Complement activation in patients with primary antiphospholipid syndrome
Objective:To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS).Methods:Thirty-six patients with primary APS, 42 control patients with non-systemic lupus erythematosus (SLE) connective tissue diseases, and 36 healthy volunteers were analyse...
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Published in | Annals of the rheumatic diseases Vol. 68; no. 6; pp. 1030 - 1035 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
BMJ Publishing Group Ltd and European League Against Rheumatism
01.06.2009
BMJ Publishing Group Elsevier Limited |
Subjects | |
Online Access | Get full text |
ISSN | 0003-4967 1468-2060 1468-2060 |
DOI | 10.1136/ard.2008.090670 |
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Abstract | Objective:To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS).Methods:Thirty-six patients with primary APS, 42 control patients with non-systemic lupus erythematosus (SLE) connective tissue diseases, and 36 healthy volunteers were analysed retrospectively. Serum complement levels (C3, C4, CH50) and anaphylatoxins (C3a, C4a, C5a) were examined in all subjects, and serum complement regulatory factors (factor H and factor I) were measured in patients with primary APS. Plasma anticoagulant activity was determined in a mixing test using the activated partial thromboplastin time.Results:Serum complement levels were significantly lower in patients with primary APS than in patients with non-SLE connective tissue diseases (mean (SD) C3: 81.07 (17.86) vs 109.80 (22.76) mg/dl, p<0.001; C4: 13.04 (8.49) vs 21.70 (6.96) mg/dl, p<0.001; CH50: 31.32 (8.76) vs 41.40 (7.70) U/ml, p<0.001) or healthy volunteers. Only two healthy subjects with low serum C4 levels showed hypocomplementaemia, whereas most patients with primary APS showed raised serum C3a and C4a. No subjects showed raised C5a. Patients with primary APS with low serum C3 or C4 had significantly higher levels of C3a or C4a than healthy controls. No patients had low serum complement regulatory factors. Among patients with primary APS, hypocomplementaemia was significantly more common in those with high anticoagulant activity than in those with low or normal activity.Conclusion:Hypocomplementaemia is common in patients with primary APS, reflecting complement activation and consumption, and was correlated with anticoagulant activity, suggesting that antiphospholipid antibodies may activate monocytes and macrophages via anaphylatoxins produced in complement activation. |
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AbstractList | To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS).
Thirty-six patients with primary APS, 42 control patients with non-systemic lupus erythematosus (SLE) connective tissue diseases, and 36 healthy volunteers were analysed retrospectively. Serum complement levels (C3, C4, CH(50)) and anaphylatoxins (C3a, C4a, C5a) were examined in all subjects, and serum complement regulatory factors (factor H and factor I) were measured in patients with primary APS. Plasma anticoagulant activity was determined in a mixing test using the activated partial thromboplastin time.
Serum complement levels were significantly lower in patients with primary APS than in patients with non-SLE connective tissue diseases (mean (SD) C3: 81.07 (17.86) vs 109.80 (22.76) mg/dl, p<0.001; C4: 13.04 (8.49) vs 21.70 (6.96) mg/dl, p<0.001; CH(50): 31.32 (8.76) vs 41.40 (7.70) U/ml, p<0.001) or healthy volunteers. Only two healthy subjects with low serum C4 levels showed hypocomplementaemia, whereas most patients with primary APS showed raised serum C3a and C4a. No subjects showed raised C5a. Patients with primary APS with low serum C3 or C4 had significantly higher levels of C3a or C4a than healthy controls. No patients had low serum complement regulatory factors. Among patients with primary APS, hypocomplementaemia was significantly more common in those with high anticoagulant activity than in those with low or normal activity.
