Eli Lilly and Company

Stuart W Bright

Anne H Dantzig

Linda B Tabas

Kristine Kay Kikly

Catherine Brautigam Beidler

Daniel Scott Girard

Alain Philippe Vasserot

David Matthew Marquis

Julian Davies

Craig Duane Dickinson

Karen L Cox

Oliver Schroeder

John R Sportsman

Andrea Paula Martin

Sean Edward Sissons

Xiao-Fen Wang

Angus John MacDonald

Joshua Dade Poorbaugh

Scott W Sage

Gerald Gold

Provided are antibodies, or an antigen-binding fragment thereof, that binds human IL-21, These antibodies are useful in immunoassays of IL-21 levels, and/or in vivo, ex vivo or in vitro immunochemical and other imaging methods for determining the presence of IL-21 and/or quantifying IL-21 levels, and for diagnostic, prognostic and predictive purpose, and or optimizing therapeutic regimens in patients in which IL-21 signaling is implicated in pathogenesis.

Methods of detecting human IL-21

The present invention provides an antibody that binds to the p19 subunit of human IL-23 and is characterized as having high affinity, selective, and neutralizing properties. The antibody is useful in the treatment or prevention of an autoimmune or inflammatory condition selected from the group consisting of consisting of multiple sclerosis, rheumatoid arthritis, psoriasis, inflammatory bowel diseases, ankylosing spondylitis, graft-versus-host disease, lupus and metabolic syndrome. The antibody is also useful in the treatment of cancer.

Nucleic acids encoding antibodies that bind IL-23

Antibodies that bind to IL-23

The present invention encompasses isolated antibodies, or antigen-binding portions thereof, that specifically bind to the p19 subunit of IL-23. These antibodies, or antigen-binding portions thereof, are high affinity, neutralizing antibodies useful for the treatment of autoimmune disease.

Anti-IL-23 antibodies

Monoclonal antibodies which react with the human influx peptide transporter are provided. The human influx peptide transporter-reactive antibodies are useful in the purification of influx peptide transporter and in immunoassays to identify agents taken up into the cell by the human influx peptide transporter mechanism.

Immunomethods for isolating and indentifying human influx peptide transporter

Monoclonal antibodies which react with the human influx peptide transporter are provided. The human influx peptide transporter-reactive antibodies are useful in the purification of influx peptide transporter and in immunoassays to identify agents taken up into the cell by the human influx peptide transporter mechanism. The monoclonal antibodies are also useful for the detection and treatment of carcinomas derived from the gastrointestinal tract and pancreatic duct.

Diagnosis of colon carcinoma using monoclonal antibodies to human influx

Monoclonal antibodies to human influx peptide transporter

Methods have been developed to produce novel compounds by covalently coupling thiazolidinedione insulin sensitivity enhancers (ISEs) to proteins. These novel compounds are well suited for producing antibodies, which are specific for thiazolidinedione ISEs and which are well suited for fluorescent immunoassays of thiazolidinedione and non-thiazolidinedione ISEs in buffers and biological tissues. Antibodies also are well suited for high-volume screening for immunologically related novel, non-thiazolidinedione and thiazolidinedione ISEs.

Immunoassays for insulin sensitivity enhancers, insulin sensitivity

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Indianapolis, IN, United States of America

Stuart W Bright