Dipeptidyl peptidase inhibitors, an emerging drug class for inflammatory disease?

被引:212
作者
Yazbeck, Roger [1 ,2 ]
Howarth, Gordon S. [1 ,2 ,3 ]
Abbott, Catherine A. [1 ]
机构
[1] Flinders Univ S Australia, Sch Biol Sci, Adelaide, SA 5001, Australia
[2] Womens & Childrens Hosp, Ctr Paediat & Adolescent Gastroenterol, Adelaide, SA, Australia
[3] Univ Adelaide, Sch Agr Food & Wine, Discipline Agr & Anim Sci, Adelaide, SA 5005, Australia
关键词
GLUCAGON-LIKE PEPTIDE-2; T-CELL-ACTIVATION; IV DP-IV; CIRCULATING LEVELS; INSULIN-SECRETION; AMINOPEPTIDASE-N; DPP-4; INHIBITOR; CD26; EXPRESSION; ENZYMES;
D O I
10.1016/j.tips.2009.08.003
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Dipeptidyl peptidase (DPP)-4 is a member of the S9b serine protease family, which also includes DPP8 and DPP9. DPP4 cleaves a number of regulatory factors, including chemokines and growth factors. DPP4 inhibitors have recently emerged as an effective treatment option for type 2 diabetes. Early in vitro studies demonstrated that DPP4 inhibitors inhibit T-cell proliferation and cytokine production, leading to their investigation in numerous pre-clinical models of inflammatory diseases, including arthritis, multiple sclerosis and inflammatory bowel disease. Recent data suggest that the early DPP4-specific inhibitors might also bind DPP8 and DPP9, thus exerting their effects through non-specific binding. This review highlights recent insights into the applicability of DPP inhibitors as novel pharmacological agents for inflammatory disease.
引用
收藏
页码:600 / 607
页数:8
相关论文
共 72 条
[1]   Cloning, expression and chromosomal localization of a novel human dipeptidyl peptidase (DPP) IV homolog, DPP8 [J].
Abbott, CA ;
Yu, DMT ;
Woollatt, E ;
Sutherland, GR ;
McCaughan, GW ;
Gorrell, MD .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (20) :6140-6150
[2]   Two highly conserved glutamic acid residues in the predicted β propeller domain of dipeptidyl peptidase IV are required for its enzyme activity [J].
Abbott, CA ;
McCaughan, GW ;
Gorrell, MD .
FEBS LETTERS, 1999, 458 (03) :278-284
[3]   Inhibition of dipeptidyl peptidase-4 augments insulin secretion in response to exogenously administered glucagon-like peptide-1, glucose-dependent insulinotropic polypeptide, pituitary adenylate cyclase-activating polypeptide, and gastrin-releasing peptide in mice [J].
Ahrén, B ;
Hughes, TE .
ENDOCRINOLOGY, 2005, 146 (04) :2055-2059
[4]   Twelve- and 52-week efficacy of the dipeptidyl peptidase IV inhibitor LAF237 in metformin-treated patients with type 2 diabetes [J].
Ahrén, B ;
Gomis, R ;
Standl, E ;
Mills, D ;
Schweizer, A .
DIABETES CARE, 2004, 27 (12) :2874-2880
[5]   DPP-4 inhibitors [J].
Ahren, Bo .
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM, 2007, 21 (04) :517-533
[6]   Dipeptidyl peptidase 9 has two forms, a broad tissue distribution, cytoplasmic localization and DPIV-like peptidase activity [J].
Ajami, K ;
Abbott, CA ;
McCaughan, GW ;
Gorrell, MD .
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION, 2004, 1679 (01) :18-28
[7]   Stromal cell-derived factors 1α and 1β, inflammatory protein-10 and interferon-inducible T cell chemo-attractant are novel substrates of dipeptidyl peptidase 8 [J].
Ajami, Katerina ;
Pitman, Melissa R. ;
Wilson, Claire H. ;
Park, Joohong ;
Menz, R. Ian ;
Starr, Amanda E. ;
Cox, Jennifer H. ;
Abbott, Catherine A. ;
Overall, Christopher M. ;
Gorrell, Mark D. .
FEBS LETTERS, 2008, 582 (05) :819-825
[8]   Efficacy and safety of incretin therapy in type 2 diabetes - Systematic review and meta-analysis [J].
Amori, Renee E. ;
Lau, Joseph ;
Pittas, Anastassios G. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2007, 298 (02) :194-206
[9]   Biology of incretins: GLP-1 and GIP [J].
Baggio, Laurie L. ;
Drucker, Daniel J. .
GASTROENTEROLOGY, 2007, 132 (06) :2131-2157
[10]   Inflammatory bowel diseases:: multiple benefits from therapy with dipeptidyl- and alanyl-aminopeptidase inhibitors [J].
Bank, Ute ;
Bohr, Ulrich R. M. ;
Reinhold, Dirk ;
Lendeckel, Uwe ;
Ansorge, Siegfried ;
Malfertheiner, Peter ;
Taeger, Michael .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2008, 13 :3699-3713