Plasma IL-6 concentration correlates with clinical disease activity and serum C-reactive protein concentration in chronic urticaria patients
Summary Background Our previous study was the first to demonstrate enhanced plasma IL‐6 concentrations in chronic urticaria (CU). It is known that C‐reactive protein (CRP) is a sensitive marker of an underlying systemic inflammation, triggered mainly as a response to IL‐6. Objective To evaluate plas...
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Published in | Clinical and experimental allergy Vol. 41; no. 10; pp. 1386 - 1391 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.10.2011
Blackwell Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 0954-7894 1365-2222 1365-2222 |
DOI | 10.1111/j.1365-2222.2011.03789.x |
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Abstract | Summary
Background Our previous study was the first to demonstrate enhanced plasma IL‐6 concentrations in chronic urticaria (CU). It is known that C‐reactive protein (CRP) is a sensitive marker of an underlying systemic inflammation, triggered mainly as a response to IL‐6.
Objective To evaluate plasma IL‐6 concentration in CU patients relating to the clinical disease activity and serum CRP concentration.
Methods Serum CRP and plasma IL‐6 concentrations were measured in 58 CU patients and 30 healthy subjects. Ten CU patients were evaluated twice, during the active period as well as upon the spontaneous clinical remission of the disease. CU activity was assessed with the use of the symptom scores recommended by EAACI/GALEN/EDF guidelines.
Results IL‐6 and CRP concentrations were significantly increased in CU patients as compared with the healthy subjects, whereas they decreased remarkably upon the spontaneous remission. IL‐6 concentration was associated with weekly urticaria activity scores and also significant differences were found between patients showing different degrees of urticarial activity. Significant correlation was observed between IL‐6 and CRP concentrations.
Conclusions and Clinical Relevance This study reinforces evidence that, apart from a local cutaneous inflammation, CU is associated with a systemic inflammatory response. Such acute‐phase response is manifested by increased circulating IL‐6, which varies along with CRP changes and may be related to the urticarial activity.
Cite this as: A. Kasperska‐Zajac, J. Sztylc, E. Machura and G. Jop, Clinical & Experimental Allergy, 2011 (41) 1386–1391. |
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AbstractList | Background
Our previous study was the first to demonstrate enhanced plasma IL‐6 concentrations in chronic urticaria (CU). It is known that C‐reactive protein (CRP) is a sensitive marker of an underlying systemic inflammation, triggered mainly as a response to IL‐6.
Objective
To evaluate plasma IL‐6 concentration in CU patients relating to the clinical disease activity and serum CRP concentration.
Methods
Serum CRP and plasma IL‐6 concentrations were measured in 58 CU patients and 30 healthy subjects. Ten CU patients were evaluated twice, during the active period as well as upon the spontaneous clinical remission of the disease. CU activity was assessed with the use of the symptom scores recommended by EAACI/GALEN/EDF guidelines.
Results
IL‐6 and CRP concentrations were significantly increased in CU patients as compared with the healthy subjects, whereas they decreased remarkably upon the spontaneous remission. IL‐6 concentration was associated with weekly urticaria activity scores and also significant differences were found between patients showing different degrees of urticarial activity. Significant correlation was observed between IL‐6 and CRP concentrations.
Conclusions and Clinical Relevance
This study reinforces evidence that, apart from a local cutaneous inflammation, CU is associated with a systemic inflammatory response. Such acute‐phase response is manifested by increased circulating IL‐6, which varies along with CRP changes and may be related to the urticarial activity.
