IL-6 biology: implications for clinical targeting in rheumatic disease

被引:242
作者
Calabrese, Leonard H. [1 ]
Rose-John, Stefan [2 ]
机构
[1] Case Western Reserve Univ, Lerner Coll Med, Cleveland Clin, Dept Rheumat & Immunol Dis, Cleveland, OH 44195 USA
[2] Univ Kiel, Dept Biochem, D-24098 Kiel, Germany
关键词
SOLUBLE INTERLEUKIN-6 RECEPTOR; T-CELL; INTESTINAL INFLAMMATION; EPITHELIAL-CELLS; BASIC SCIENCE; CUTTING EDGE; TOCILIZUMAB; ARTHRITIS; BLOCKADE; CYTOKINE;
D O I
10.1038/nrrheum.2014.127
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IL-6 has been linked to numerous diseases associated with inflammation, including rheumatoid arthritis, inflammatory bowel disease, vasculitis and several types of cancer. Moreover, IL-6 is important in the induction of hepatic acute-phase proteins for the trafficking of acute and chronic inflammatory cells, the differentiation of adaptive T-cell responses, and tissue regeneration and homeostatic regulation. Studies have investigated IL-6 biology using cell-bound IL-6 receptors expressed predominantly on hepatocytes and certain haematopoietic cells versus activation mediated by IL-6 and soluble IL-6 receptors via a second protein, gp130, which is expressed throughout the body. Advances in this research elucidating the differential effects of IL-6 activation provide important insights into the role of IL-6 in health and disease, as well as its potential as a therapeutic target. Knowledge of the basic biology of IL-6 and its signalling pathways can better inform both the research agenda for IL-6-based targeted therapies as well as the clinical use of strategies affecting IL-6-mediated inflammation. This Review covers novel, emerging aspects of the biology of IL-6, which might lead to more specific blockade of IL-6 signalling without compromising the protective function of this cytokine in the body's defence against infections.
引用
收藏
页码:720 / 727
页数:8
相关论文
共 92 条
[1]   Heterogeneity of human effector CD4+ T cells [J].
Annunziato, Francesco ;
Romagnani, Sergio .
ARTHRITIS RESEARCH & THERAPY, 2009, 11 (06)
[2]   Blockade of interleukin 6 trans signaling suppresses T-cell resistance against apoptosis in chronic intestinal inflammation:: Evidence in Crohn disease and experimental colitis in vivo [J].
Atreya, R ;
Mudter, J ;
Finotto, S ;
Müllberg, J ;
Jostock, T ;
Wirtz, S ;
Schütz, M ;
Bartsch, B ;
Holtmann, M ;
Becker, C ;
Strand, D ;
Czaja, J ;
Schlaak, JF ;
Lehr, HA ;
Autschbach, F ;
Schürmann, G ;
Nishimoto, N ;
Yoshizaki, K ;
Ito, H ;
Kishimoto, T ;
Galle, PR ;
Rose-John, S ;
Neurath, MF .
NATURE MEDICINE, 2000, 6 (05) :583-588
[3]   Distinct role of gp130 activation in promoting self-renewal divisions by mitogenically stimulated murine hematopoietic stem cells [J].
Audet, J ;
Miller, CL ;
Rose-John, S ;
Piret, JM ;
Eaves, CJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (04) :1757-1762
[4]   Selective blockade of interleukin-6 trans-signaling improves survival in a murine polymicrobial sepsis model [J].
Barkhausen, Tanja ;
Tschernig, Thomas ;
Rosenstiel, Philip ;
van Griensven, Martijn ;
Vonberg, Ralf-Peter ;
Dorsch, Martina ;
Mueller-Heine, Annika ;
Chalaris, Athena ;
Scheller, Juergen ;
Rose-John, Stefan ;
Seegert, Dirk ;
Krettek, Christian ;
Waetzig, Georg H. .
CRITICAL CARE MEDICINE, 2011, 39 (06) :1407-1413
[5]   TGF-β suppresses tumor progression in colon cancer by inhibition of IL-6 trans-signaling [J].
Becker, C ;
Fantini, MC ;
Schramm, C ;
Lehr, HA ;
Wirtz, S ;
Nikolaev, A ;
Burg, J ;
Strand, S ;
Kiesslich, R ;
Huber, S ;
Ito, H ;
Nishimoto, N ;
Yoshizaki, K ;
Nishimoto, N ;
Galle, PR ;
Blessing, M ;
Rose-John, S ;
Neurath, MF .
IMMUNITY, 2004, 21 (04) :491-501
[6]  
Becker C, 2005, CELL CYCLE, V4, P217
[7]   Reciprocal developmental pathways for the generation of pathogenic effector TH17 and regulatory T cells [J].
Bettelli, E ;
Carrier, YJ ;
Gao, WD ;
Korn, T ;
Strom, TB ;
Oukka, M ;
Weiner, HL ;
Kuchroo, VK .
NATURE, 2006, 441 (7090) :235-238
[8]   A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells [J].
Black, RA ;
Rauch, CT ;
Kozlosky, CJ ;
Peschon, JJ ;
Slack, JL ;
Wolfson, MF ;
Castner, BJ ;
Stocking, KL ;
Reddy, P ;
Srinivasan, S ;
Nelson, N ;
Boiani, N ;
Schooley, KA ;
Gerhart, M ;
Davis, R ;
Fitzner, JN ;
Johnson, RS ;
Paxton, RJ ;
March, CJ ;
Cerretti, DP .
NATURE, 1997, 385 (6618) :729-733
[9]   Cutting edge: Soluble IL-6R is produced by IL-6R ectodomain shedding in activated CD4 T cells [J].
Briso, Eva M. ;
Dienz, Oliver ;
Rincon, Mercedes .
JOURNAL OF IMMUNOLOGY, 2008, 180 (11) :7102-7106
[10]   Apoptosis is a natural stimulus of IL6R shedding and contributes to the proinflammatory trans-signaling function of neutrophils [J].
Chalaris, Athena ;
Rabe, Bjoern ;
Paliga, Krzysztof ;
Lange, Hans ;
Laskay, Tamas ;
Fielding, Ceri A. ;
Jones, Simon A. ;
Rose-John, Stefan ;
Scheller, Juergen .
BLOOD, 2007, 110 (06) :1748-1755