Inhibition of interleukin-17, interleukin-23 and the TH17 cell pathway in the treatment of psoriatic arthritis and psoriasis

被引:155
作者
Mease, Philip J. [1 ,2 ]
机构
[1] Swedish Med Ctr, Seattle, WA USA
[2] Univ Washington, Sch Med, Seattle, WA USA
关键词
biologics; interleukin-17; interleukin-23; psoriasis; psoriatic arthritis; PLACEBO-CONTROLLED TRIAL; ANTI-INTERLEUKIN-17; MONOCLONAL-ANTIBODY; SIGNIFICANTLY IMPROVES SIGNS; DOUBLE-BLIND; RHEUMATOID-ARTHRITIS; PLAQUE PSORIASIS; PHASE-II; SECUKINUMAB; USTEKINUMAB; SAFETY;
D O I
10.1097/BOR.0000000000000147
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose of review In recent years, there has been an increasing understanding of the importance of the TH17 lineage of T cells and related cytokines, including interleukin (IL) 17 and IL23, not only in the biology of innate host defense but also in the pathogenesis of inflammatory/autoimmune diseases. These diseases include psoriasis, psoriatic arthritis, the broader category of spondyloarthritides including ankylosing spondylitis and rheumatoid arthritis. It is postulated that in genetically predisposed individuals, external or internal stimuli such as microbial antigens, alterations in the intestinal microbiome, biomechanical stress and/or immunologic dysregulation may lead to an increased expression of cytokines such as IL23, which in turn stimulate the differentiation and activation of TH17 and other immune cells, which are a part of the innate immune system that trigger adaptive immune processes and chronic inflammatory diseases. Herein, we explore the effect of targeting this pathway therapeutically. Recent findings New drugs that are designed to inhibit steps in this pathway, the IL12/IL23 inhibitor, ustekinumab, the IL17A inhibitors secukinumab and ixekizumab, the IL17A receptor inhibitor, brodalumab, and the IL23 inhibitors guselkumab and tildrakizumab, have demonstrated significant effectiveness in treating these diseases, particularly psoriasis, psoriatic arthritis and ankylosing spondylitis. Summary This article reviews the relevant biology, efficacy and safety of new medications targeting the TH17 pathway, including inhibition of IL17 and IL23, particularly in psoriasis and psoriatic arthritis. Especially for patients who have not gained benefit from, lost effectiveness to or could not use antitumour necrosis factor (TNF) medications for safety or tolerability reasons, having effective medicines with an alternative mechanism of action will improve our ability to diminish disease activity impact on patient lives.
引用
收藏
页码:127 / 133
页数:7
相关论文
共 33 条
[1]  
Baeten DL, 2014, ARTHRITIS RHEUMATOL, V66, pS360
[2]   The Interleukin-17 Pathway in Psoriasis and Psoriatic Arthritis: Disease Pathogenesis and Possibilities of Treatment [J].
Frleta, Marina ;
Siebert, Stefan ;
McInnes, Iain B. .
CURRENT RHEUMATOLOGY REPORTS, 2014, 16 (04)
[3]   A Phase II Randomized Study of Subcutaneous Ixekizumab, an Anti-Interleukin-17 Monoclonal Antibody, in Rheumatoid Arthritis Patients Who Were Naive to Biologic Agents or Had an Inadequate Response to Tumor Necrosis Factor Inhibitors [J].
Genovese, Mark C. ;
Greenwald, Maria ;
Cho, Chul-Soo ;
Berman, Alberto ;
Jin, Ling ;
Cameron, Gregory S. ;
Benichou, Olivier ;
Xie, Li ;
Braun, Daniel ;
Berclaz, Pierre-Yves ;
Banerjee, Subhashis .
ARTHRITIS & RHEUMATOLOGY, 2014, 66 (07) :1693-1704
[4]   Efficacy and safety of secukinumab in patients with rheumatoid arthritis: a phase II, dose-finding, double-blind, randomised, placebo controlled study [J].
Genovese, Mark C. ;
Durez, Patrick ;
Richards, Hanno B. ;
Supronik, Jerzy ;
Dokoupilova, Eva ;
Mazurov, Vadim ;
Aelion, Jacob A. ;
Lee, Sang-Heon ;
Codding, Christine E. ;
Kellner, Herbert ;
Ikawa, Takashi ;
Hugot, Sophie ;
Mpofu, Shephard .
ANNALS OF THE RHEUMATIC DISEASES, 2013, 72 (06) :863-869
[5]   Increased numbers of circulating polyfunctional Th17 memory cells in patients with seronegative spondylarthritides [J].
Jandus, Camilla ;
Bioley, Gilles ;
Rivals, Jean-Paul ;
Dudler, Jean ;
Speiser, Daniel ;
Romero, Pedro .
ARTHRITIS AND RHEUMATISM, 2008, 58 (08) :2307-2317
[6]   Ustekinumab, an anti-IL-12/23 p40 monoclonal antibody, inhibits radiographic progression in patients with active psoriatic arthritis: results of an integrated analysis of radiographic data from the phase 3, multicentre, randomised, double-blind, placebo-controlled PSUMMIT-1 and PSUMMIT-2 trials [J].
Kavanaugh, Arthur ;
Ritchlin, Christopher ;
Rahman, Proton ;
Puig, Lluis ;
Gottlieb, Alice B. ;
Li, Shu ;
Wang, Yuhua ;
Noonan, Lenore ;
Brodmerkel, Carrie ;
Song, Michael ;
Mendelsohn, Alan M. ;
McInnes, Iain B. .
ANNALS OF THE RHEUMATIC DISEASES, 2014, 73 (06) :1000-1006
[7]   Secukinumab in Plaque Psoriasis - Results of Two Phase 3 Trials [J].
Langley, Richard G. ;
Elewski, Boni E. ;
Lebwohl, Mark ;
Reich, Kristian ;
Griffiths, Christopher E. M. ;
Papp, Kim ;
Puig, Lluis ;
Nakagawa, Hidemi ;
Spelman, Lynda ;
Sigurgeirsson, Bardur ;
Rivas, Enrique ;
Tsai, Tsen-Fang ;
Wasel, Norman ;
Tyring, Stephen ;
Salko, Thomas ;
Hampele, Isabelle ;
Notter, Marianne ;
Karpov, Alexander ;
Helou, Silvia ;
Papavassilis, Charis .
NEW ENGLAND JOURNAL OF MEDICINE, 2014, 371 (04) :326-338
[8]   Anti-Interleukin-17 Monoclonal Antibody Ixekizumab in Chronic Plaque Psoriasis [J].
Leonardi, Craig ;
Matheson, Robert ;
Zachariae, Claus ;
Cameron, Gregory ;
Li, Linda ;
Edson-Heredia, Emily ;
Braun, Daniel ;
Banerjee, Subhashis .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (13) :1190-1199
[9]  
Leonardi CL, 2014, SEMIN CUTAN MED SURG, V33, pS37, DOI 10.12788/j.sder.0066
[10]   Primed for inflammation: enthesis-resident T cells [J].
Lories, Rik J. ;
McInnes, Iain B. .
NATURE MEDICINE, 2012, 18 (07) :1018-1019