Cite this as
: A. Kasperska‐Zajac, J. Sztylc, E. Machura and G. Jop,
Clinical & Experimental Allergy
, 2011 (41) 1386–1391. Background Our previous study was the first to demonstrate enhanced plasma IL-6 concentrations in chronic urticaria (CU). It is known that C-reactive protein (CRP) is a sensitive marker of an underlying systemic inflammation, triggered mainly as a response to IL-6. Objective To evaluate plasma IL-6 concentration in CU patients relating to the clinical disease activity and serum CRP concentration. Methods Serum CRP and plasma IL-6 concentrations were measured in 58 CU patients and 30 healthy subjects. Ten CU patients were evaluated twice, during the active period as well as upon the spontaneous clinical remission of the disease. CU activity was assessed with the use of the symptom scores recommended by EAACI/GALEN/EDF guidelines. Results IL-6 and CRP concentrations were significantly increased in CU patients as compared with the healthy subjects, whereas they decreased remarkably upon the spontaneous remission. IL-6 concentration was associated with weekly urticaria activity scores and also significant differences were found between patients showing different degrees of urticarial activity. Significant correlation was observed between IL-6 and CRP concentrations. Conclusions and Clinical Relevance This study reinforces evidence that, apart from a local cutaneous inflammation, CU is associated with a systemic inflammatory response. Such acute-phase response is manifested by increased circulating IL-6, which varies along with CRP changes and may be related to the urticarial activity. Cite this as: A. Kasperska-Zajac, J. Sztylc, E. Machura and G. Jop, Clinical & Experimental Allergy, 2011 (41) 1386-1391. Summary Background Our previous study was the first to demonstrate enhanced plasma IL‐6 concentrations in chronic urticaria (CU). It is known that C‐reactive protein (CRP) is a sensitive marker of an underlying systemic inflammation, triggered mainly as a response to IL‐6. Objective To evaluate plasma IL‐6 concentration in CU patients relating to the clinical disease activity and serum CRP concentration. Methods Serum CRP and plasma IL‐6 concentrations were measured in 58 CU patients and 30 healthy subjects. Ten CU patients were evaluated twice, during the active period as well as upon the spontaneous clinical remission of the disease. CU activity was assessed with the use of the symptom scores recommended by EAACI/GALEN/EDF guidelines. Results IL‐6 and CRP concentrations were significantly increased in CU patients as compared with the healthy subjects, whereas they decreased remarkably upon the spontaneous remission. IL‐6 concentration was associated with weekly urticaria activity scores and also significant differences were found between patients showing different degrees of urticarial activity. Significant correlation was observed between IL‐6 and CRP concentrations. Conclusions and Clinical Relevance This study reinforces evidence that, apart from a local cutaneous inflammation, CU is associated with a systemic inflammatory response. Such acute‐phase response is manifested by increased circulating IL‐6, which varies along with CRP changes and may be related to the urticarial activity. Cite this as: A. Kasperska‐Zajac, J. Sztylc, E. Machura and G. Jop, Clinical & Experimental Allergy, 2011 (41) 1386–1391. Our previous study was the first to demonstrate enhanced plasma IL-6 concentrations in chronic urticaria (CU). It is known that C-reactive protein (CRP) is a sensitive marker of an underlying systemic inflammation, triggered mainly as a response to IL-6. To evaluate plasma IL-6 concentration in CU patients relating to the clinical disease activity and serum CRP concentration. Serum CRP and plasma IL-6 concentrations were measured in 58 CU patients and 30 healthy subjects. Ten CU patients were evaluated twice, during the active period as well as upon the spontaneous clinical remission of the disease. CU activity was assessed with the use of the symptom scores recommended by EAACI/GALEN/EDF guidelines. IL-6 and CRP concentrations were significantly increased in CU patients as compared with the healthy subjects, whereas they decreased remarkably upon the spontaneous