Inhibition of high-mobility group box 1 as therapeutic option in autoimmune disease: lessons from animal models

被引:24
作者
Schaper, Fleur [1 ]
Heeringa, Peter [2 ]
Bijl, Marc [3 ]
Westra, Johanna [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Rheumatol & Clin Immunol, Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Med Biol Sect, Dept Pathol & Med Biol, Groningen, Netherlands
[3] Martini Hosp, Dept Internal Med & Rheumatol, Groningen, Netherlands
关键词
animal models; anti-HMGB1; autoimmune diseases; HMGB1; intervention; CHROMOSOMAL-PROTEIN; 1; SYSTEMIC-LUPUS-ERYTHEMATOSUS; ISCHEMIA-REPERFUSION INJURY; RECEPTOR; HIGH-MOBILITY-GROUP-BOX-1; PROTEIN; HMGB1; TRANSLOCATION; INDUCED ARTHRITIS; CELL RECRUITMENT; CYTOKINE RELEASE; HUMAN MONOCYTES;
D O I
10.1097/BOR.0b013e32835cee2d
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Purpose of review High-mobility group box 1 (HMGB1) is a molecule that has gained much attention in the last couple of years as an important player in innate immune responses and modulating factor in several (auto) immune diseases. Furthermore, advancements have been made in identifying the diverse functions that HMGB1 can play in the body by studying its receptors, pathways and effects. This review will focus on the modulation of HMGB1 in animal models of (auto) immune diseases. Recent findings In different disease models like sepsis, ischemia-reperfusion and arthritis, HMGB1-blocking therapies have been tested and the disease course was shown to be ameliorated. Summary These findings indicate that HMGB1 is an important mediator in innate immunity, inflammation and sterile injury. Furthermore, HMGB1 might be a new therapeutic target in inflammation and autoimmune diseases, which may be translated to the clinic.
引用
收藏
页码:254 / 259
页数:6
相关论文
共 52 条
[1]
Urine levels of HMGB1 in Systemic Lupus Erythematosus patients with and without renal manifestations [J].
Abdulahad, Deena A. ;
Westra, Johanna ;
Bijzet, Johannes ;
Dolff, Sebastian ;
van Dijk, Marcory C. ;
Limburg, Pieter C. ;
Kallenberg, Cees G. M. ;
Bijl, Marc .
ARTHRITIS RESEARCH & THERAPY, 2012, 14 (04)
[2]
High mobility group box 1 (HMGB1) and anti-HMGB1 antibodies and their relation to disease characteristics in systemic lupus erythematosus [J].
Abdulahad, Deena A. ;
Westra, Johanna ;
Bijzet, Johannes ;
Limburg, Pieter C. ;
Kallenberg, Cees G. M. ;
Bijl, Marc .
ARTHRITIS RESEARCH & THERAPY, 2011, 13 (03)
[3]
Intraarticular glucocorticoid treatment reduces inflammation in synovial cell infiltrations more efficiently than in synovial blood vessels [J].
af Klint, E ;
Grundtman, C ;
Engström, M ;
Catrina, AI ;
Makrygiannakis, D ;
Klareskog, L ;
Andersson, U ;
Ulfgren, AK .
ARTHRITIS AND RHEUMATISM, 2005, 52 (12) :3880-3889
[4]
High mobility group 1 protein (HMG-1) stimulates proinflammatory cytokine synthesis in human monocytes [J].
Andersson, U ;
Wang, HC ;
Palmblad, K ;
Aveberger, AC ;
Bloom, O ;
Erlandsson-Harris, H ;
Janson, A ;
Kokkola, R ;
Zhang, MH ;
Yang, H ;
Tracey, KJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2000, 192 (04) :565-570
[5]
RETRACTED: Diet Restriction Inhibits Apoptosis and HMGB1 Oxidation and Promotes Inflammatory Cell Recruitment during Acetaminophen Hepatotoxicity (Publication with Expression of Concern. See vol. 26, 2020) (Retracted article. See vol. 26, 2020) [J].
Antoine, Daniel James ;
Williams, Dominic P. ;
Kipar, Anja ;
Laverty, Hugh ;
Park, B. Kevin .
MOLECULAR MEDICINE, 2010, 16 (11-12) :479-490
[6]
The lack of chromosomal protein Hmg1 does not disrupt cell growth but causes lethal hypoglycaemia in newborn mice [J].
Calogero, S ;
Grassi, F ;
Aguzzi, A ;
Voigtländer, T ;
Ferrier, P ;
Ferrari, S ;
Bianchi, ME .
NATURE GENETICS, 1999, 22 (03) :276-280
[7]
HMGB1 Mediates Cognitive Impairment in Sepsis Survivors [J].
Chavan, Sangeeta S. ;
Huerta, Patricio T. ;
Robbiati, Sergio ;
Valdes-Ferrer, S. I. ;
Ochani, Mahendar ;
Dancho, Meghan ;
Frankfurt, Maya ;
Volpe, Bruce T. ;
Tracey, Kevin J. ;
Diamond, Betty .
MOLECULAR MEDICINE, 2012, 18 (06) :930-937
[8]
HMGB1 in vascular diseases: Its role in vascular inflammation and atherosclerosis [J].
de Souza, A. W. S. ;
Westra, J. ;
Limburg, P. C. ;
Bijl, M. ;
Kallenberg, C. G. M. .
AUTOIMMUNITY REVIEWS, 2012, 11 (12) :909-917
[9]
Increased serum levels of high-mobility group box 1 (HMGB1) in primary Sjogren's syndrome [J].
Dupire, G. ;
Nicaise, C. ;
Gangji, V. ;
Soyfoo, M. S. .
SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 2012, 41 (02) :120-123
[10]
The persistent release of HMGB1 contributes to tactile hyperalgesia in a rodent model of neuropathic pain [J].
Feldman, Polina ;
Due, Michael R. ;
Ripsch, Matthew S. ;
Khanna, Rajesh ;
White, Fletcher A. .
JOURNAL OF NEUROINFLAMMATION, 2012, 9