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US Patent Application 20090010962 - Genetically Engineered Swine Influenza Virus and Uses Thereof

 
June 1, 2005
User ID: 758380
United States
11/09/2009 11:51 PM
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US Patent Application 20090010962 - Genetically Engineered Swine Influenza Virus and Uses Thereof
attenuated swine influenza virus comprising a mutation in a swine influenza NS1 gene that diminishes the ability of the NS1 gene product to antagonize the cellular interferon response, and permits the attenuated virus, at a multiplicity of infection of 0.001, to grow to titers between approximately 3 fold to approximately 7 fold lower than wild-type swine influenza in pig cells, as determined approximately 5 days post-infection when propagated under the same conditions.

2. The attenuated swine influenza virus of claim 1, wherein the attenuated virus is genetically engineered.

3. The attenuated swine influenza virus of claim 1, wherein the attenuated virus is a mutagenized virus or reassortant.

4. The attenuated swine influenza virus of claim 2, wherein the attenuated virus is a chimeric virus that expresses a heterologous sequence.

5. The attenuated swine influenza virus of claim 2, wherein the attenuated virus is a chimeric virus that expresses a tumor antigen.

6. The attenuated swine influenza virus of claim 2, wherein the attenuated virus is a chimeric virus that expresses an epitope of a foreign pathogen.

7. The attenuated swine influenza virus of claim 1, wherein pig cells are PK(D1) cells, PK(15) cells, PK13 cells, NSK cells, LLC-PK1 cells, LLC-PK1A cells, ESK-4 cells, ST cells, PT-K75 cells, PK-2a/CL 13 cells or SJPL cells.

8. (canceled)

9. The attenuated swine influenza virus of claim 2, wherein the mutation is a deletion at the carboxy terminus of the NS1 gene.

10. (canceled)

11. An attenuated swine influenza virus comprising a modified NS1 gene, wherein the attenuated swine influenza virus is TX/98/del 126, TX/98/del 99 or TX/98/del 73.

12. An attenuated swine influenza virus having an altered interferon antagonist phenotype, wherein said virus comprises a mutation in the NS1 gene resulting in a deletion of between the 105 carboxy terminal amino acid residues and the 160 carboxy terminal amino acid residues of NS1.

13. The attenuated swine influenza virus of claim 12, wherein the virus is attenuated by a mutation in the NS1 gene resulting in a deletion of all of the amino acid residues of NS1 except amino acid residues 1-95, amino acid residues 1-90, amino acid residues 1-85, amino acid residues 1-80, amino acid residues 1-75, amino acid residues 1-73, amino acid residues 1-70, amino acid residues 1-65, or amino acid residues 1-60, and wherein the amino terminal amino acid is number 1 and the mutation in the NS1 gene confers an altered interferon antagonist phenotype.

14. (canceled)

15. A immunogenic formulation comprising the attenuated swine influenza virus of claim 1, and a physiologically acceptable excipient.

16. A immunogenic formulation comprising the attenuated swine influenza virus of claim 11 or 12, and a physiologically acceptable excipient.

17. A pharmaceutical formulation comprising the attenuated swine influenza virus of claim 1, and a physiologically acceptable excipient.

18. A pharmaceutical formulation comprising the attenuated swine influenza virus of claim 11 or 12, and a physiologically acceptable excipient.

19-20. (canceled)

21. The immunogenic formulation of claim 15, wherein the attenuated swine influenza virus is genetically engineered.

22. The immunogenic formulation of claim 21, wherein the attenuated swine influenza virus is a chimeric virus that expresses a heterologous sequence.

23-26. (canceled)

27. The pharmaceutical formulation of claim 17, wherein the attenuated swine influenza virus is genetically engineered.

28-29. (canceled)

30. The pharmaceutical formulation of claim 27, wherein the attenuated swine influenza virus is a chimeric virus that expresses a tumor antigen.

31. A method for immunizing or inducing an immune response in a pig, comprising administering to said pig an effective amount of the immunogenic formulation of claim 21.

32. A method for immunizing or inducing an immune response a pig, comprising administering to said pig an effective amount of the immunogenic formulation of claim 16.

33. A method of treating a swine influenza virus infection in a pig, comprising administering to said pig an effective amount of the pharmaceutical formulation of claim 27.

34. A method of treating a swine influenza virus infection in a pig, comprising administering to said pig an effective amount of the pharmaceutical formulation of claim 18.

35. A method of treating cancer in a pig, comprising administering to said pig an effective amount of the pharmaceutical formulation of claim 30.

36-40. (canceled)

41. A method for production of an immunogenic formulation comprising:(a) propagating in a substrate the attenuated swine influenza virus of claim 1; and(b) collecting progeny virus,wherein the substrate is a cell, cell line or embryonated egg.