remission. IL-6 concentration was associated with weekly urticaria activity scores and also significant differences were found between patients showing different degrees of urticarial activity. Significant correlation was observed between IL-6 and CRP concentrations. This study reinforces evidence that, apart from a local cutaneous inflammation, CU is associated with a systemic inflammatory response. Such acute-phase response is manifested by increased circulating IL-6, which varies along with CRP changes and may be related to the urticarial activity. Summary Background Our previous study was the first to demonstrate enhanced plasma IL-6 concentrations in chronic urticaria (CU). It is known that C-reactive protein (CRP) is a sensitive marker of an underlying systemic inflammation, triggered mainly as a response to IL-6. Objective To evaluate plasma IL-6 concentration in CU patients relating to the clinical disease activity and serum CRP concentration. Methods Serum CRP and plasma IL-6 concentrations were measured in 58 CU patients and 30 healthy subjects. Ten CU patients were evaluated twice, during the active period as well as upon the spontaneous clinical remission of the disease. CU activity was assessed with the use of the symptom scores recommended by EAACI/GALEN/EDF guidelines. Results IL-6 and CRP concentrations were significantly increased in CU patients as compared with the healthy subjects, whereas they decreased remarkably upon the spontaneous remission. IL-6 concentration was associated with weekly urticaria activity scores and also significant differences were found between patients showing different degrees of urticarial activity. Significant correlation was observed between IL-6 and CRP concentrations. Conclusions and Clinical Relevance This study reinforces evidence that, apart from a local cutaneous inflammation, CU is associated with a systemic inflammatory response. Such acute-phase response is manifested by increased circulating IL-6, which varies along with CRP changes and may be related to the urticarial activity. Cite this as: A. Kasperska-Zajac, J. Sztylc, E. Machura and G. Jop, Clinical & Experimental Allergy, 2011 (41) 1386-1391. [PUBLICATION ABSTRACT] Our previous study was the first to demonstrate enhanced plasma IL-6 concentrations in chronic urticaria (CU). It is known that C-reactive protein (CRP) is a sensitive marker of an underlying systemic inflammation, triggered mainly as a response to IL-6.BACKGROUNDOur previous study was the first to demonstrate enhanced plasma IL-6 concentrations in chronic urticaria (CU). It is known that C-reactive protein (CRP) is a sensitive marker of an underlying systemic inflammation, triggered mainly as a response to IL-6.To evaluate plasma IL-6 concentration in CU patients relating to the clinical disease activity and serum CRP concentration.OBJECTIVETo evaluate plasma IL-6 concentration in CU patients relating to the clinical disease activity and serum CRP concentration.Serum CRP and plasma IL-6 concentrations were measured in 58 CU patients and 30 healthy subjects. Ten CU patients were evaluated twice, during the active period as well as upon the spontaneous clinical remission of the disease. CU activity was assessed with the use of the symptom scores recommended by EAACI/GALEN/EDF guidelines.METHODSSerum CRP and plasma IL-6 concentrations were measured in 58 CU patients and 30 healthy subjects. Ten CU patients were evaluated twice, during the active period as well as upon the spontaneous clinical remission of the disease. CU activity was assessed with the use of the symptom scores recommended by EAACI/GALEN/EDF guidelines.IL-6 and CRP concentrations were significantly increased in CU patients as compared with the healthy subjects, whereas they decreased remarkably upon the spontaneous remission. IL-6 concentration was associated with weekly urticaria activity scores and also significant differences were found between patients showing different degrees of urticarial activity. Significant correlation was observed between IL-6 and CRP concentrations.RESULTSIL-6 and CRP concentrations were significantly increased in CU patients as compared with the healthy subjects, whereas they decreased remarkably upon the spontaneous remission. IL-6 