Serum cytokine and chemokine profiles in patients with alopecia areata

被引:27
作者
Bilgic, O. [1 ]
Sivrikaya, A. [2 ]
Unlu, A. [2 ]
Altinyazar, H. C. [1 ]
机构
[1] Selcuk Univ, Sch Med, Dept Dermatol, TR-42075 Konya, Turkey
[2] Selcuk Univ, Sch Med, Dept Biochem, TR-42075 Konya, Turkey
关键词
alopecia areata; proinflammatory markers; Cytokines; chemokines; EXPRESSION; CTACK; CELLS;
D O I
10.3109/09546634.2015.1093591
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Most evidence supports the role of altered T cell-mediated immunity in the pathogenesis of alopecia areata (AA). Tough cytokines and chemokines play an important role in the immune process of AA, their expressions have been examined in limited studies. Objective: To determine serum cytokine levels of TNF-alpha, IL-6, and IL-23, and some of the Th1-(CXCL9), Th2-(CCL17), and Th17-associated (CCL20 and CCL27) chemokines in patients with AA. Methods: Forty patients with AA and 40 healthy controls were enrolled in the study. Serum concentrations of cytokines and chemokines were measured using enzyme-linked immunoassay techniques. Results: The mean serum levels of TNF-alpha, IL-6, IL-23, CXCL9, CCL17, CCL20, and CCL27 in AA patients were significantly higher than in the controls. However, with logistic regression analyses, only CCL17 and CCL27 levels showed a positive relationship, and IL-23 levels showed a negative relationship, with the presence of AA. Furthermore, serum CCL27 levels were positively correlated with AA severity. Conclusion: This study suggests that CCL17 and CCL27 may have an aggravating effect, whereas IL-23 may have a protective effect for the development of AA. Additionally, serum CCL27 levels may be useful as marker of disease severity.
引用
收藏
页码:260 / 263
页数:4
相关论文
共 27 条
[1]   Th17 cells: A new paradigm for cutaneous inflammation [J].
Asarch, Adam ;
Barak, Orr ;
Loo, Daniel S. ;
Gottlieb, Alice B. .
JOURNAL OF DERMATOLOGICAL TREATMENT, 2008, 19 (05) :259-266
[2]   Investigation of interleukin-12, interleukin-17 and interleukin-23 receptor gene polymorphisms in alopecia areata [J].
Aytekin, Nesrin ;
Akcali, Cenk ;
Pehlivan, Sacide ;
Kirtak, Necmettin ;
Inaloz, Serhat .
JOURNAL OF INTERNATIONAL MEDICAL RESEARCH, 2015, 43 (04) :526-534
[3]   Serum T helper 1 cytokine levels are greater in patients with alopecia areata regardless of severity or atopy [J].
Barahmani, N. ;
Lopez, A. ;
Babu, D. ;
Hernandez, M. ;
Donley, S. E. ;
Duvic, M. .
CLINICAL AND EXPERIMENTAL DERMATOLOGY, 2010, 35 (04) :409-416
[4]   Selective expression of chemokine monokine induced by interferon-7 in alopecia areata [J].
Benoit, S ;
Toksoy, A ;
Goebeler, M ;
Gillitzer, R .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2003, 121 (04) :933-935
[5]  
Borish Larry C., 2003, Journal of Allergy and Clinical Immunology, V111, pS460
[6]   Biological therapies in rheumatic diseases [J].
Conti, F. ;
Ceccarelli, F. ;
Massaro, L. ;
Cipriano, E. ;
Di Franco, M. ;
Alessandri, C. ;
Spinelli, F. R. ;
Scrivo, R. ;
Valesini, G. .
CLINICA TERAPEUTICA, 2013, 164 (05) :E413-E428
[7]   The IL-23/Th17 Axis in the Immunopathogenesis of Psoriasis [J].
Di Cesare, Antonella ;
Di Meglio, Paola ;
Nestle, Frank O. .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2009, 129 (06) :1339-1350
[8]   Markers of systemic inflammation in psoriasis: a systematic review and meta-analysis [J].
Dowlatshahi, E. A. ;
van der Voort, E. A. M. ;
Arends, L. R. ;
Nijsten, T. .
BRITISH JOURNAL OF DERMATOLOGY, 2013, 169 (02) :266-282
[9]   Autoimmune hair loss (alopecia areata) transferred by T lymphocytes to human scalp explants on SCID mice [J].
Gilhar, A ;
Ullmann, Y ;
Berkutzki, T ;
Assy, B ;
Kalish, RS .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (01) :62-67
[10]   A chronic contact eczema impedes migration of antigen-presenting cells in alopecia areata [J].
Gupta, Pooja ;
Freyschmidt-Paul, Pia ;
Vitacolonna, Mario ;
Kiessling, Sabine ;
Hummel, Susanne ;
Hildebrand, Dagmar ;
Marhaba, Rachid ;
Zoeller, Margot .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2006, 126 (07) :1559-1573