Patent classifications
C07K14/235
Correlation of disease activity with clonal expansions of human papillomavirus 16-specific CD8+ T-cells in patients with severe erosive oral lichen planus
A massive clonal expansion of activated CD8.sup.+ T-cells with increased frequency of HPV 16-specific CD8.sup.+ T-cells was discovered to be a characteristic of oral lichen planus (OLP), indicating a causal link between HPV infection and the dysimmune process. The invention relates to compositions and methods for the diagnosis and treatment of OLP patients.
Methods and compositions related to the next generation vaccine
Disclosed are compositions comprising a Gram negative needle tip protein and a translocator protein and methods of their use.
Methods and compositions related to the next generation vaccine
Disclosed are compositions comprising a Gram negative needle tip protein and a translocator protein and methods of their use.
OMPA MUTATIONS ENHANCE OMV PRODUCTION IN BORDETELLA PERTUSSIS
The invention pertains to a mutant Bordetella OmpA polypeptide. A Bordetella comprising said mutant polypeptide has a high blebbing phenotype. Hence, the invention further pertains a method for producing OMVs, wherein the method comprises a step of culturing a population of Bordetella bacteria comprising a modified OmpA polypeptide, under conditions conductive for the production of OMVs. In addition, the invention pertains to OMVs produced by a Bordetella comprising a mutant OmpA polypeptide, and the use of such OMVs for the treatment and prevention of a Bordetella infection.
OMPA MUTATIONS ENHANCE OMV PRODUCTION IN BORDETELLA PERTUSSIS
The invention pertains to a mutant Bordetella OmpA polypeptide. A Bordetella comprising said mutant polypeptide has a high blebbing phenotype. Hence, the invention further pertains a method for producing OMVs, wherein the method comprises a step of culturing a population of Bordetella bacteria comprising a modified OmpA polypeptide, under conditions conductive for the production of OMVs. In addition, the invention pertains to OMVs produced by a Bordetella comprising a mutant OmpA polypeptide, and the use of such OMVs for the treatment and prevention of a Bordetella infection.
METHODS AND COMPOSITIONS RELATED TO THE NEXT GENERATION VACCINE
Disclosed are compositions comprising a Gram negative needle tip protein and a translocator protein and methods of their use.
METHODS AND COMPOSITIONS RELATED TO THE NEXT GENERATION VACCINE
Disclosed are compositions comprising a Gram negative needle tip protein and a translocator protein and methods of their use.
Bordetella T Cells Epitopes, Megapools and Uses Thereof
The present invention includes compositions, including epitope megapools, and methods for detecting the presence of: a Bordetella or an immune response relevant to a Bordetella infection including T cells responsive to one or more Bordetella peptides or proteins comprising, consisting of, or consisting essentially of: one or more amino acid sequences, fusion proteins, a pool of 2 or more peptides, or polynucleotides that expression the amino acid sequences selected from those set forth in any one of Tables 1-20 (SEQ ID NOS: 1 to 2598). The invention further provides vaccines, diagnostics, therapies, and kits, comprising such proteins or peptides.
Bordetella T Cells Epitopes, Megapools and Uses Thereof
The present invention includes compositions, including epitope megapools, and methods for detecting the presence of: a Bordetella or an immune response relevant to a Bordetella infection including T cells responsive to one or more Bordetella peptides or proteins comprising, consisting of, or consisting essentially of: one or more amino acid sequences, fusion proteins, a pool of 2 or more peptides, or polynucleotides that expression the amino acid sequences selected from those set forth in any one of Tables 1-20 (SEQ ID NOS: 1 to 2598). The invention further provides vaccines, diagnostics, therapies, and kits, comprising such proteins or peptides.
Fermentation process
The present invention relates to processes for Bordetella fermentation and virulence factor production, especially PT production, for large scale manufacturing. More particularly, processes including a medium conditioning step carried out prior to inoculation.