concentration was associated with weekly urticaria activity scores and also significant differences were found between patients showing different degrees of urticarial activity. Significant correlation was observed between IL-6 and CRP concentrations.This study reinforces evidence that, apart from a local cutaneous inflammation, CU is associated with a systemic inflammatory response. Such acute-phase response is manifested by increased circulating IL-6, which varies along with CRP changes and may be related to the urticarial activity.CONCLUSIONS AND CLINICAL RELEVANCEThis study reinforces evidence that, apart from a local cutaneous inflammation, CU is associated with a systemic inflammatory response. Such acute-phase response is manifested by increased circulating IL-6, which varies along with CRP changes and may be related to the urticarial activity. |
Author | Sztylc, J. Machura, E. Jop, G. Kasperska-Zajac, A. |
Author_xml | – sequence: 1 givenname: A. surname: Kasperska-Zajac fullname: Kasperska-Zajac, A. organization: Clinical Department of Internal Diseases, Allergology and Clinical Immunology, Medical University of Silesia, Katowice, Poland – sequence: 2 givenname: J. surname: Sztylc fullname: Sztylc, J. organization: Clinical Department of Internal Diseases, Allergology and Clinical Immunology, Medical University of Silesia, Katowice, Poland – sequence: 3 givenname: E. surname: Machura fullname: Machura, E. organization: Department of Pediatric in Zabrze, Medical University of Silesia, Katowice, Poland – sequence: 4 givenname: G. surname: Jop fullname: Jop, G. organization: Clinical Department of Internal Diseases, Allergology and Clinical Immunology, Medical University of Silesia, Katowice, Poland |
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Keywords | Human Skin disease Urticaria Acute Cytokine chronic urticaria C-reactive protein (CRP) acute-phase response Inflammation Concentration Serum protein Biological activity IL-6 Blood plasma Interleukin 6 systemic inflammation Chronic Acute phase protein Immunology Evolution C reactive protein |
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References | Cugno M , TedeschiA, CrostiC, MarzanoAV.Activation of blood coagulation in autoimmune skin disorders. Expert Rev Clin Immunol2009; 5:605-13. Tedeschi A , AseroR, LoriniM, MarzanoAV, CugnoM.Plasma levels of matrix metalloproteinase-9 in chronic urticaria patients correlate with disease severity and C-reactive protein but not with circulating histamine-releasing factors. Clin Exp Allergy2010; 40:875-81. Fujii K , KonishiK, KannoY, OhgouN.Acute urticaria with elevated circulating interleukin-6 is resistant to anti-histamine treatment. J Dermatol2001; 28:248-50. Kaplan A. Inflammation in chronic urticaria is not limited to the consequences of mast cell (or basophil) degranulation. Clin Exp Allergy2010; 40:834-5. Kasperska-Zajac A , BrzozaZ, RogalaB.Plasma concentration of interleukin 6 (IL-6), and its relationship with circulating concentration of dehydroepiandrosterone sulfate (DHEA-S) in patients with chronic idiopathic urticaria. Cytokine2007; 39:142-6. Altrichter S , BoodsteinN, MaurerM.Matrix metalloproteinase-9: a novel biomarker for monitoring disease activity in patients with chronic urticaria patients? Allergy 2009; 64:652-6. Zuberbier T , AseroR, Bindslev-JensenCet al. Dermatology Section of the European Academy of Allergology and Clinical Immunology; Global Allergy and Asthma European Network; European Dermatology Forum; World Allergy Organization. EAACI/GA(2)LEN/EDF/WAO guideline: definition, classification and diagnosis of urticaria. Allergy 2009; 64:1417-26. Lawlor F , BirdC, CampRDet al. Increased interleukin 6, but reduced interleukin 1, in delayed pressure urticaria. Br J Dermatol1993; 128:500-3. Danesh J , WheelerJG, HirschfieldGMet al. C-reactive protein and other circulating markers of inflammation in the prediction of coronary heart disease. N Engl J Med2004; 350:1387-97. Konstantinou GN , AseroR, MaurerM, SabroeRA, Schmid-GrendelmeierP, GrattanCE.EAACI/GA(2)LEN task force consensus report: the autologous serum skin test in urticaria. Allergy 2009; 64:1256-68. Sabroe RA , GrattanCEH, FrancisDM, BarrRM, Kobza BlackA, GreavesMW.The autologous serum skin