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The Journal of Immunology, 1999, 163: 5173-5177.
Copyright © 1999 by The American Association of Immunologists


CUTTING EDGE

Cutting Edge: A Small Molecule Antagonist of LFA-1-Mediated Cell Adhesion

Terence A. Kelly1, Deborah D. Jeanfavre, Daniel W. McNeil, Joseph R. Woska, Jr., Patricia L. Reilly, Elizabeth A. Mainolfi, Karen M. Kishimoto, Gerald H. Nabozny, Rosemarie Zinter, Barbara-Jean Bormann and Robert Rothlein

Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT 06877

LFA-1 (CD18,CD11a) is a cell-adhesion molecule that mediates critical immunological processes. In this paper we report the discovery and characterization of (R)-5-(4-bromobenzyl)-3-(3,5-dichlorophenyl)-1,5-dimethylimidazolidine-2,4-dione (BIRT 377), an orally bioavailable small molecule that interacts specifically with LFA-1 via noncovalent binding to the CD11a chain and prevents LFA-1 from binding to its ligand, ICAM-1. BIRT 377 inhibits lymphocyte activity both in vitro and in vivo, in functional assays that require LFA-1-mediated cell adhesion. These results demonstrate that LFA-1-mediated leukocyte adhesion can be antagonized with noncharged, low m.w. molecules and suggest that the potential therapeutic value of adhesion inhibitors can be attained with a small, orally bioavailable compound.




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