Hypocomplementaemia is common in patients with primary APS, reflecting complement activation and consumption, and was correlated with anticoagulant activity, suggesting that antiphospholipid antibodies may activate monocytes and macrophages via anaphylatoxins produced in complement activation. Objective: To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS). Methods: Thirty-six patients with primary APS, 42 control patients with non-systemic lupus erythematosus (SLE) connective tissue diseases, and 36 healthy volunteers were analysed retrospectively. Serum complement levels (C3, C4, CH50) and anaphylatoxins (C3a, C4a, C5a) were examined in all subjects, and serum complement regulatory factors (factor H and factor I) were measured in patients with primary APS. Plasma anticoagulant activity was determined in a mixing test using the activated partial thromboplastin time. Results: Serum complement levels were significantly lower in patients with primary APS than in patients with non-SLE connective tissue diseases (mean (SD) C3: 81.07 (17.86) vs 109.80 (22.76) mg/dl, p<0.001; C4: 13.04 (8.49) vs 21.70 (6.96) mg/dl, p<0.001; CH50: 31.32 (8.76) vs 41.40 (7.70) U/ml, p<0.001) or healthy volunteers. Only two healthy subjects with low serum C4 levels showed hypocomplementaemia, whereas most patients with primary APS showed raised serum C3a and C4a. No subjects showed raised C5a. Patients with primary APS with low serum C3 or C4 had significantly higher levels of C3a or C4a than healthy controls. No patients had low serum complement regulatory factors. Among patients with primary APS, hypocomplementaemia was significantly more common in those with high anticoagulant activity than in those with low or normal activity. Conclusion: Hypocomplementaemia is common in patients with primary APS, reflecting complement activation and consumption, and was correlated with anticoagulant activity, suggesting that antiphospholipid antibodies may activate monocytes and macrophages via anaphylatoxins produced in complement activation. To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS).OBJECTIVETo investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS).Thirty-six patients with primary APS, 42 control patients with non-systemic lupus erythematosus (SLE) connective tissue diseases, and 36 healthy volunteers were analysed retrospectively. Serum complement levels (C3, C4, CH(50)) and anaphylatoxins (C3a, C4a, C5a) were examined in all subjects, and serum complement regulatory factors (factor H and factor I) were measured in patients with primary APS. Plasma anticoagulant activity was determined in a mixing test using the activated partial thromboplastin time.METHODSThirty-six patients with primary APS, 42 control patients with non-systemic lupus erythematosus (SLE) connective tissue diseases, and 36 healthy volunteers were analysed retrospectively. Serum complement levels (C3, C4, CH(50)) and anaphylatoxins (C3a, C4a, C5a) were examined in all subjects, and serum complement regulatory factors (factor H and factor I) were measured in patients with primary APS. Plasma anticoagulant activity was determined in a mixing test using the activated partial thromboplastin time.Serum complement levels were significantly lower in patients with primary APS than in patients with non-SLE connective tissue diseases (mean (SD) C3: 81.07 (17.86) vs 109.80 (22.76) mg/dl, p<0.001; C4: 13.04 (8.49) vs 21.70 (6.96) mg/dl, p<0.001; CH(50): 31.32 (8.76) vs 41.40 (7.70) U/ml, p<0.001) or healthy volunteers. Only two healthy subjects with low serum C4 levels showed hypocomplementaemia, whereas most patients with primary APS showed raised serum C3a and C4a. No subjects showed raised C5a. Patients with primary APS with low serum C3 or C4 had significantly higher levels of C3a or C4a than healthy controls. No patients had low serum complement regulatory factors. Among patients with primary APS, hypocomplementaemia was significantly more common in those with high anticoagulant activity than