High mobility group box- 1 levels may be associated with disease activity of Behcet’s disease

High mobility group box- 1 levels may be associated with disease activity of Behcet’s disease

Background/aim: High mobility group box- 1 (HMGB- 1) is a nuclear protein acting as a proinflammatory molecule. The serum HMGB- 1 levels were found elevated in chronic inflammatory diseases. In this cross-sectional study, serum HMGB- 1 levels in Behcet’s disease (BD) patients and healthy controls (HC) were studied. Also, its association with disease activity scores and clinical findings were evaluated. Materials and methods: Ninety BD patients and 50 age-sex matched HC were included in the study. Disease activity scores were assessed by Behcet Disease Current Activity Form (BDCAF) and Behcet Syndrome Activity Score (BSAS). Serum HMGB- 1 levels were measured using a commercial ELISA kit. A p value of < 0.05 was considered to be statistically significant. Results: Serum HMGB- 1 levels were significantly higher in BD than in HC (43.26 pg/mL and 16.73 pg/mL; p < 0.001, respectively). Serum HMGB- 1 levels were statistically significantly associated with presence of erythema nodosum (EN) and genital ulcers in the last one month prior to recruitment (p = 0.041 and p < 0.001, respectively). BDCAF and BSAS scores were positively correlated with serum HMGB- 1 level ( p = 0.03 and p = 0.02, respectively). Conclusion: HMGB - 1 may play a role in the development of BD. Also, due to its positive correlation with disease activity indices, it can be used as a novel disease activity parameter in BD. Key words: High mobility group box- 1, autoimmune diseases, Behcet’s disease, inflammation

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  • 1. Davatchi F. Behçet’s disease. International journal of rheumatic diseases 2018; 21 (12): 2057. doi: 10.1111/1756-185X.13465
  • 2. de Chambrun MP, Wechsler B, Geri G, Cacoub P, Saadoun D. New insights into the pathogenesis of Behcet’s disease. Autoimmunity reviews 2012; 11 (10): 687-98. doi: 10.1016/j. autrev.2011.11.026
  • 3. Lee S, Kwak MS, Kim S, Shin J-S. The role of high mobility group box 1 in innate immunity. Yonsei medical journal 2014; 55 (5): 1165-76. doi: 10.3349/ymj.2014.55.5.1165
  • 4. Pilzweger C, Holdenrieder S. Circulating HMGB1 and RAGE as clinical biomarkers in malignant and autoimmune diseases. Diagnostics 2015; 5 (2): 219-53. doi: 10.3390/ diagnostics5020219
  • 5. Huttunen HJ, Fages C, Kuja-Panula J, Ridley AJ, Rauvala H. Receptor for advanced glycation end products-binding COOH-terminal motif of amphoterin inhibits invasive migration and metastasis. Cancer research 2002; 62 (16): 4805- 11. doi: Published August 2002
  • 6. Park JS, Svetkauskaite D, He Q, Kim JY, Strassheim D et al. Involvement of toll-like receptors 2 and 4 in cellular activation by high mobility group box 1 protein. The Journal of biological chemistry 2004; 279 (9): 7370-7. doi: 10.1074/jbc.M306793200
  • 7. Park JS, Gamboni-Robertson F, He Q, Svetkauskaite D, Kim JY et al. High mobility group box 1 protein interacts with multiple Toll-like receptors. American journal of physiology Cell physiology 2006; 290 (3): C917-24. doi: 10.1152/ ajpcell.00401.2005
  • 8. Ivanov S, Dragoi AM, Wang X, Dallacosta C, Louten J et al. A novel role for HMGB1 in TLR9-mediated inflammatory responses to CpG-DNA. Blood 2007; 110 (6): 1970-81. doi: 10.1182/blood-2006-09-044776
