Allosteric inhibition of macrophage migration inhibitory factor revealed by ibudilast

Y Cho, GV Crichlow, JJ Vermeire… - Proceedings of the …, 2010 - National Acad Sciences
Y Cho, GV Crichlow, JJ Vermeire, L Leng, X Du, ME Hodsdon, R Bucala, M Cappello
Proceedings of the National Academy of Sciences, 2010National Acad Sciences
AV411 (ibudilast; 3-isobutyryl-2-isopropylpyrazolo-[1, 5-a] pyridine) is an antiinflammatory
drug that was initially developed for the treatment of bronchial asthma but which also has
been used for cerebrovascular and ocular indications. It is a nonselective inhibitor of various
phosphodiesterases (PDEs) and has varied antiinflammatory activity. More recently, AV411
has been studied as a possible therapeutic for the treatment of neuropathic pain and opioid
withdrawal through its actions on glial cells. As described herein, the PDE inhibitor AV411 …
AV411 (ibudilast; 3-isobutyryl-2-isopropylpyrazolo-[1,5-a]pyridine) is an antiinflammatory drug that was initially developed for the treatment of bronchial asthma but which also has been used for cerebrovascular and ocular indications. It is a nonselective inhibitor of various phosphodiesterases (PDEs) and has varied antiinflammatory activity. More recently, AV411 has been studied as a possible therapeutic for the treatment of neuropathic pain and opioid withdrawal through its actions on glial cells. As described herein, the PDE inhibitor AV411 and its PDE-inhibition-compromised analog AV1013 inhibit the catalytic and chemotactic functions of the proinflammatory protein, macrophage migration inhibitory factor (MIF). Enzymatic analysis indicates that these compounds are noncompetitive inhibitors of the p-hydroxyphenylpyruvate (HPP) tautomerase activity of MIF and an allosteric binding site of AV411 and AV1013 is detected by NMR. The allosteric inhibition mechanism is further elucidated by X-ray crystallography based on the MIF/AV1013 binary and MIF/AV1013/HPP ternary complexes. In addition, our antibody experiments directed against MIF receptors indicate that CXCR2 is the major receptor for MIF-mediated chemotaxis of peripheral blood mononuclear cells.
National Acad Sciences
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