in those with low or normal activity.RESULTSSerum complement levels were significantly lower in patients with primary APS than in patients with non-SLE connective tissue diseases (mean (SD) C3: 81.07 (17.86) vs 109.80 (22.76) mg/dl, p<0.001; C4: 13.04 (8.49) vs 21.70 (6.96) mg/dl, p<0.001; CH(50): 31.32 (8.76) vs 41.40 (7.70) U/ml, p<0.001) or healthy volunteers. Only two healthy subjects with low serum C4 levels showed hypocomplementaemia, whereas most patients with primary APS showed raised serum C3a and C4a. No subjects showed raised C5a. Patients with primary APS with low serum C3 or C4 had significantly higher levels of C3a or C4a than healthy controls. No patients had low serum complement regulatory factors. Among patients with primary APS, hypocomplementaemia was significantly more common in those with high anticoagulant activity than in those with low or normal activity.Hypocomplementaemia is common in patients with primary APS, reflecting complement activation and consumption, and was correlated with anticoagulant activity, suggesting that antiphospholipid antibodies may activate monocytes and macrophages via anaphylatoxins produced in complement activation.CONCLUSIONHypocomplementaemia is common in patients with primary APS, reflecting complement activation and consumption, and was correlated with anticoagulant activity, suggesting that antiphospholipid antibodies may activate monocytes and macrophages via anaphylatoxins produced in complement activation. |
Author | Horita, T Atsumi, T Kataoka, H Amengual, O Oku, K Yasuda, S Bohgaki, M Koike, T |
Author_xml | – sequence: 1 givenname: K surname: Oku fullname: Oku, K email: at3tat@med.hokudai.ac.jp – sequence: 2 givenname: T surname: Atsumi fullname: Atsumi, T email: at3tat@med.hokudai.ac.jp – sequence: 3 givenname: M surname: Bohgaki fullname: Bohgaki, M email: at3tat@med.hokudai.ac.jp – sequence: 4 givenname: O surname: Amengual fullname: Amengual, O email: at3tat@med.hokudai.ac.jp – sequence: 5 givenname: H surname: Kataoka fullname: Kataoka, H email: at3tat@med.hokudai.ac.jp – sequence: 6 givenname: T surname: Horita fullname: Horita, T email: at3tat@med.hokudai.ac.jp – sequence: 7 givenname: S surname: Yasuda fullname: Yasuda, S email: at3tat@med.hokudai.ac.jp – sequence: 8 givenname: T surname: Koike fullname: Koike, T email: at3tat@med.hokudai.ac.jp |
BackLink | http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21479746$$DView record in Pascal Francis https://www.ncbi.nlm.nih.gov/pubmed/18625630$$D View this record in MEDLINE/PubMed |
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Cites_doi | 10.4049/jimmunol.160.11.5572 10.1056/NEJM200104053441406 10.1038/nm1121 10.4049/jimmunol.174.5.3041 10.1002/1529-0131(199907)42:7<1309::AID-ANR1>3.0.CO;2-F 10.1016/j.clim.2007.05.010 10.1093/intimm/dxh166 10.1002/1529-0131(199808)41:8<1513::AID-ART28>3.0.CO;2-7 10.4049/jimmunol.174.1.485 10.1111/j.1538-7836.2006.01753.x 10.1016/j.cca.2006.06.010 10.1161/01.CIR.99.15.1997 10.4049/jimmunol.177.7.4794 10.1093/rheumatology/35.12.1239 10.1182/blood-2002-08-2349 10.1182/blood-2004-01-0145 10.1002/art.1780290905 10.1055/s-0037-1615676 10.1080/14767050500072722 10.1078/0171-2985-00214 10.1002/1529-0131(200009)43:9<1982::AID-ANR9>3.0.CO;2-2 10.1093/rheumatology/40.9.1026 10.1002/art.1780400928 10.1002/art.20434 10.1055/s-0038-1649901 10.1002/1529-0131(199901)42:1<167::AID-ANR20>3.0.CO;2-B 10.1093/clinchem/45.8.1190 10.1084/jem.158.2.603 10.1111/j.1538-7836.2006.02065.x 10.1046/j.1538-7836.2003.00303.x 10.1016/0161-5890(80)90067-X 10.1002/anr.1780320305 10.1172/JCI200318817 10.1111/j.1365-2249.1992.tb05864.x 10.1016/B9-78-012433-9/01950-0429 10.1038/ncprheum0432 10.1046/j.1365-2249.1998.00582.x 10.1038/ki.1983.225 10.1056/NEJM198102263040901 10.1046/j.1365-2141.2002.03928.x |
ContentType | Journal Article |
Copyright | 2009 BMJ Publishing Group and European League Against Rheumatism 2009 INIST-CNRS Copyright: 2009 2009 BMJ Publishing Group and European League Against Rheumatism |