test: a screening test for autoantibodies in chronic idiopathic urticatia. Br J Dermatol 1999; 140:446-53. Takahagi S , MiharaS, IwamotoKet al. Coagulation/fibrinolysis and inflammation markers are associated with disease activity in patients with chronic urticaria. Allergy2010; 65:649-56. Seder RA , PaulWE, Ben-SassonSZet al. Production of interleukin-4 and other cytokines following stimulation of mast cell lines and in vivo mast cells/basophils. Int Arch Allergy Appl Immunol1991; 94:137-40. Haverkate F , ThompsonSG, PykeSDet al. Production of C-reactive protein and risk of coronary events in stable and unstable angina. European Concerted Action on Thrombosis and Disabilities Angina Pectoris Study Group. Lancet1997; 349:462-6. Nettis E , DambraP, LoriaMPet al. Mast-cell phenotype in urticaria. Allergy2001; 56:915. Volanakis JE. Human C-reactive protein: expression, structure, and function. Mol Immunol 2001; 38:189-97. Asero R , TedeschiA, CoppolaRet al. Activation of the tissue pathway of blood coagulation in patients with chronic urticaria. J Allergy Clin Immunol2007; 119:705-10. Gabay C. Interleukin-6 and chronic inflammation. Arthritis Res Ther2006; 8(Suppl. 2):S3. Sehgal PB. Interleukin-6: molecular pathophysiology. J Invest Dermatol 1990; 94:2S-6S. Gabay C , KushnerI.Acute-phase proteins and other systemic responses to inflammation. N Engl J Med1999; 340:448-54. Fujii K , OhgouN.Up-regulation of IL-6 mRNA in peripheral blood mononuclear cells of patients with acute urticaria. J Dermatol2004; 31:242-3. Asero R , TedeschiA, RiboldiP, GriffiniS, BonanniE, CugnoM.Severe chronic urticaria is associated with elevated plasma levels of D-dimer. Allergy2008; 63:176-80. 2007; 39 2010; 65 2004; 31 1993; 128 2007; 119 1997; 349 2009; 64 2004; 350 1991; 94 1999; 340 2006; 8 1999; 140 2001; 38 2001; 28 2009; 5 2008; 63 2001; 56 2010; 40 1990; 94 e_1_2_6_20_2 Zuberbier T (e_1_2_6_10_2) 2009; 64 Gabay C. (e_1_2_6_5_2) 2006; 8 Konstantinou GN (e_1_2_6_16_2) 2009; 64 Altrichter S (e_1_2_6_11_2) 2009; 64 e_1_2_6_7_2 e_1_2_6_18_2 Volanakis JE. (e_1_2_6_6_2) 2001; 38 e_1_2_6_9_2 e_1_2_6_19_2 e_1_2_6_4_2 e_1_2_6_3_2 e_1_2_6_13_2 e_1_2_6_23_2 e_1_2_6_2_2 e_1_2_6_22_2 Sehgal PB. (e_1_2_6_8_2) 1990; 94 e_1_2_6_21_2 Sabroe RA (e_1_2_6_12_2) 1999; 140 e_1_2_6_17_2 e_1_2_6_14_2 e_1_2_6_15_2 |
References_xml | – reference: Danesh J , WheelerJG, HirschfieldGMet al. C-reactive protein and other circulating markers of inflammation in the prediction of coronary heart disease. N Engl J Med2004; 350:1387-97. – reference: Kaplan A. Inflammation in chronic urticaria is not limited to the consequences of mast cell (or basophil) degranulation. Clin Exp Allergy2010; 40:834-5. – reference: Seder RA , PaulWE, Ben-SassonSZet al. Production of interleukin-4 and other cytokines following stimulation of mast cell lines and in vivo mast cells/basophils. Int Arch Allergy Appl Immunol1991; 94:137-40. – reference: Konstantinou GN , AseroR, MaurerM, SabroeRA, Schmid-GrendelmeierP, GrattanCE.EAACI/GA(2)LEN task force consensus report: the autologous serum skin test in urticaria. Allergy 2009; 64:1256-68. – reference: Lawlor F , BirdC, CampRDet al. Increased interleukin 6, but reduced interleukin 1, in delayed pressure urticaria. Br J Dermatol1993; 128:500-3. – reference: Sabroe RA , GrattanCEH, FrancisDM, BarrRM, Kobza BlackA, GreavesMW.The autologous serum skin test: a screening test for autoantibodies in chronic idiopathic urticatia. Br J Dermatol 1999; 140:446-53. – reference: Asero R , TedeschiA, CoppolaRet al. Activation of the tissue pathway of blood coagulation in patients with chronic urticaria. J Allergy Clin Immunol2007; 119:705-10. – reference: Fujii K , OhgouN.Up-regulation of IL-6 mRNA in peripheral blood mononuclear cells of patients with acute urticaria. J Dermatol2004; 31:242-3. – reference: Haverkate F , ThompsonSG, PykeSDet al. Production of C-reactive protein and risk of coronary events in stable and unstable angina. European Concerted Action on Thrombosis and Disabilities Angina Pectoris Study Group. Lancet1997; 349:462-6. – reference: Volanakis JE. Human C-reactive protein: expression, structure, and function. Mol Immunol 2001; 38:189-97. – reference: Gabay C , KushnerI.Acute-phase proteins and other systemic responses to inflammation. N Engl J Med1999; 340:448-54. – reference: Fujii K , KonishiK, KannoY, OhgouN.Acute urticaria with elevated circulating interleukin-6 is resistant to anti-histamine treatment. J Dermatol2001; 28:248-50. – reference: Cugno M , TedeschiA, CrostiC, MarzanoAV.Activation of blood coagulation in autoimmune skin disorders. Expert Rev Clin Immunol2009; 5:605-13. – reference: Gabay C. Interleukin-6 and chronic inflammation. Arthritis Res Ther2006; 8(Suppl. 