  • 9. Kang R, Chen R, Zhang Q, Hou W, Wu S et al. HMGB1 in health and disease. Molecular aspects of medicine 2014; 40: 1-116. doi: 10.1016/j.mam.2014.05.001
  • 10. Andersson U, Wang H, Palmblad K, Aveberger A-C, Bloom O et al. High mobility group 1 protein (HMG-1) stimulates proinflammatory cytokine synthesis in human monocytes. Journal of Experimental Medicine 2000; 192 (4): 565-70. doi: 10.1084/jem.192.4.565
  • 11. Hamada T, Torikai M, Kuwazuru A, Tanaka M, Horai N et al. Extracellular high mobility group box chromosomal protein 1 is a coupling factor for hypoxia and inflammation in arthritis. Arthritis & Rheumatism 2008; 58 (9): 2675-85. doi: 10.1002/ art.23729
  • 12. Ma C-y, Jiao Y-l, Zhang J, Yang Q-r, Zhang Z-f et al. Elevated plasma level of HMGB1 is associated with disease activity and combined alterations with IFN-alpha and TNF-alpha in systemic lupus erythematosus. Rheumatology international 2012; 32 (2): 395-402. doi: 10.1007/s00296-010-1636-6
  • 13. Ulfgren AK, Grundtman C, Borg K, Alexanderson H, Andersson U et al. Down-regulation of the aberrant expression of the inflammation mediator high mobility group box chromosomal protein 1 in muscle tissue of patients with polymyositis and dermatomyositis treated with corticosteroids. Arthritis & Rheumatism 2004; 50 (5): 1586-94. doi: 10.1002/ art.20220
  • 14. Mendoza-Pinto C, García-Carrasco M, Jiménez-Hernández M, Hernández CJ, Riebeling-Navarro C et al. Etiopathogenesis of Behcet’s disease. Autoimmunity reviews 2010; 9 (4): 241-5. doi: 10.1016/j.autrev.2009.10.005
  • 15. Ling E, Shubinsky G, Press J. Increased proportion of CD3+ CD4− CD8− double-negative T cells in peripheral blood of children with Behcet’s disease. Autoimmunity reviews 2007; 6 (4): 237-40. doi: 10.1016/j.autrev.2006.08.008
  • 16. Emmi G, Bettiol A, Silvestri E, Di Scala G, Becatti M et al. Vascular Behçet’s syndrome: an update. Internal and Emergency Medicine 2019; 14 (5): 645-52. doi: 10.1007/ s11739-018-1991-y
  • 17. Dumitriu IE, Baruah P, Manfredi AA, Bianchi ME, RovereQuerini P. HMGB1: guiding immunity from within. Trends in immunology 2005; 26 (7): 381-7. doi: 10.1016/j.it.2005.04.009
  • 18. Park JS, Arcaroli J, Yum H-K, Yang H, Wang H et al. Activation of gene expression in human neutrophils by high mobility group box 1 protein. American Journal of Physiology-Cell Physiology 2003; 284 (4): C870-C9. doi: 10.1152/ajpcell.00322.2002
  • 19. ISGfBs D. Criteria for diagnosis of Behçet’s disease. International Study Group for Behcet’s Disease. Lancet 1990; 335: 1078-80.
  • 20. Alpsoy E. Behcet’s disease: a comprehensive review with a focus on epidemiology, etiology and clinical features, and management of mucocutaneous lesions. The Journal of dermatology 2016; 43 (6): 620-32. doi: 10.1111/1346- 8138.13381
  • 21. Boyvat A, Heper AO, Koçyiğit P, Erekul S, Gürgey E. Can specific vessel-based papulopustular lesions of Behçet’s disease be differentiated from nonspecific follicular-based lesions clinically? International journal of dermatology 2006; 45 (7): 814-8. doi: 10.1111/j.1365-4632.2006.02797.x
  • 22. Türsen Ü. Behçet Hastalığında Aktivite Belirteçleri. Archives of the Turkish Dermatology & Venerology/Turkderm 2009; 43.
  • 23. Yilmaz S, Simsek I, Cinar M, Erdem H, Kose O et al. Patientdriven assessment of disease activity in Behcet’s syndrome: cross-cultural adaptation, reliability and validity of the Turkish version of the Behcet’s Syndrome Activity Score. Clin Exp Rheumatol 2013; 31 (3 Suppl 77): 77-83.