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ISSN | 0003-4967 1468-2060 |
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Keywords | Vascular disease Human Immunopathology Platelet Antiphospholipid antibody syndrome Rheumatology Autoimmune disease Cardiovascular disease Hemopathy Activation |
Language | English |
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PublicationTitle | Annals of the rheumatic diseases |
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References | Pierangeli, Colden-Stanfield, Liu, Barker, Anderson, Harris 1999; 99 Weeks, Moratz, Zacharia, Stracener, Egan, Peckham 2007; 124 Zhou, Wolberg, Roubey 2004; 104 Vega-Ostertag, Harris, Pierangeli 2004; 50 Ieko, Ichikawa, Triplett, Matsuura, Atsumi, Sawada 1999; 42 Forastiero, Martinuzzo, Lu, Broze 2003; 1 Richani, Soto, Romero, Espinoza, Chaiworapongsa, Nien 2005; 17 Bohgaki, Atsumi, Yamashita, Yasuda, Sakai, Furusaki 2004; 16 Atsumi, Ieko, Bertolaccini, Ichikawa, Tsutsumi, Matsuura 2000; 43 Atsumi, Khamashta, Amengual, Donohoe, Mackie, Ichikawa 1998; 112 Amengual, Atsumi, Khamashta, Koike, Hughes 1996; 35 Hammond, Rudge, Loizou, Bowcock, Walport 1989; 32 Girardi, Berman, Redecha, Spruce, Thurman, Kraus 2003; 112 Belmont, Hopkins, Edelson, Kaplan, Ludewig, Weissmann 1986; 29 Wilson, Gharavi, Koike, Lockshin, Branch, Piette 1999; 42 Hochberg 1997; 40 Walport 2001; 344 Matuura, Kobayashi, Koike, Shoenfeld, Khamashta, Hughes 2003; 207 Takeuchi, Atsumi, Ieko, Amasaki, Ichikawa, Koike 2002; 119 Loizou, Cofiner, Weetman, Walport 1992; 90 Samarkos, Davies, Gordon, Walport, Loizou 2001; 40 Ritis, Doumas, Mastellos, Micheli, Giaglis, Magotti 2006; 177 Del Papa, Sheng, Raschi, Kandiah, Tincani, Khamashta 1998; 160 Polley, Nachman 1983; 158 Chenoweth, Cooper, Hugli, Stewart, Blackstone, Kirklin 1981; 304 Peerschke, Yin, Grigg, Ghebrehiwet 2006; 4 Skokowa, Ali, Felda, Kumar, Konrad, Shushakova 2005; 174 Chenoweth, Hugli 1980; 17 Salmon, Girardi, Lockshin 2007; 3 Arumugam, Magnus, Woodruff, Proctor, Shiels, Taylor 2006; 374 Raschi, Testoni, Bosisio, Borghi, Koike, Mantovani 2003; 101 Amengual, Atsumi, Khamashta, Bertolaccini, Hughes 1998; 41 Brandt, Triplett, Alving, Scharrer 1995; 74 Berman, Girardi, Salmon 2005; 174 Girardi, Redecha, Salmon 2004; 10 Miyakis, Lockshin, Atsumi, Branch, Brey, Cervera 2006; 4 Harris, Gharavi, Patel, Hughes 1987; 68 Pfeifer, Kawahara, Hugli 1999; 45 Chenoweth, Cheung, Henderson 1983; 24 Bertolaccini, Atsumi, Lanchbury, Caliz, Katsumata, Vaughan 2001; 85 Hochberg (10.1136/ard.2008.090670_bib22) 1997; 40 Peerschke (10.1136/ard.2008.090670_bib35) 2006; 4 Del Papa (10.1136/ard.2008.090670_bib5) 1998; 160 Hammond (10.1136/ard.2008.090670_bib39) 1989; 32 Arumugam (10.1136/ard.2008.090670_bib33) 2006; 374 Chenoweth (10.1136/ard.2008.090670_bib16) 1980; 17 Chenoweth (10.1136/ard.2008.090670_bib28) 1981; 304 Ieko (10.1136/ard.2008.090670_bib12) 1999; 42 Berman (10.1136/ard.2008.090670_bib41) 2005; 174 Raschi (10.1136/ard.2008.090670_bib3) 2003; 101 Skokowa (10.1136/ard.2008.090670_bib17) 2005; 174 Belmont (10.1136/ard.2008.090670_bib30) 1986; 29 Miyakis (10.1136/ard.2008.090670_bib1) 2006; 4 Pierangeli (10.1136/ard.2008.090670_bib6) 1999; 99 Salmon (10.1136/ard.2008.090670_bib20) 2007; 3 Wilson (10.1136/ard.2008.090670_bib21) 1999; 42 Weeks (10.1136/ard.2008.090670_bib34) 2007; 124 Ritis (10.1136/ard.2008.090670_bib32) 2006; 177 Bertolaccini (10.1136/ard.2008.090670_bib40) 2001; 85 Forastiero (10.1136/ard.2008.090670_bib13) 2003; 1 Girardi (10.1136/ard.2008.090670_bib18) 2003; 112 Brandt (10.1136/ard.2008.090670_bib27) 1995; 74 Polley (10.1136/ard.2008.090670_bib15) 1983; 158 Zhou (10.1136/ard.2008.090670_bib8) 2004; 104 Walport (10.1136/ard.2008.090670_bib14) 2001; 344 Atsumi (10.1136/ard.2008.090670_bib11) 1998; 112 Bohgaki (10.1136/ard.2008.090670_bib4) 2004; 16 Takeuchi (10.1136/ard.2008.090670_bib10) 2002; 119 Vega-Ostertag (10.1136/ard.2008.090670_bib9) 2004; 50 Pfeifer (10.1136/ard.2008.090670_bib23) 1999; 45 Atsumi (10.1136/ard.2008.090670_bib2) 2004 Richani (10.1136/ard.2008.090670_bib31) 2005; 17 Matuura (10.1136/ard.2008.090670_bib36) 2003; 207 Harris (10.1136/ard.2008.090670_bib24) 1987; 68 Atsumi (10.1136/ard.2008.090670_bib26) 2000; 43 Chenoweth (10.1136/ard.2008.090670_bib29) 1983; 24 Girardi (10.1136/ard.2008.090670_bib19) 2004; 10 Amengual (10.1136/ard.2008.090670_bib25) 1996; 35 Samarkos (10.1136/ard.2008.090670_bib38) 2001; 40 Amengual (10.1136/ard.2008.090670_bib7) 1998; 41 Loizou (10.1136/ard.2008.090670_bib37) 1992; 90 |