2):S3. – reference: Takahagi S , MiharaS, IwamotoKet al. Coagulation/fibrinolysis and inflammation markers are associated with disease activity in patients with chronic urticaria. Allergy2010; 65:649-56. – reference: Zuberbier T , AseroR, Bindslev-JensenCet al. Dermatology Section of the European Academy of Allergology and Clinical Immunology; Global Allergy and Asthma European Network; European Dermatology Forum; World Allergy Organization. EAACI/GA(2)LEN/EDF/WAO guideline: definition, classification and diagnosis of urticaria. Allergy 2009; 64:1417-26. – reference: Tedeschi A , AseroR, LoriniM, MarzanoAV, CugnoM.Plasma levels of matrix metalloproteinase-9 in chronic urticaria patients correlate with disease severity and C-reactive protein but not with circulating histamine-releasing factors. Clin Exp Allergy2010; 40:875-81. – reference: Sehgal PB. Interleukin-6: molecular pathophysiology. J Invest Dermatol 1990; 94:2S-6S. – reference: Asero R , TedeschiA, RiboldiP, GriffiniS, BonanniE, CugnoM.Severe chronic urticaria is associated with elevated plasma levels of D-dimer. Allergy2008; 63:176-80. – reference: Kasperska-Zajac A , BrzozaZ, RogalaB.Plasma concentration of interleukin 6 (IL-6), and its relationship with circulating concentration of dehydroepiandrosterone sulfate (DHEA-S) in patients with chronic idiopathic urticaria. Cytokine2007; 39:142-6. – reference: Altrichter S , BoodsteinN, MaurerM.Matrix metalloproteinase-9: a novel biomarker for monitoring disease activity in patients with chronic urticaria patients? Allergy 2009; 64:652-6. – reference: Nettis E , DambraP, LoriaMPet al. Mast-cell phenotype in urticaria. Allergy2001; 56:915. – volume: 94 start-page: 137 year: 1991 end-page: 40 article-title: Production of interleukin‐4 and other cytokines following stimulation of mast cell lines and in vivo mast cells/basophils publication-title: Int Arch Allergy Appl Immunol – volume: 40 start-page: 875 year: 2010 end-page: 81 article-title: Plasma levels of matrix metalloproteinase‐9 in chronic urticaria patients correlate with disease severity and C‐reactive protein but not with circulating histamine‐releasing factors publication-title: Clin Exp Allergy – volume: 65 start-page: 649 year: 2010 end-page: 56 article-title: Coagulation/fibrinolysis and inflammation markers are associated with disease activity in patients with chronic urticaria publication-title: Allergy – volume: 94 start-page: 2S year: 1990 end-page: 6S article-title: Interleukin‐6 publication-title: molecular pathophysiology – volume: 63 start-page: 176 year: 2008 end-page: 80 article-title: Severe chronic urticaria is associated with elevated plasma levels of D‐dimer publication-title: Allergy – volume: 56 start-page: 915 year: 2001 article-title: Mast‐cell phenotype in urticaria publication-title: Allergy – volume: 8 start-page: S3 issue: (Suppl. 2) year: 2006 article-title: Interleukin‐6 and chronic inflammation publication-title: Arthritis Res Ther – volume: 28 start-page: 248 year: 2001 end-page: 50 article-title: Acute urticaria with elevated circulating interleukin‐6 is resistant to anti‐histamine treatment publication-title: J Dermatol – volume: 39 start-page: 142 year: 2007 end-page: 6 article-title: Plasma concentration of interleukin 6 (IL‐6), and its relationship with circulating concentration of dehydroepiandrosterone sulfate (DHEA‐S) in patients with chronic idiopathic urticaria publication-title: Cytokine – volume: 5 start-page: 605 year: 2009 end-page: 13 article-title: Activation of blood coagulation in autoimmune skin disorders publication-title: Expert Rev Clin Immunol – volume: 119 start-page: 705 year: 2007 end-page: 10 article-title: Activation of the tissue pathway of blood coagulation in patients with chronic urticaria publication-title: