Methods for inhibiting lymphotoxin beta receptor signalling
AssigneeBiogen Idec MA Inc.
InventorsJeffrey Browning, Christopher Benjamin, Paula Hochman
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AssigneeBiogen Idec MA Inc.
InventorsJeffrey Browning, Christopher Benjamin, Paula Hochman
Estimating the term…
This invention relates to compositions and methods comprising “lymphotoxin-β receptor blocking agents”, which block lymphotoxin-β receptor signalling. Lymphotoxin-β receptor blocking agents are useful for treating lymphocyte-mediated immunological diseases, and more particularly, for inhibiting Th1 cell-mediated immune responses. This invention relates to soluble forms of the lymphotoxin-β receptor extracellular domain that act as lymphotoxin-β receptor blocking agents. This invention also relates to the use of antibodies directed against either the lymphotoxin-β receptor or its ligand, surface lymphotoxin, that act as lymphotoxin-β receptor blocking agents. A novel screening method for selecting soluble receptors, antibodies and other agents that block LT-β receptor signalling is provided.
A method for treating or reducing the advancement, severity or effects of an immunological disease in an animal comprising the step of administering a pharmaceutical composition which comprises a therapeutically effective amount of a LT-β-R blocking agent and a pharmaceutically acceptable carrier.
A method for inhibiting a Th1 cell-mediated immune response in an animal comprising the step of administering a pharmaceutical composition which comprises an effective amount of a LT-β-R blocking agent and a pharmaceutically effective carrier.
A pharmaceutical composition comprising a therapeutically effective amount of a LT-β-R blocking agent and a pharmaceutically acceptable carrier.
A method for selecting a LT-β-R blocking agent comprising the steps of:
A method for inhibiting LT-β-R signalling without inhibiting TNF-R signalling comprising the step of administering to a subject an effective amount of a LT-β-R blocking agent.
A method of treating inflammatory bowel syndrome comprising administering a therapeutically effective amount of an LT-β-R fusion protein.
Dependencies are inferred from the claim text.