References_xml | – volume: 50 start-page: 2911 year: 2004 article-title: Intracellular events in platelet activation induced by antiphospholipid antibodies in the presence of low doses of thrombin. publication-title: Arthritis Rheum – volume: 41 start-page: 1513 year: 1998 article-title: IgG2 restriction of anti-beta2-glycoprotein I as the basis for the association between IgG2 anticardiolipin antibodies and thrombosis in the antiphospholipid syndrome. publication-title: Arthritis Rheum – volume: 304 start-page: 497 year: 1981 article-title: Complement activation during cardiopulmonary bypass: evidence for generation of C3a and C5a anaphylatoxins. publication-title: N Engl J Med – volume: 177 start-page: 4794 year: 2006 article-title: A novel C5a receptor-tissue factor cross-talk in neutrophils links innate immunity to coagulation pathways. publication-title: J Immunol – volume: 99 start-page: 1997 year: 1999 article-title: Antiphospholipid antibodies from antiphospholipid syndrome patients activate endothelial cells in vitro and in vivo. publication-title: Circulation – volume: 42 start-page: 167 year: 1999 article-title: Beta2-glycoprotein I is necessary to inhibit protein C activity by monoclonal anticardiolipin antibodies. publication-title: Arthritis Rheum – volume: 90 start-page: 434 year: 1992 article-title: Immunoglobulin class and IgG subclass distribution of antiphospholipid antibodies in patients with systemic lupus erythematosus and associated disorders. publication-title: Clin Exp Immunol – volume: 68 start-page: 215 year: 1987 article-title: Evaluation of the anti-cardiolipin antibody test: report of an international workshop held 4 April 1986. publication-title: Clin Exp Immunol – volume: 3 start-page: 140 year: 2007 article-title: The antiphospholipid syndrome as a disorder initiated by inflammation: implications for the therapy of pregnant patients. publication-title: Nat Clin Pract Rheumatol – volume: 85 start-page: 198 year: 2001 article-title: Plasma tumor necrosis factor alpha levels and the −238*A promoter polymorphism in patients with antiphospholipid syndrome. publication-title: Thromb Haemost – volume: 40 start-page: 1026 year: 2001 article-title: IgG subclass distribution of antibodies against beta(2)-GP1 and cardiolipin in patients with systemic lupus erythematosus and primary antiphospholipid syndrome, and their clinical associations. publication-title: Rheumatology (Oxford) – volume: 112 start-page: 1644 year: 2003 article-title: Complement C5a receptors and neutrophils mediate fetal injury in the antiphospholipid syndrome. publication-title: J Clin Invest – volume: 74 start-page: 1185 year: 1995 article-title: Criteria for the diagnosis of lupus anticoagulants: an update. On behalf of the Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibody of the Scientific and Standardisation Committee of the ISTH. publication-title: Thromb Haemost – volume: 174 start-page: 485 year: 2005 article-title: TNF-alpha is a critical effector and a target for therapy in antiphospholipid antibody-induced pregnancy loss. publication-title: J Immunol – volume: 42 start-page: 1309 year: 1999 article-title: International consensus statement on preliminary classification criteria for definite antiphospholipid syndrome: report of an international workshop. publication-title: Arthritis Rheum – volume: 112 start-page: 325 year: 1998 article-title: Binding of anticardiolipin antibodies to protein C via beta2-glycoprotein I (beta2-GPI): a possible mechanism