42. A method for production of an immunogenic formulation comprising:(a) propagating in a substrate the attenuated swine influenza virus of claim 11 or 12;(b) collecting progeny virus;wherein the substrate is a cell, cell line or embryonated egg.

43-56. (canceled)

57. A cell containing the attenuated swine influenza virus of claim 1.

58. (canceled)

59. A cell containing the swine influenza virus of claim 11 or 12.

60-69. (canceled)

70. An embryonated egg containing the attenuated swine influenza virus of claim 1.

71-77. (canceled)

[link to www.patentstorm.us]
Anonymous Coward (OP)
User ID: 758380
United States
11/09/2009 11:57 PM
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Re: US Patent Application 20090010962 - Genetically Engineered Swine Influenza Virus and Uses Thereof
Inventors
Palese, Peter
Garcia-Sastre, Adolfo
Webby, Richard J.
Richt, Juergen A.
Webster, Robert G.
Lager, Kelly M.
Anonymous Coward
User ID: 793040
United States
11/10/2009 12:44 AM
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Re: US Patent Application 20090010962 - Genetically Engineered Swine Influenza Virus and Uses Thereof
trans_sign
AardwarkianSurmise
User ID: 817728
United States
11/13/2009 05:25 PM
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Re: US Patent Application 20090010962 - Genetically Engineered Swine Influenza Virus and Uses Thereof
So I was pondering the #'s on this thing and it dawned on me that with a bit of rearranging they add up to a significant date in history, with an extra 006 meaning god knows what yoda
Anonymous Coward
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United States
11/13/2009 05:26 PM
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Re: US Patent Application 20090010962 - Genetically Engineered Swine Influenza Virus and Uses Thereof
It's a method to make vaccines, so what?
messageinlightbulb"DJ​ED P
User ID: 807933
United States
11/13/2009 07:29 PM
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Re: US Patent Application 20090010962 - Genetically Engineered Swine Influenza Virus and Uses Thereof
attenuated swine influenza virus comprising a mutation in a swine influenza NS1 gene that diminishes the ability of the NS1 gene product to antagonize the cellular interferon response, and permits the attenuated virus, at a multiplicity of infection of 0.001, to grow to titers between approximately 3 fold to approximately 7 fold lower than wild-type swine influenza in pig cells, as determined approximately 5 days post-infection when propagated under the same conditions.

2. The attenuated swine influenza virus of claim 1, wherein the attenuated virus is genetically engineered.

3. The attenuated swine influenza virus of claim 1, wherein the attenuated virus is a mutagenized virus or reassortant.

4. The attenuated swine influenza virus of claim 2, wherein the attenuated virus is a chimeric virus that expresses a heterologous sequence.

5. The attenuated swine influenza virus of claim 2, wherein the attenuated virus is a chimeric virus that expresses a tumor antigen.

6. The attenuated swine influenza virus of claim 2, wherein the attenuated virus is a chimeric virus that expresses an epitope of a foreign pathogen.

7. The attenuated swine influenza virus of claim 1, wherein pig cells are PK(D1) cells, PK(15) cells, PK13 cells, NSK cells, LLC-PK1 cells, LLC-PK1A cells, ESK-4 cells, ST cells, PT-K75 cells, PK-2a/CL 13 cells or SJPL cells.

8. (canceled)

9. The attenuated swine influenza virus of claim 2, wherein the mutation is a deletion at the carboxy terminus of the NS1 gene.

10. (canceled)

11. An attenuated swine influenza virus comprising a modified NS1 gene, wherein the attenuated swine influenza virus is TX/98/del 126, TX/98/del 99 or TX/98/del 73.

12. An attenuated swine influenza virus having an altered interferon antagonist phenotype, wherein said virus comprises a mutation in the NS1 gene resulting in a deletion of between the 105 carboxy terminal amino acid residues and the 160 carboxy terminal amino acid residues of NS1.

13. The attenuated swine influenza virus of claim 12, wherein the virus is attenuated by a mutation in the NS1 gene resulting in a deletion of all of the amino acid residues of NS1 except amino acid residues 1-95, amino acid residues 1-90, amino acid residues 1-85, amino acid residues 1-80, amino acid residues 1-75, amino acid residues 1-73, amino acid residues 1-70, amino acid residues 1-65, or amino acid residues 1-60, and wherein the amino terminal amino acid is number 1 and the mutation in the NS1 gene confers an altered interferon antagonist phenotype.

14. (canceled)

15. A immunogenic formulation comprising the attenuated swine influenza virus of claim 1, and a physiologically acceptable excipient.

