Targeting the IL-23/IL-17 axis for the treatment of psoriasis and psoriatic arthritis

被引:41
作者
Alunno, Alessia [1 ]
Carubbi, Francesco [2 ]
Cafaro, Giacomo [1 ]
Pucci, Giacomo [1 ,3 ]
Battista, Francesca [1 ,3 ]
Bartoloni, Elena [1 ]
Giacomelli, Roberto [2 ]
Schillaci, Giuseppe [1 ,3 ]
Gerli, Roberto [1 ]
机构
[1] Univ Perugia, Dept Med, I-06100 Perugia, Italy
[2] Univ Aquila, Rheumatol Unit, Dept Biotechnol & Appl Clin Sci, I-67100 Laquila, Italy
[3] Terni Univ Hosp, Unit Internal Med, Terni, Italy
关键词
IL-17; IL-23; psoriasis; psoriatic arthritis; COLLAGEN-INDUCED ARTHRITIS; TO-SEVERE PSORIASIS; INTERLEUKIN-12/23; MONOCLONAL-ANTIBODY; CHRONIC PLAQUE PSORIASIS; HYPER-IGE SYNDROME; DOUBLE-BLIND; TH17; CELLS; EPIDERMAL HYPERPLASIA; RHEUMATOID-ARTHRITIS; FUNCTIONAL-ROLE;
D O I
10.1517/14712598.2015.1084284
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Introduction: A growing amount of data supporting the pathogenic role of the IL-23/IL-17 axis in inflammatory/autoimmune disorders has provided the rationale to target the system for therapeutic purpose. Several compounds have been and are currently under intense investigation in psoriasis and psoriatic arthritis (PsA) yielding impressive results.Areas covered: In this review article, we provide an overview of currently available data on the IL-23/IL-17 system as a target for treatment for psoriasis and PsA. We searched MEDLINE for articles on drug therapy for psoriasis and PsA published between 1 January 2010 and 31 May 2015. One of these agents, ustekinumab, has been recently approved for the treatment of psoriasis and PsA, and a number of IL-23/IL-17-targeted compounds under investigation in these diseases.Expert opinion: As our knowledge of the role of the IL-23/IL-17 axis in the pathogenesis of psoriasis and PsA deepens, it enables the development of more targeted therapies in the management of these conditions. Early data on IL-23/IL-17 targeting drugs appear promising, although incomplete. Given the key role IL-23/IL-17 in host defence, the safety profile of targeted drugs should be thoroughly assessed in future studies.
引用
收藏
页码:1727 / 1737
页数:11
相关论文
共 74 条
[1]
Interleukin-23 promotes a distinct CD4 T cell activation state characterized by the production of interleukin-17 [J].
Aggarwal, S ;
Ghilardi, N ;
Xie, MH ;
de Sauvage, FJ ;
Gurney, AL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (03) :1910-1914
[2]
[Anonymous], ARTHRITIS RHEUMA S10
[3]
KINETICS AND REGULATION OF HUMAN KERATINOCYTE STEM-CELL GROWTH IN SHORT-TERM PRIMARY EX-VIVO CULTURE - COOPERATIVE GROWTH-FACTORS FROM PSORIATIC LESIONAL T-LYMPHOCYTES STIMULATE PROLIFERATION AMONG PSORIATIC UNINVOLVED, BUT NOT NORMAL, STEM KERATINOCYTES [J].
BATACSORGO, Z ;
HAMMERBERG, C ;
VOORHEES, JJ ;
COOPER, KD .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (01) :317-327
[4]
Th17 and Th22 cells in psoriatic arthritis and psoriasis [J].
Benham, Helen ;
Norris, Paul ;
Goodall, Jane ;
Wechalekar, Mihir D. ;
FitzGerald, Oliver ;
Szentpetery, Agnes ;
Smith, Malcolm ;
Thomas, Ranjeny ;
Gaston, Hill .
ARTHRITIS RESEARCH & THERAPY, 2013, 15 (05)
[5]
Reduction of joint inflammation and bone erosion in rat adjuvant arthritis by treatment with interleukin-17 receptor IgG1 Fc fusion protein [J].
Bush, KA ;
Farmer, KA ;
Walker, JS ;
Kirkham, BW .
ARTHRITIS AND RHEUMATISM, 2002, 46 (03) :802-805
[6]
Involvement of interleukin-21 in the epidermal hyperplasia of psoriasis [J].
Caruso, Roberta ;
Botti, Elisabetta ;
Sarra, Massimiliano ;
Esposito, Maria ;
Stolfi, Carmine ;
Diluvio, Laura ;
Giustizieri, Maria Laura ;
Pacciani, Valentina ;
Mazzotta, Annamaria ;
Campione, Elena ;
MacDonald, Thomas T. ;
Chimenti, Sergio ;
Pallone, Francesco ;
Costanzo, Antonio ;
Monteleone, Giovanni .
NATURE MEDICINE, 2009, 15 (09) :1013-1015
[7]
Contribution of interleukin 17 to synovium matrix destruction in rheumatoid arthritis [J].
Chabaud, M ;
Garnero, P ;
Dayer, JM ;
Guerne, PA ;
Fossiez, F ;
Miossec, P .
CYTOKINE, 2000, 12 (07) :1092-1099
[8]
IL-23 stimulates epidermal hyperplasia via TNF and IL-20R2-dependent mechanisms with implications for psoriasis pathogenesis [J].
Chan, Jason R. ;
Blumenschein, Wendy ;
Murphy, Erin ;
Diveu, Caroline ;
Wiekowski, Maria ;
Abbondanzo, Susan ;
Lucian, Linda ;
Geissler, Richard ;
Brodie, Scott ;
Kimball, Alexa B. ;
Gorman, Daniel M. ;
Smith, Kathleen ;
Malefyt, Rene de Waal ;
Kastelein, Robert A. ;
McClanahan, Terrill K. ;
Bowman, Edward P. .
JOURNAL OF EXPERIMENTAL MEDICINE, 2006, 203 (12) :2577-2587
[9]
Pharmacologic Repression of Retinoic Acid Receptor-Related Orphan Nuclear Receptor γ Is Therapeutic in the Collagen-Induced Arthritis Experimental Model [J].
Chang, Mi Ra ;
Lyda, Brent ;
Kamenecka, Theodore M. ;
Griffin, Patrick R. .
ARTHRITIS & RHEUMATOLOGY, 2014, 66 (03) :579-588
[10]
Integrative Responses to IL-17 and TNF-α in Human Keratinocytes Account for Key Inflammatory Pathogenic Circuits in Psoriasis [J].
Chiricozzi, Andrea ;
Guttman-Yassky, Emma ;
Suarez-Farinas, Mayte ;
Nograles, Kristine E. ;
Tian, Suyan ;
Cardinale, Irma ;
Chimenti, Sergio ;
Krueger, James G. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2011, 131 (03) :677-687