Rilonacept for the treatment of cryopyrin-associated periodic syndromes (CAPS)

被引:2
作者
Hoffman, Hal M. [1 ]
机构
[1] Univ Calif San Diego, Div Rheumatol Allergy & Immunol, La Jolla, CA 92093 USA
关键词
cryopyrin-associated periodic syndromes; IL-1; Trap; interleukin-1; rilonacept; COLD AUTOINFLAMMATORY SYNDROME; INTERLEUKIN-1 RECEPTOR ANTAGONIST; RHEUMATOID-ARTHRITIS; CIAS1; MUTATIONS; DOUBLE-BLIND; GENE; INFLAMMASOME; ANAKINRA; IL-1; MULTICENTER;
D O I
10.1517/14712590902875518
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 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Cryopyrin-associated periodic syndromes (CAPS) encompass a group of rare inherited, autoinflammatory disorders that represent a spectrum of one disease with varying degrees of severity. Until recently, there was no effective treatment for CAPS, but identification of the genetic basis of CAPS highlighted the pathogenic role of IL-1 beta. Objectives: Rilonacept is a recently FDA approved biologic therapy for CAPS with high affinity for IL-1 beta. Limited pharmacological data has been reported to date. Methods: A review of the phamacokinetics and pharmacodynamics data as well as the results of a pilot study and Phase III placebo-controlled trials of rilonacept in CAPS. Unpublished data on an open-label extension study in adult and pediatric subjects is also reviewed. Results: Rilonacept produced rapid and profound improvements in symptoms and also reduced high-sesitivity C-reactive protein levels and normalized elevated serum amyloid A concentrations, an important risk factor for amyloidosis. The primary adverse events were injection-site reactions and upper respiratory tract infections. Conclusion: Rilonacept, the only IL-1 Trap, is the first of many novel IL-1-targeted therapies being developed. in a very short time it has changed the lives of CAPS patients.
引用
收藏
页码:519 / 531
页数:13
相关论文
共 49 条
[1]   Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis [J].
Aganna, E ;
Martinon, F ;
Hawkins, PN ;
Ross, JB ;
Swan, DC ;
Booth, DR ;
Lachmann, HJ ;
Gaudet, R ;
Woo, P ;
Feighery, C ;
Cotter, FE ;
Thome, M ;
Hitman, GA ;
Tschopp, J ;
McDermott, MF .
ARTHRITIS AND RHEUMATISM, 2002, 46 (09) :2445-2452
[2]   NALP3 forms an IL-lβ-Processing inflammasome with increased activity in Muckle-Wells autoinflammatory disorder [J].
Agostini, L ;
Martinon, F ;
Burns, K ;
McDermott, MF ;
Hawkins, PN ;
Tschopp, J .
IMMUNITY, 2004, 20 (03) :319-325
[3]   De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID) -: A new member of the expanding family of pyrin-associated autoinflammatory diseases [J].
Aksentijevich, I ;
Nowak, M ;
Mallah, M ;
Chae, JJ ;
Watford, WT ;
Hofmann, SR ;
Stein, L ;
Russo, R ;
Goldsmith, D ;
Dent, P ;
Rosenberg, HF ;
Austin, F ;
Remmers, EF ;
Balow, JE ;
Rosenzweig, S ;
Komarow, H ;
Shoham, NG ;
Wood, G ;
Jones, J ;
Mangra, N ;
Carrero, H ;
Adams, BS ;
Moore, TL ;
Schikler, K ;
Hoffman, H ;
Lovell, DJ ;
Lipnick, R ;
Barron, K ;
O'Shea, JJ ;
Kastner, DL ;
Goldbach-Mansky, R .
ARTHRITIS AND RHEUMATISM, 2002, 46 (12) :3340-3348
[4]   The clinical continuum of cryopyrinopathies -: Novel CIAS1 mutations in north American patients and a new cryopyrin model [J].
Aksentijevich, Ivona ;
Putnam, Christopher D. ;
Remmers, Elaine F. ;
Mueller, James L. ;
Le, Julie ;
Kolodner, Richard D. ;
Moak, Zachary ;
Chuang, Michael ;
Austin, Frances ;
Goldbach-Mansky, Raphaela ;
Hoffman, Hal M. ;
Kastner, Daniel L. .
ARTHRITIS AND RHEUMATISM, 2007, 56 (04) :1273-1285
[5]   Neonatal-onset multisystem inflammatory disease (NOMID) due to a novel S331R mutation of the CIAS1 gene and response to interleukin-1 receptor antagonist treatment [J].
Boschan, C ;
Witt, O ;
Lohse, P ;
Foeldvari, I ;
Zappel, H ;
Schweigerer, L .
AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2006, 140A (08) :883-886
[6]   The expanding interleukin-1 family and its receptors - Do alternative IL-1 receptor/signaling pathways exist in the brain? [J].
Boutin, H ;
Kimber, I ;
Rothwell, NJ ;
Pinteaux, E .
MOLECULAR NEUROBIOLOGY, 2003, 27 (03) :239-248
[7]   Therapeutic potential of targeting IL-1 and IL-18 in inflammation [J].
Braddock, M ;
Quinn, A ;
Canvin, J .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2004, 4 (06) :847-860
[8]  
Bresnihan B, 1998, ARTHRITIS RHEUM, V41, P2196, DOI 10.1002/1529-0131(199812)41:12<2196::AID-ART15>3.3.CO
[9]  
2-U
[10]   Is IL-I a good therapeutic target in the treatment of arthritis? [J].
Burger, Danielle ;
Dayer, Jean-Michel ;
Palmer, Gaby ;
Gabay, Cem .
BEST PRACTICE & RESEARCH IN CLINICAL RHEUMATOLOGY, 2006, 20 (05) :879-896