Claims for Patent: 9,499,850

Summary for Patent: 9,499,850

Title:	Modified influenza virus for monitoring and improving vaccine efficiency
Abstract:	The immunogenicity of the influenza virus hemagglutinin (HA) molecule may be increased by substitutions of amino acids in the HA sequence. The substitution of specific HA residues, such as asparagine at position 223 of H5 HA, increase the sensitivity of the hemagglutinin inhibition (HI) assay by altering receptor specificity and/or antibody-antigen binding. HA molecules containing such substitutions will be useful in the development of diagnostic reference viruses and improved influenza vaccines.
Inventor(s):	Hoffmann; Erich (Galveston, TX), Lipatov; Aleksandr S. (Atlanta, GA), Webby; Richard J. (Memphis, TN), Govorkova; Elena A. (Cordova, TN), Webster; Robert G. (Memphis, TN)
Assignee:	St. Jude Children\'s Research Hospital (Memphis, TN)
Application Number:	14/045,097
Patent Claims:	1. A method for determining the efficacy of an influenza virus vaccine in a subject, which method comprises reacting antisera derived from the vaccinated subject with a recombinant influenza virus comprising a H5 hemagglutinin (HA) molecule, wherein the HA molecule comprises an asparagine at an amino acid position corresponding to amino acid position 223 in H5 HA and is not an A/HK/213/03 HA molecule, and determining the amount of the virus bound by the antisera. 2. The method of claim 1, wherein the HA molecule is a recombinant HA molecule that comprises one or more amino acid sequence changes as compared to a naturally occurring HA molecule that comprises an amino acid other than asparagine at an amino acid position corresponding to amino acid position 223 in H5 HA. 3. The method of claim 2, wherein the HA molecule has an increased reactivity with antisera derived from a subject exposed to an H5 influenza virus or an H5 influenza vaccine as compared to the naturally occurring HA molecule. 4. A method for increasing the sensitivity of a hemagglutinin inhibition (HI) assay, which method comprises reacting antisera derived from a vaccinated or infected subject with a recombinant influenza virus comprising a H5 hemagglutinin (HA) molecule, wherein the HA molecule comprises an asparagine at an amino acid position corresponding to amino acid position 223 in H5 HA and is not an A/HK/213/03 HA molecule and determining the hemagglutinin inhibition titer. 5. The method of claim 4, which results in at least 2-fold increase in sensitivity of a hemagglutinin inhibition (HI) assay. 6. The method of claim 4, which results in at least 4-fold increase in sensitivity of a hemagglutinin inhibition (HI) assay. 7. The method of claim 4, wherein the HA molecule is a recombinant HA molecule that comprises one or more amino acid sequence changes as compared to a naturally occurring HA molecule that comprises an amino acid other than asparagine at an amino acid position corresponding to amino acid position 223 in H5 HA. 8. A method for determining whether a subject has been exposed to an influenza virus, which method comprises reacting antisera derived from the subject with a recombinant influenza virus comprising a H5 hemagglutinin (HA) molecule, wherein the HA molecule comprises an asparagine at an amino acid position corresponding to amino acid position 223 in H5 HA and is not an A/HK/213/03 HA molecule and determining the amount of the virus bound by the antisera. 9. The method of claim 8, wherein the HA molecule is a recombinant HA molecule that comprises one or more amino acid sequence changes as compared to a naturally occurring HA molecule that comprises an amino acid other than asparagine at an amino acid position corresponding to amino acid position 223 in H5 HA. 10. An isolated nucleic acid encoding a recombinant influenza virus H5 hemagglutinin (HA) molecule, wherein said recombinant H5 HA molecule: (i) comprises one or more amino acid sequence changes as compared to a naturally occurring HA molecule that comprises an amino acid other than asparagine at an amino acid position corresponding to amino acid position 223 in H5 HA; (ii) comprises an asparagine at an amino acid position corresponding to amino acid position 223 in H5 HA; (iii) has an increased reactivity with antisera derived from an animal exposed to an H5 influenza virus or an H5 influenza vaccine as compared to said naturally occurring HA molecule; and (iv) is not A/HK/213/03 HA molecule. 11. A reverse genetics system for making a recombinant influenza virus, wherein said reverse genetics system comprises vectors that express influenza A PB1, PB2, PA, NP, M, NS and NA and a recombinant influenza virus H5 hemagglutinin (HA) molecule, wherein said recombinant H5 HA molecule: (i) comprises one or more amino acid sequence changes as compared to a naturally occurring HA molecule that comprises an amino acid other than asparagine at an amino acid position corresponding to amino acid position 223 in H5 HA; (ii) comprises an asparagine at an amino acid position corresponding to amino acid position 223 in H5 HA; (iii) has an increased reactivity with antisera derived from an animal exposed to an H5 influenza virus or an H5 influenza vaccine as compared to said naturally occurring HA molecule; and (iv) is not A/HK/213/03 HA molecule. 12. A method for making a recombinant influenza virus containing a recombinant influenza virus H5 hemagglutinin (HA) molecule, the method comprises: introducing the reverse genetics system of claim 11 into isolated cells, culturing said cells and isolating the recombinant influenza virus from the cultured cells.

Details for Patent 9,499,850

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Seqirus Vaccines Limited	FLUVIRIN	influenza virus vaccine	Injection	103837	11/03/1998		2025-08-04
Sanofi Pasteur Inc.	FLUZONE, FLUZONE HD QUADRIVALENT, FLUZONE HIGH DOSE, FLUZONE INTRADERMAL, FLUZONE QUADRIVALENT	influenza virus vaccine	Injection	103914	12/09/1999		2025-08-04
Sanofi Pasteur Inc.	FLUZONE, FLUZONE HD QUADRIVALENT, FLUZONE HIGH DOSE, FLUZONE INTRADERMAL, FLUZONE QUADRIVALENT	influenza virus vaccine	Injection	103914	12/23/1909		2025-08-04
Sanofi Pasteur Inc.	FLUZONE, FLUZONE HD QUADRIVALENT, FLUZONE HIGH DOSE, FLUZONE INTRADERMAL, FLUZONE QUADRIVALENT	influenza virus vaccine	Injection	103914	05/09/2011		2025-08-04
Sanofi Pasteur Inc.	FLUZONE, FLUZONE HD QUADRIVALENT, FLUZONE HIGH DOSE, FLUZONE INTRADERMAL, FLUZONE QUADRIVALENT	influenza virus vaccine	Injection	103914	06/07/2013		2025-08-04
Sanofi Pasteur Inc.	FLUZONE, FLUZONE HD QUADRIVALENT, FLUZONE HIGH DOSE, FLUZONE INTRADERMAL, FLUZONE QUADRIVALENT	influenza virus vaccine	Injection	103914	12/11/2014		2025-08-04