Abstract:
The present application relates to isolated proteins, particularly monoclonal antibodies, in particular CDR-grafted, humanized antibodies which bind to RAGE protein. Specifically, these antibodies have the ability to inhibit the binding of RAGE to its various ligands. The antibodies or portions thereof of described in the present application are useful for treating a disease or disorder characterized by or induced by pathophysiological ligands of RAGE, for example missfolded proteins like amyloid ß and advanced glycation-end-products.
Abstract:
The subject invention relates to isolated proteins, particularly monoclonal antibodies, which bind to the Nogo-66 receptor. Specifically, these antibodies have the ability to inhibit the binding of the natural ligand of the Nogo-66 receptor and neutralize the Nogo-66 receptor. These antibodies or portions thereof of the invention are useful for detecting NgR and for inhibiting NgR activity, for example in a human suffering from a disorder in which NgR or Nogo-66 activity is detrimental.
Abstract:
The subject invention relates to isolated proteins, particularly monoclonal antibodies, which bind to the Nogo-66 receptor. Specifically, these antibodies have the ability to inhibit the binding of the natural ligand of the Nogo-66 receptor and neutralize the Nogo-66 receptor. These antibodies or portions thereof of the invention are useful for detecting NgR and for inhibiting NgR activity, for example in a human suffering from a disorder in which NgR or Nogo-66 activity is detrimental.
Abstract:
The subject invention relates to isolated proteins, particularly monoclonal antibodies, which bind and neutralize RGM A protein. Specifically, these antibodies have the ability to inhibit the binding of RGM A to its receptor and/or coreceptors. These antibodies or portions thereof of the invention are useful for detecting RGM A and for inhibiting RGM A activity, for example in a human suffering from a disorder including but not limited to multiple sclerosis, mammalian brain trauma, spinal cord injury, stroke, neurodegenerative diseases, and schizophrenia.
Abstract:
Disclosed is an isolated antibody comprising an antigen binding domain, said antibody capable of binding an epitope of a RGM molecule, said antigen binding domain comprising a heavy chain variable domain having at least three complementary determining regions and a light chain variable domain having at least three complementary determining regions, wherein the at least three complementary determining regions of the heavy chain variable domain have the amino acid sequence of SEQ ID NO:57, SEQ ID NO:58 and SEQ ID NO:59 and the at least three complementary determining regions of the light chain variable domain have the amino acid sequence of SEQ ID NO: 60, SEQ ID NO:61 and SEQ ID NO:62. Further disclosed is an isolated antibody comprising an antigen binding domain, said antibody capable of binding an epitope of a RGM molecule, said antigen binding domain comprising a heavy chain variable domain and a light chain variable wherein the heavy chain variable domain has the amino acid sequence selected from the group consisting of: SEQ ID NOS: 35, 36, 37, 38, 39, 40, 41, 42, 43, 47, 48, 49 and 50 and wherein the light chain variable domain has the amino acid sequence selected from the group consisting of SEQ ID NO:44, 45, 46, 51, 52, 53 and 54.
Abstract:
Proteínas aisladas, particularmente anticuerpos monoclonales, que se unen y neutralizan la proteína RGM A. Específicamente, estos anticuerpos tienen la capacidad de inhibir la unión de RGM A a su receptor y/o sus correceptores. Los anticuerpos de la invención, o sus porciones, son útiles para detectar RGM A e inhibir la actividad de RGM A, por ejemplo, en un ser humano afectado por un trastorno que incluye, no taxativamente, esclerosis múltiple, traumatismo cerebral en mamíferos, lesiones en la médula espinal, accidente cerebrovascular, enfermedades neurodegenerativas, y esquizofrenia.
Abstract:
The subject invention relates to monoclonal antibodies which bind and neutralize RGM A protein. Specifically, these antibodies have the ability to inhibit the binding of RGM A to its receptor and/or coreceptors. These antibodies or antigen binding fragments thereof of the invention are useful for detecting RGM A and for inhibiting RGM A activity, for example in a human suffering from a disorder including but not limited to multiple sclerosis, mammalian brain trauma, spinal cord injury, stroke, neurodegenerative diseases, and schizophrenia.
Abstract:
The subject invention relates to isolated proteins, particularly monoclon al antibodies, which bind to the Nogo-66 receptor. Specifically, these antib odies have the ability to inhibit the binding of the natural ligand of the N ogo-66 receptor and neutralize the Nogo-66 receptor. These antibodies or por tions thereof of the invention are useful for detecting NgR and for inhibiti ng NgR activity, for example in a human suffering from a disorder in which N gR or Nogo-66 activity is detrimental.
Abstract:
Un anticuerpo monoclonal neutralizante aislado, o un fragmento de unión al antígeno del mismo, que interactúan específicamente al menos con un epítopo del receptor de Nogo-66, donde el anticuerpo monoclonal neutralizante aislado, o un fragmento de unión al antígeno del mismo , comprende una secuencia que comprende una región variable de cadena pesada (región VH) que comprende SEQ ID NO: 3 y una secuencia que comprende una región variable de cadena ligera (región VL) que comprende SEQ ID NO: 4, o una secuencia que comprende una región variable de cadena pesada (región VH) que comprende SEQ ID NO: 5 y una secuencia que comprende una región variable de cadena ligera (región VL) que comprende SEQ ID NO: 6.
Abstract:
The present application relates to isolated proteins, particularly monoclonal antibodies, in particular CDR-grafted, humanized antibodies which bind to RAGE protein. Specifically, these antibodies have the ability to inhibit the binding of RAGE to its various ligands. The antibodies or portions thereof of described in the present application are useful for treating a disease or disorder characterized by or induced by pathophysiological ligands of RAGE, for example missfolded proteins like amyloid and advanced glycation-end-products.No suitable figure