16. A immunogenic formulation comprising the attenuated swine influenza virus of claim 11 or 12, and a physiologically acceptable excipient.

17. A pharmaceutical formulation comprising the attenuated swine influenza virus of claim 1, and a physiologically acceptable excipient.

18. A pharmaceutical formulation comprising the attenuated swine influenza virus of claim 11 or 12, and a physiologically acceptable excipient.

19-20. (canceled)

21. The immunogenic formulation of claim 15, wherein the attenuated swine influenza virus is genetically engineered.

22. The immunogenic formulation of claim 21, wherein the attenuated swine influenza virus is a chimeric virus that expresses a heterologous sequence.

23-26. (canceled)

27. The pharmaceutical formulation of claim 17, wherein the attenuated swine influenza virus is genetically engineered.

28-29. (canceled)

30. The pharmaceutical formulation of claim 27, wherein the attenuated swine influenza virus is a chimeric virus that expresses a tumor antigen.

31. A method for immunizing or inducing an immune response in a pig, comprising administering to said pig an effective amount of the immunogenic formulation of claim 21.

32. A method for immunizing or inducing an immune response a pig, comprising administering to said pig an effective amount of the immunogenic formulation of claim 16.

33. A method of treating a swine influenza virus infection in a pig, comprising administering to said pig an effective amount of the pharmaceutical formulation of claim 27.

34. A method of treating a swine influenza virus infection in a pig, comprising administering to said pig an effective amount of the pharmaceutical formulation of claim 18.

35. A method of treating cancer in a pig, comprising administering to said pig an effective amount of the pharmaceutical formulation of claim 30.

36-40. (canceled)

41. A method for production of an immunogenic formulation comprising:(a) propagating in a substrate the attenuated swine influenza virus of claim 1; and(b) collecting progeny virus,wherein the substrate is a cell, cell line or embryonated egg.

42. A method for production of an immunogenic formulation comprising:(a) propagating in a substrate the attenuated swine influenza virus of claim 11 or 12;(b) collecting progeny virus;wherein the substrate is a cell, cell line or embryonated egg.

43-56. (canceled)

57. A cell containing the attenuated swine influenza virus of claim 1.

58. (canceled)

59. A cell containing the swine influenza virus of claim 11 or 12.

60-69. (canceled)

70. An embryonated egg containing the attenuated swine influenza virus of claim 1.

71-77. (canceled)

[link to www.patentstorm.us]
 Quoting: June 1, 2005 758380
The bird flu-swine flu="BLACK BIRD BONE EXPOSIER" could not filter as i took its right wing down,they landed on djed pillars=mountain of communication and cleansing,This made it air born,it was technology fighting for the highest form of communication,think were you get them phone frequencies,for there are many sights of the earth but none greater than the great Giza,although the great pyramid remains only the shadow of this operation.

many alignments of the earth in light seconds,as carved in stone Rosetta,hieroglyphics.if the reader will do its fourth place math of definition DEC 21,2006.

mountain forms global in many pieces of communication,as per carved in stone,your nation is some 3,500 years behind in this light knowledge,ancient helicopter,when they broke up mountain formation trying to land of the helicopter it broke its ability to cleanse your chemicals,your nations sickness started to this effect.by now you have heard of the white powder that grows back body parts,its real my friend,it comes from great mountain,this is your number one problem of the entire globe,


i will wait for the debunk er of this knowledge.i remain lightson tah.
Anonymous Coward
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Canada
11/13/2009 07:53 PM
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Re: US Patent Application 20090010962 - Genetically Engineered Swine Influenza Virus and Uses Thereof
bump burnit yoda
AardwarkinSurmise
User ID: 817728
United States
11/13/2009 08:22 PM
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Re: US Patent Application 20090010962 - Genetically Engineered Swine Influenza Virus and Uses Thereof
just had another look its not 006 after all
god help us...
fido

User ID: 835694
Pakistan
12/07/2009 02:54 PM
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Re: US Patent Application 20090010962 - Genetically Engineered Swine Influenza Virus and Uses Thereof
Who's at High Risk From Swine Flu?

In Mexico, the virus appears to be targeting those aged 20 to 40. This is not unusual – the same occurred during the worst pandemic of the last century, in 1918, when 20 to 40 million people died. Young healthy people with strong immune systems react most powerfully to the virus but the very strength of their reaction produces inflammation and secretions in the lungs which can be overwhelming. In the US, the virus appears to be targeting children who are suffering only mild illness. The difference in the two countries is so far unexplained. One hypothesis is that a second virus may be circulating in Mexico which is interacting with the swine flu virus to produce more severe symptoms.

[link to swine-h1n1virus.blogspot.com]





GLP