The New Insight into the Role of Antimicrobial Proteins-Alarmins in the Immunopathogenesis of Psoriasis

被引:47
作者
Batycka-Baran, A. [1 ]
Maj, J. [1 ]
Wolf, R. [2 ]
Szepietowski, J. C. [1 ]
机构
[1] Wroclaw Med Univ, Dept Dermatol Venereol & Allergol, PL-50368 Wroclaw, Poland
[2] Univ Munich, Dept Dermatol & Allergol, D-80539 Munich, Germany
关键词
PLASMACYTOID DENDRITIC CELLS; PEPTIDE LL-37; CATHELICIDIN LL-37; MOLECULAR-CLONING; VITAMIN-D; GENE-EXPRESSION; ALPHA-DEFENSINS; INNATE IMMUNITY; SKIN; RECEPTOR;
D O I
10.1155/2014/628289
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The pathognesis of psoriasis still remains not fully elucidated. Recent advances favor the idea that interactions between innate and adaptive immune response drive inflammatory process in this disease. Innate antimicrobial peptides and proteins (AMPs) are diverse group of small molecules that provide the first line of defense against invading pathogens. In recent years, the novel functions ofAMPs have been identified. There are three subclasses among AMPs that have gained the special interest as a potentially important player in the pathogenesis of psoriasis: cathelicidin, S100 proteins, and defensins. These AMPs have been shown to modulate and trigger host immune response in psoriasis acting as interplayer between innate and adaptive immune mechanisms. Overexpressed in psoriatic lesions, they prime immune cells for enhanced production of proinflammatory mediators and act as chemoattractant for leukocytes. Therefore, the novel term describing AMPs alarmins has been suggested. As multifunctional player in pathogenesis of psoriasis, AMPs may constitute potential target for therapeutic interventions. However, further investigations are required to establish the methods of downregulation of the aberrant proinflammatory functions of AMPs without increasing the risk of infections.
引用
收藏
页数:10
相关论文
共 87 条
[11]   Human antimicrobial peptide LL-37 modulates proinflammatory responses induced by cytokine milieus and double-stranded RNA in human keratinocytes [J].
Chen, Xue ;
Takai, Toshiro ;
Xie, Yang ;
Niyonsaba, Francois ;
Okumura, Ko ;
Ogawa, Hideoki .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2013, 433 (04) :532-537
[12]   Antimicrobial peptides human β-defensin (hBD)-3 and hBD-4 activate mast cells and increase skin vascular permeability [J].
Chen, Xuejun ;
Niyonsaba, Francois ;
Ushio, Hiroko ;
Hara, Mutsuko ;
Yokoi, Hidenori ;
Matsumoto, Kenji ;
Saito, Hirohisa ;
Nagaoka, Isao ;
Ikeda, Shigaku ;
Okumura, Ko ;
Ogawa, Hideoki .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2007, 37 (02) :434-444
[13]   Cathelicidin LL-37: a defense molecule with a potential role in psoriasis pathogenesis [J].
Dombrowski, Yvonne ;
Schauber, Juergen .
EXPERIMENTAL DERMATOLOGY, 2012, 21 (05) :327-330
[14]   Cytosolic DNA Triggers Inflammasome Activation in Keratinocytes in Psoriatic Lesions [J].
Dombrowski, Yvonne ;
Peric, Mark ;
Koglin, Sarah ;
Kammerbauer, Claudia ;
Goess, Christine ;
Anz, David ;
Simanski, Maren ;
Glaeser, Regine ;
Harder, Juergen ;
Hornung, Veit ;
Gallo, Richard L. ;
Ruzicka, Thomas ;
Besch, Robert ;
Schauber, Juergen .
SCIENCE TRANSLATIONAL MEDICINE, 2011, 3 (82)
[15]   Intracellular and extracellular roles of s100 proteins [J].
Donato, R .
MICROSCOPY RESEARCH AND TECHNIQUE, 2003, 60 (06) :540-551
[16]   The expression of the gene coding for the antibacterial peptide LL-37 is induced in human keratinocytes during inflammatory disorders [J].
Frohm, M ;
Agerberth, B ;
Ahangari, G ;
StahleBackdahl, M ;
Liden, S ;
Wigzell, H ;
Gudmundsson, GH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (24) :15258-15263
[17]   Endogenous production of antimicrobial peptides in innate immunity and human disease [J].
Gallo, RL ;
Nizet, V .
CURRENT ALLERGY AND ASTHMA REPORTS, 2003, 3 (05) :402-409
[18]   Self-RNA-antimicrobial peptide complexes activate human dendritic cells through TLR7 and TLR8 [J].
Ganguly, Dipyaman ;
Chamilos, Georgios ;
Lande, Roberto ;
Gregorio, Josh ;
Meller, Stephan ;
Facchinetti, Valeria ;
Homey, Bernhard ;
Barrat, Franck J. ;
Zal, Tomasz ;
Gilliet, Michel .
JOURNAL OF EXPERIMENTAL MEDICINE, 2009, 206 (09) :1983-1994
[19]   Psoriasis: rationale for targeting interleukin-17 [J].
Girolomoni, G. ;
Mrowietz, U. ;
Paul, C. .
BRITISH JOURNAL OF DERMATOLOGY, 2012, 167 (04) :717-724
[20]   Human slan (6-sulfo LacNAc) dendritic cells are inflammatory dermal dendritic cells in psoriasis and drive strong TH17/TH1 T-cell responses [J].
Haensel, Anja ;
Guenther, Claudia ;
Ingwersen, Jens ;
Starke, Josephine ;
Schmitz, Marc ;
Bachmann, Michael ;
Meurer, Michael ;
Rieber, Ernst Peter ;
Schaekel, Knut .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2011, 127 (03) :787-U456