Oral Curcumin (Meriva) Is Effective as an Adjuvant Treatment and Is Able to Reduce IL-22 Serum Levels in Patients with Psoriasis Vulgaris

被引:107
作者
Antiga, Emiliano [1 ]
Bonciolini, Veronica [1 ]
Volpi, Walter [1 ]
Del Bianco, Elena [1 ]
Caproni, Marzia [1 ]
机构
[1] Univ Florence, Dept Surg & Translat Med, Dermatol Sect, I-50125 Florence, Italy
关键词
NF-KAPPA-B; EXPRESSION; ETANERCEPT; CELLS; DIFFERENTIATION; POPULATION; APOPTOSIS; AGENT; IL-17; TH17;
D O I
10.1155/2015/283634
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
Curcumin is a complementary therapy that may be helpful for the treatment of psoriasis due to its anti-inflammatory, antiangiogenic, antioxidant, and antiproliferative effects. In the present study we performed a randomized, double-blind, placebo-controlled clinical trial to assess the effectiveness of a bioavailable oral curcumin in the treatment of psoriasis. Sixty-three patients with mild-to-moderate psoriasis vulgaris (PASI < 10) were randomly divided into two groups treated with topical steroids and Meriva, a commercially available lecithin based delivery system of curcumin, at 2 g per day (arm 1), or with topical steroids alone (arm 2), both for 12 weeks. At the beginning (T0) and at the end of the therapy (T12), clinical assessment and immunoenzymatic analysis of the serum levels of IL-17 and IL-22 were performed. At T12, both groups achieved a significant reduction of PASI values that, however, was higher in patients treated with both topical steroids and oral curcumin than in patients treated only with topical steroids. Moreover, IL-22 serum levels were significantly reduced in patients treated with oral curcumin. In conclusion, curcumin was demonstrated to be effective as an adjuvant therapy for the treatment of psoriasis vulgaris and to significantly reduce serum levels of IL-22.
引用
收藏
页数:7
相关论文
共 47 条
[1]
PHARMACOLOGY OF CURCUMA-LONGA [J].
AMMON, HPT ;
WAHL, MA .
PLANTA MEDICA, 1991, 57 (01) :1-7
[2]
[Anonymous], 2013, BRIT J PHARMACOL, DOI DOI 10.1111/BPH.12131
[3]
THE ROLE OF ETANERCEPT ON THE EXPRESSION OF MARKERS OF T HELPER 17 CELLS AND THEIR PRECURSORS IN SKIN LESIONS OF PATIENTS WITH PSORIASIS VULGARIS [J].
Antiga, E. ;
Volpi, W. ;
Chiarini, C. ;
Cardilicchia, E. ;
Fili, L. ;
Manuelli, C. ;
Parronchi, P. ;
Fabbri, P. ;
Caproni, M. .
INTERNATIONAL JOURNAL OF IMMUNOPATHOLOGY AND PHARMACOLOGY, 2010, 23 (03) :767-774
[4]
Etanercept Downregulates the Th17 Pathway and Decreases the IL-17+/IL-10+ Cell Ratio in Patients with Psoriasis Vulgaris [J].
Antiga, Emiliano ;
Volpi, Walter ;
Cardilicchia, Elisa ;
Maggi, Laura ;
Fili, Lucia ;
Manuelli, Cinzia ;
Parronchi, Paola ;
Fabbri, Paolo ;
Caproni, Marzia .
JOURNAL OF CLINICAL IMMUNOLOGY, 2012, 32 (06) :1221-1232
[5]
Keratinocyte proliferation, differentiation, and apoptosis-Differential mechanisms of regulation by curcumin, EGCG and apigenin [J].
Balasubramanian, Sivaprakasam ;
Eckert, Richard L. .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2007, 224 (03) :214-219
[6]
Curcumin: An Anti-Inflammatory Molecule from a Curry Spice on the Path to Cancer Treatment [J].
Basnet, Purusotam ;
Skalko-Basnet, Natasa .
MOLECULES, 2011, 16 (06) :4567-4598
[7]
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)
[8]
IL-22 inhibits epidermal differentiation and induces proinflammatory gene expression and migration of human keratinocytes [J].
Boniface, K ;
Bernard, FX ;
Garcia, M ;
Gurney, AL ;
Lecron, JC ;
Morel, F .
JOURNAL OF IMMUNOLOGY, 2005, 174 (06) :3695-3702
[9]
Serum Levels of IL-17 and IL-22 Are Reduced by Etanercept, but not by Acitretin, in Patients with Psoriasis: a Randomized-Controlled Trial [J].
Caproni, M. ;
Antiga, E. ;
Melani, L. ;
Volpi, W. ;
Del Bianco, E. ;
Fabbri, P. .
JOURNAL OF CLINICAL IMMUNOLOGY, 2009, 29 (02) :210-214
[10]
A 50% reduction in the Psoriasis Area and Severity Index (PASI 50) is a clinically significant endpoint in the assessment of psoriasis [J].
Carlin, CS ;
Feldman, SR ;
Krueger, JG ;
Menter, A ;
Krueger, GG .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 2004, 50 (06) :859-866