having the amino acid sequence of SEQ ID NO: 4.
Claim: 21. The method of claim 19, wherein nucleotide sequence encoding a fragment of F protein of RSV has the nucleotide sequence of SEQ ID NO: 3.
Claim: 22. The method of claim 14, wherein the replication-defective adenovirus is a serotype 5 adenovirus (Ad5).
Claim: 23. The method of claim 22, wherein the recombinant adenoviral construct is derived from a replication-defective adenovirus with deletions in its E1 and E3 genes.
Claim: 24. The method of claim 14, wherein the RSV infection-related disease is selected from the group consisting of otitis media, bronchilitis, eosinophilia and pneumonia.
Claim: 25. The method of claim 14, wherein the vaccine composition is administered transmucosally.
Claim: 26. The method of claim 11, wherein the vaccine composition is administered intranasally.
Current U.S. Class: 4241/861
Current International Class: 61; 61
رقم الانضمام: edspap.20110014220
قاعدة البيانات: USPTO Patent Applications