US2011070263A1PendingUtilityA1

Influenza hemagglutinin and neuraminidase variants

Assignee: MEDIMMUNE LLCPriority: Mar 8, 2005Filed: Aug 17, 2010Published: Mar 24, 2011
Est. expiryMar 8, 2025(expired)· nominal 20-yr term from priority
C12N 2760/16234A61K 39/145C12N 2760/16222A61K 2039/525C07K 14/11C12N 7/045C12N 2760/16122A61P 37/04A61K 2039/5254C12N 9/2402C12N 2760/16134A61K 39/12A61P 31/16C12Y 302/01018C07K 14/005
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Claims

Abstract

Polypeptides, polynucleotides, methods, compositions, and vaccines comprising influenza hemagglutinin and neuraminidase variants are provided.

Claims

exact text as granted — not AI-modified
1 - 82 . (canceled) 
     
     
         83 . A reassortant influenza virus comprising a polynucleotide selected from the group consisting of:
 a) a polynucleotide comprising the nucleotide sequence of any one of SEQ ID NO:36-48, or a complementary sequence thereof; and   b) a polynucleotide sequence encoding a polypeptide comprising the amino acid sequence of any one of SEQ ID NO:84-96, or a complementary polynucleotide sequence thereof.   
     
     
         84 . The virus of  claim 83 , wherein the virus is a 6:2 reassortant virus, which virus comprises 6 internal genome segments from one or more donor virus and 2 genome segments comprising a polynucleotide comprising the nucleotide sequence of any one of SEQ ID NO:36-48. 
     
     
         85 . The virus of  claim 84 , wherein the donor virus is A/Ann Arbor/6/60, B/Ann Arbor/1/66, A/Puerto Rico/8/34, B/Leningrad/14/17/55, B/14/5/1, B/USSR/60/69, B/Leningrad/179/86, B/Leningrad/14/55, or B/England/2608/76. 
     
     
         86 . An immunogenic composition comprising an immunologically effective amount of the reassortant influenza virus of  claim 84 . 
     
     
         87 . A vaccine comprising the immunogenic composition of  claim 86 . 
     
     
         88 . The virus of  claim 83 , wherein the virus is a 7:1 reassortant virus, which virus comprises 7 genome segments from one or more donor virus and 1 genome segment comprising a polynucleotide comprising the nucleotide sequence of any one of SEQ ID NO:36-48. 
     
     
         89 . The virus of  claim 83 , wherein the virus is one or more of: a temperature-sensitive virus, a cold-adapted virus, or an attenuated virus. 
     
     
         90 . The virus of  claim 88 , wherein the donor virus is A/Ann Arbor/6/60, B/Ann Arbor/1/66, A/Puerto Rico/8/34, B/Leningrad/14/17/55, B/14/5/1, B/USSR/60/69, B/Leningrad/179/86, B/Leningrad/14/55, or B/England/2608/76. 
     
     
         91 . The virus of  claim 84 , wherein the 6:2 reassortant virus is a live virus. 
     
     
         92 . A method for producing the reassortant influenza virus of  claim 83  comprising:
 introducing a plurality of vectors comprising nucleic acids corresponding to an influenza virus genome into a population of host cells, which influenza virus genome comprises at least 6 internal genome segments of a first influenza strain, and at least one genome segment of a second influenza strain, wherein the at least one genome segment of the second influenza strain comprises a polynucleotide comprising the nucleotide sequence of any one of SEQ ID NO:36-48, and wherein the population of host cells is capable of supporting replication of influenza virus; 
 culturing the population of host cells; and 
 recovering a plurality of influenza viruses. 
 
     
     
         93 . The method of  claim 92 , wherein the first influenza virus strain is at least one of: an attenuated influenza virus strain, a cold-adapted influenza virus strain, and a temperature-sensitive influenza virus strain. 
     
     
         94 . The method of  claim 92 , wherein the influenza viruses are suitable for administration in an intranasal vaccine formulation. 
     
     
         95 . The method of  claim 92 , wherein the influenza virus genome is an influenza A virus genome or influenza B virus genome. 
     
     
         96 . The method of  claim 92 , wherein the first influenza strain is selected from the group consisting of A/Ann Arbor/6/60, B/Ann Arbor/1/66, A/Puerto Rico/8/34, B/Leningrad/14/17/55, B/14/5/1, B/USSR/60/69, B/Leningrad/179/86, B/Leningrad/14/55, or B/England/2608/76. 
     
     
         97 . The method of  claim 92 , wherein the plurality of vectors are plasmid vectors. 
     
     
         98 . The method of  claim 92 , wherein the population of host cells comprises one or more of: Vero cells, cells deposited under ECACC No. 96022940, MDCK cells, 293T cells, or COS cells. 
     
     
         99 . The method of  claim 92 , wherein the method does not comprise use of a helper virus. 
     
     
         100 . The method of  claim 92 , wherein the plurality of vectors consists of eight vectors.

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