J Allergy Clin Immunol – volume: 140 start-page: 446 year: 1999 end-page: 53 article-title: The autologous serum skin test publication-title: a screening test for autoantibodies in chronic idiopathic urticatia – volume: 349 start-page: 462 year: 1997 end-page: 6 article-title: Production of C‐reactive protein and risk of coronary events in stable and unstable angina. European Concerted Action on Thrombosis and Disabilities Angina Pectoris Study Group publication-title: Lancet – volume: 31 start-page: 242 year: 2004 end-page: 3 article-title: Up‐regulation of IL‐6 mRNA in peripheral blood mononuclear cells of patients with acute urticaria publication-title: J Dermatol – volume: 64 start-page: 1256 year: 2009 end-page: 68 article-title: EAACI/GA(2)LEN task force consensus report publication-title: the autologous serum skin test in urticaria – volume: 350 start-page: 1387 year: 2004 end-page: 97 article-title: C‐reactive protein and other circulating markers of inflammation in the prediction of coronary heart disease publication-title: N Engl J Med – volume: 40 start-page: 834 year: 2010 end-page: 5 article-title: Inflammation in chronic urticaria is not limited to the consequences of mast cell (or basophil) degranulation publication-title: Clin Exp Allergy – volume: 38 start-page: 189 year: 2001 end-page: 97 article-title: Human C‐reactive protein publication-title: expression, structure, and function – volume: 128 start-page: 500 year: 1993 end-page: 3 article-title: Increased interleukin 6, but reduced interleukin 1, in delayed pressure urticaria publication-title: Br J Dermatol – volume: 340 start-page: 448 year: 1999 end-page: 54 article-title: Acute‐phase proteins and other systemic responses to inflammation publication-title: N Engl J Med – volume: 64 start-page: 1417 year: 2009 end-page: 26 article-title: Dermatology Section of the European Academy of Allergology and Clinical Immunology; Global Allergy and Asthma European Network; European Dermatology Forum; World Allergy Organization. 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EAACI/GA(2)LEN/EDF/WAO guideline publication-title: definition, classification and diagnosis of urticaria – volume: 64 start-page: 652 year: 2009 ident: e_1_2_6_11_2 article-title: Matrix metalloproteinase‐9 publication-title: a novel biomarker for monitoring disease activity in patients with chronic urticaria patients? – volume: 8 start-page: S3 issue: 2 year: 2006 ident: e_1_2_6_5_2 article-title: Interleukin‐6 and chronic inflammation publication-title: Arthritis Res Ther doi: 10.1186/ar1917 |
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Background Our previous study was the first to demonstrate enhanced plasma IL‐6 concentrations in chronic urticaria (CU). It is known that C‐reactive... Background Our previous study was the first to demonstrate enhanced plasma IL‐6 concentrations in chronic urticaria (CU). It is known that C‐reactive protein... Our previous study was the first to demonstrate enhanced plasma IL-6 concentrations in chronic urticaria (CU). It is known that C-reactive protein (CRP) is a... Summary Background Our previous study was the first to demonstrate enhanced plasma IL-6 concentrations in chronic urticaria (CU). It is known that C-reactive... Background Our previous study was the first to demonstrate enhanced plasma IL-6 concentrations in chronic urticaria (CU). It is known that C-reactive protein... |
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SubjectTerms | Acute-Phase Reaction acute-phase response Adult Allergic diseases Biological and medical sciences Biomarkers - blood C-reactive protein (CRP) C-Reactive Protein - metabolism Chronic Disease chronic urticaria Female Fundamental and applied biological sciences. Psychology Fundamental immunology Humans IL-6 Immunopathology Inflammation - blood Interleukin-6 - blood Male Medical research Medical sciences Plasma Severity of Illness Index Skin allergic diseases. Stinging insect allergies systemic inflammation Urticaria - blood Urticaria - physiopathology |
Title | Plasma IL-6 concentration correlates with clinical disease activity and serum C-reactive protein concentration in chronic urticaria patients |
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