  • 24. de Souza AW, Félix Perazzio S, de França NR, Andrade LEC, Bijl M et al. High mobility group box 1 serum levels are increased in Behcet’s disease, but not associated with disease activity or disease manifestations. Rheumatology 2015; 54 (12): 2151-5. doi: 10.1093/rheumatology/kev202
  • 25. Ha YJ, Park JS, Kang Mi, Lee SK, Park YB et al. Increased serum interleukin-32 levels in patients with Behçet’s disease. International journal of rheumatic diseases 2018; 21 (12): 2167-74. doi: 10.1111/1756-185X.13072
  • 26. Magna M, Pisetsky DS. The role of HMGB1 in the pathogenesis of inflammatory and autoimmune diseases. Molecular medicine 2014; 20 (1): 138-46. doi: 10.2119/molmed.2013.00164
  • 27. Harris HE, Andersson U, Pisetsky DS. HMGB1: a multifunctional alarmin driving autoimmune and inflammatory disease. Nature Reviews Rheumatology 2012; 8 (4): 195. doi: 10.1038/nrrheum.2011.222
  • 28. Andersson U, Harris HE. The role of HMGB1 in the pathogenesis of rheumatic disease. Biochimica et Biophysica Acta (BBA)-Gene Regulatory Mechanisms 2010; 1799 (1-2): 141-8. doi: 10.1016/j.bbagrm.2009.11.003
  • 29. Goldstein RS, Bruchfeld A, Yang L, Qureshi AR, GallowitschPuerta M et al. Cholinergic anti-inflammatory pathway activity and High Mobility Group Box-1 (HMGB1) serum levels in patients with rheumatoid arthritis. Molecular medicine 2007; 13 (3-4): 210-5. doi: 10.2119/2006–00108.Goldstein
  • 30. Dupire G, Nicaise C, Gangji V, Soyfoo MS. Increased serum levels of high-mobility group box 1 (HMGB1) in primary Sjögren’s syndrome. Scandinavian journal of rheumatology 2012; 41 (2): 120-3. doi: 10.3109/03009742.2011.633099
  • 31. Wang C, Miao Y, Wu X, Huang Y, Sun M et al. Serum HMGB1 serves as a novel laboratory indicator reflecting disease activity and treatment response in ankylosing spondylitis patients. Journal of immunology research 2016; 2016. doi: 10.1155/2016/6537248
  • 32. Taniguchi N, Kawahara KI, Yone K, Hashiguchi T, Yamakuchi M et al. High mobility group box chromosomal protein 1 plays a role in the pathogenesis of rheumatoid arthritis as a novel cytokine. Arthritis & Rheumatism: Official Journal of the American College of Rheumatology 2003; 48 (4): 971-81. doi: 10.1002/art.10859
  • 33. Henes F, Chen Y, Bley T, Fabel M, Both M et al. Correlation of serum level of high mobility group box 1 with the burden of granulomatous inflammation in granulomatosis with polyangiitis (Wegener’s). Annals of the rheumatic diseases 2011; 70 (11): 1926-9. doi: 10.1136/ard.2010.146456
  • 34. Ahn JK, Cha H-S, Bae E-K, Lee J, Koh E-M. Extracellular highmobility group box 1 is increased in patients with Behcet’s disease with intestinal involvement. Journal of Korean medical science 2011; 26 (5): 697-700. doi: 10.3346/jkms.2011.26.5.697
  • 35. De Martinis M, Sirufo MM, Ginaldi L. Osteoporosis: Current and emerging therapies targeted to immunological checkpoints. Current medicinal chemistry 2019. doi: 10.2174 /0929867326666190730113123
  • 36. De Martinis M, Ginaldi L, Sirufo MM, Pioggia G, Calapai G et al. Alarmins in Osteoporosis, RAGE, IL-1, and IL-33 Pathways: A Literature Review. Medicina 2020; 56 (3): 138. doi: 10.3390/ medicina56030138
  • 37. Chavakis T, Bierhaus A, Al-Fakhri N, Schneider D, Witte S et al. The pattern recognition receptor (RAGE) is a counterreceptor for leukocyte Integrins a novel pathway for inflammatory cell recruitment. The Journal of experimental medicine 2003; 198 (10): 1507-15. doi: 10.1084/jem.20030800
  • 38. Demirkesen C, Tüzüner N, Mat C, Senocak M, Büyükbabani N et al. Clinicopathologic evaluation of nodular cutaneous lesions of Behçet syndrome. American journal of clinical pathology 2001; 116 (3): 341-6. doi: 10.1309/GCTH-0060-55K8-XCTT
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