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Interleukin-2-leukotoxin gene fusions and uses thereof |
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| The practice of the present invention will employ, unless otherwise indicated, conventional ... |
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GnRH-leukotoxin chimeras |
| The practice of the present invention will employ, unless otherwise indicated, conventional ... |
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GNRH-leukotoxin chimeras |
| The practice of the present invention will employ, unless otherwise indicated, conventional ... |
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Polynucleotides encoding LKT 111 |
| The practice of the present invention will employ, unless otherwise indicated, conventional ... |
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Methods and compositions for the treatment of defects in lipoprotein metabolism |
| In one aspect, the invention provides a recombinant viral vector comprising the DNA of, or ... |
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Antisera against a PEB1 antigen from Campylobacter jejuni |
| It is an object of the present invention to provide highly specific and highly sensitive diagnostic ... |
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Gene encoding invasion protein of campylobacter species |
| OF PREFERRED EMBODIMENTS The following standard abbreviations for the amino acid residues are used ... |
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Preservatives for vaccines |
| New combinations of preservatives that pass antimicrobial testing requirements for United States P... |
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Recombinant parainfluenza virus expression system and vaccines
| Details |
Inventors: Haller, Aurelia; Coelingh, Kathleen L.;
Assignee: MedImmune Vaccines, Inc. (Mountain View, CA)
Primary Examiner: Salimi; Ali R.
Assistant Examiner:
Attorney, Agent or Firm: Jones Day
The present invention relates to recombinant bovine parainfluenza virus (bPIV) cDNA or RNA which may be used to express heterologous gene products in appropriate host cell systems and/or to rescue negative strand RNA recombinant viruses that express, package, and/or present the heterologous gene product. The chimeric viruses and expression products may advantageously be used in vaccine formulations including vaccines against a broad range of pathogens and antigens. |
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DETAILED DESCRIPTION What is claimed is: 1. An immunogenic formulation comprising a chimeric parainfluenza virus comprising (i) nucleotide sequences of Kansas-strain bovine parainfluenza virus type 3 genome comprising nucleotides 1-5041 and nucleotides 8529-15,456 of the genome of Kansas strain bovine parainfluenza virus type 3; and (ii) F and HN gene sequences of human parainfluenza virus type 3. 2. An immunogenic formulation comprising a chimeric parainfluenza virus comprising: (i) nucleotide sequences of Kansas-strain bovine parainfluenza virus type 3 genome; and (ii) the F and HN gene sequences of human parainfluenza virus type 3, wherein (i) PCR amplification of nucleotide 5,255 to 6,255 of the chimeric parainfluenza virus results in a DNA fragment that is recognized by restriction endonucleases Sac I and Bgl II; and (ii) PCR amplification of nucleotide 9,075 to 10,469 of the chimeric parainfluenza virus results in a DNA fragment that is recognized by restriction endonucleases Pvu II and Bam HI. 3. An immunogenic formulation comprising a chimeric parainfluenza virus comprising (i) nucleotide sequences of Kansas-strain bovine parainfluenza virus type 3 genome comprising nucleotides 1-5041 and nucleotides 8529-15,456 of the genome of Kansas strain bovine parainfluenza virus type 3; and (ii) one or more sequences derived from RSV, Ply, New Castle Disease virus, Sendai virus, Infectious Laryngotracheitis virus or influenza. 4. An immunogenic formulation comprising a chimeric parainfluenza virus comprising: (i) nucleotide sequences of Kansas-strain bovine parainfluenza virus type 3 genome comprising nucleotides 1-5041 of the genome of Kansas-strain bovine parainfluenza virus type 3; and (ii) one or more sequences derived from RSV, PIV, New Castle Disease virus, Sendai virus, infectious Laryngotracheitis virus or influenza. 5. An immunogenic formulation comprising a chimeric parainfluenza virus comprising: (i) nucleotide sequences of Kansas-strain bovine parainfluenza virus type 3 genome; and (ii) one or more sequences derived from RSV, PIV, New Castle Disease virus, Sendai virus, Infectious Laryngotracheitis virus or influenza, and wherein said sequences have been added at a nucleotide position of Kansas-strain bovine parainfluenza virus type 3 selected from the group consisting of nucleotide position 5041, the HN gene, and nucleotide position 8529
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