The present invention contemplates therapeutic compositions containing a fibrinogen homolog capable of binding to endothelial cells in an RGD-independent manner that inhibits fibrinogen binding to endothelial cells. Also described are therapeutic compositions containing an ICAM-1 homolog capable of binding to fibrinogen in an RGD-independent manner that inhibits fibrinogen binding to endothelial cells. Methods of inhibiting endothelial cell and fibrinogen mediated inflammation within a patient by administering a homolog of this invention are also contemplated.
Methods For Inhibiting Endothelial Cell And Fibrinogen Mediated Inflammation Using Fibrinogen Specific Antibodies
The present invention contemplates therapeutic compositions containing a fibrinogen homolog capable of binding to endothelial cells in an RGD-independent manner that inhibits fibrinogen binding to endothelial cells. Also described are therapeutic compositions containing an ICAM-1 homolog capable of binding to fibrinogen in an RGD-independent manner that inhibits fibrinogen binding to endothelial cells. Methods of inhibiting endothelial cell and fibrinogen mediated inflammation within a patient by administering a homolog of this invention are also contemplated.
T Cell Epitopes Of The Hepatitis B Virus Nucleocapsid Protein
George B. Thornton - San Diego CA Ann M. Moriarty - San Diego CA David R. Milich - San Diego CA Alan McLachlan - San Diego CA
Assignee:
Scripps Clinic and Research Foundation - La Jolla CA
International Classification:
A61K 3900 A61K 3929 C07K 700 C07K 1500
US Classification:
424 88
Abstract:
Polypeptides corresponding in amino acid residue sequence to T cell stimulating regions of the HBV nucleocapsid protein are disclosed. A method of enhancing the immunogenicity of a polypeptide immunogen comprising operatively linking the polypeptide through an amino acid residue side chain to core protein particles is also disclosed.
T Cell Epitopes Of The Hepatitis B Virus Nucleocapsid Protein
George B. Thornton - San Diego CA Ann M. Moriarty - San Diego CA David R. Milich - San Diego CA Alan McLachlan - San Diego CA
Assignee:
The Scripps Research Institute - La Jolla CA
International Classification:
A61K 3900 A61K 3929 C07K 700 C07K 1500
US Classification:
424 88
Abstract:
Polypeptides corresponding in amino acid residue sequence to T cell stimulating regions of the HBV nucleocapsid protein are disclosed. A method of enhancing the immunogenicity of a polypeptide immunogen comprising operatively linking the polypeptide through an amino acid residue side chain to core protein particles is also disclosed.
Methods And Compositions For Inhibiting Endothelial Cell And Fibrinogen Mediated Inflammation
Dario C. Altieri - La Jolla CA Lucia R. Languino - La Jolla CA George B. Thornton - Ramona CA
Assignee:
The Scripps Research Institute - La Jolla CA
International Classification:
C07K 1600
US Classification:
5303879
Abstract:
The present invention contemplates therapeutic compositions containing a fibrinogen homolog capable of binding to endothelial cells in an RGD-independent manner that inhibits fibrinogen binding to endothelial cells. Also described are therapeutic compositions containing an ICAM-1 homolog capable of binding to fibrinogen in an RGD-independent manner that inhibits fibrinogen binding to endothelial cells. Methods of inhibiting endothelial cell and fibrinogen mediated inflammation within a patient by administering a homolog of this invention are also contemplated.
T Cell Epitopes Of The Hepatitis B Virus Nucleocapsid Protein
George B. Thornton - San Diego CA Ann M. Moriarty - San Diego CA David R. Milich - San Diego CA Alan McLachlan - San Diego CA
Assignee:
Scripps Clinic and Research Foundation - La Jolla CA
International Classification:
A61K 3900 A61K 3929 C07K 700 C07K 1500
US Classification:
424 88
Abstract:
Polypeptides corresponding in amino acid residue sequence to T cell stimulating regions of the HBV nucleocapsid protein are disclosed. A method of enhancing the immunogenicity of a polypeptide immunogen comprising operatively linking the polypeptide through an amino acid residue side chain to core protein particles is also disclosed.
Fibrinogen .Gamma. Chain Polypeptide And Compositions Thereof
Dario C. Altieri - La Jolla CA Lucia R. Languino - La Jolla CA George B. Thornton - Ramona CA
Assignee:
The Scripps Research Institute - La Jolla CA
International Classification:
A61K 3803 A61K 3810
US Classification:
514 8
Abstract:
The present invention contemplates therapeutic compositions containing a fibrinogen homolog capable of binding to endothelial cells in an RGD-independent manner that inhibits fibrinogen binding to endothelial cells. Also described are therapeutic compositions containing an ICAM-1 homolog capable of binding to fibrinogen in an RGD-independent manner that inhibits fibrinogen binding to endothelial cells. Methods of inhibiting endothelial cell and fibrinogen mediated inflammation within a patient by administering a homolog of this invention are also contemplated.
Method Of Inhibiting Fibrinogen Binding To Endothelial Cells With Fibrinogen Gamma Chain Peptides
Dario C. Altieri - La Jolla CA Lucia R. Languino - La Jolla CA George B. Thornton - Ramona CA
Assignee:
The Scripps Research Institute - La Jolla CA
International Classification:
A61K 3802 A61K 3817
US Classification:
514 2
Abstract:
The present invention contemplates therapeutic compositions containing a fibrinogen homolog capable of binding to endothelial cells in an RGD-independent manner that inhibits fibrinogen binding to endothelial cells. Also described are therapeutic compositions containing an ICAM-1 homolog capable of binding to fibrinogen in an RGD-independent manner that inhibits fibrinogen binding to endothelial cells. Methods of inhibiting endothelial cell and fibrinogen mediated inflammation within a patient by administering a homolog of this invention are also contemplated.