in the inhibitory effect of antiphospholipid antibodies on the protein C system. publication-title: Clin Exp Immunol – volume: 35 start-page: 1239 year: 1996 article-title: Specificity of ELISA for antibody to beta 2-glycoprotein I in patients with antiphospholipid syndrome. publication-title: Br J Rheumatol – volume: 4 start-page: 2035 year: 2006 article-title: Blood platelets activate the classical pathway of human complement. publication-title: J Thromb Haemost – volume: 4 start-page: 295 year: 2006 article-title: International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS). publication-title: J Thromb Haemost – volume: 158 start-page: 603 year: 1983 article-title: Human platelet activation by C3a and C3a des-Arg. publication-title: J Exp Med – volume: 10 start-page: 1222 year: 2004 article-title: Heparin prevents antiphospholipid antibody-induced fetal loss by inhibiting complement activation. publication-title: Nat Med – volume: 45 start-page: 1190 year: 1999 article-title: Possible mechanism for in vitro complement activation in blood and plasma samples: futhan/EDTA controls in vitro complement activation. publication-title: Clin Chem – volume: 29 start-page: 1085 year: 1986 article-title: Complement activation during systemic lupus erythematosus. C3a and C5a anaphylatoxins circulate during exacerbations of disease. publication-title: Arthritis Rheum – volume: 1 start-page: 1764 year: 2003 article-title: Autoimmune antiphospholipid antibodies impair the inhibition of activated factor X by protein Z/protein Z-dependent protease inhibitor. publication-title: J Thromb Haemost – volume: 43 start-page: 1982 year: 2000 article-title: Association of autoantibodies against the phosphatidylserine-prothrombin complex with manifestations of the antiphospholipid syndrome and with the presence of lupus anticoagulant. publication-title: Arthritis Rheum – volume: 160 start-page: 5572 year: 1998 article-title: Human beta 2-glycoprotein I binds to endothelial cells through a cluster of lysine residues that are critical for anionic phospholipid binding and offers epitopes for anti-beta 2-glycoprotein I antibodies. publication-title: J Immunol – volume: 207 start-page: 17 year: 2003 article-title: Atherogenic autoantigen: oxidized LDL complexes with beta2-glycoprotein I. publication-title: Immunobiology – volume: 174 start-page: 3041 year: 2005 article-title: Macrophages induce the inflammatory response in the pulmonary Arthus reaction through G alpha i2 activation that controls C5aR and Fc receptor cooperation. publication-title: J Immunol – volume: 119 start-page: 781 year: 2002 article-title: Suppressed intrinsic fibrinolytic activity by monoclonal anti-beta-2 glycoprotein I autoantibodies: possible mechanism for thrombosis in patients with antiphospholipid syndrome. publication-title: Br J Haematol – volume: 16 start-page: 1633 year: 2004 article-title: The p38 mitogen-activated protein kinase (MAPK) pathway mediates induction of the tissue factor gene in monocytes stimulated with human monoclonal anti-beta2 glycoprotein I antibodies. publication-title: Int Immunol – volume: 24 start-page: 764 year: 1983 article-title: Anaphylatoxin formation during hemodialysis: effects of different dialyzer membranes. publication-title: Kidney Int – volume: 344 start-page: 1058 year: 2001 article-title: Complement. First of two parts. publication-title: N Engl J Med – volume: 17 start-page: 151 year: 1980 article-title: Human C5a and C5a analogs as probes of the neutrophil C5a receptor. publication-title: Mol Immunol – volume: 32 start-page: 259 year: 1989 article-title: Reduced numbers of complement receptor type 1 on erythrocytes are associated with increased levels of anticardiolipin antibodies. Findings in patients with systemic lupus erythematosus and the antiphospholipid syndrome. publication-title: Arthritis Rheum – volume: 17 start-page: 239 year: 2005 article-title: Normal pregnancy is characterized by systemic activation of the complement system. publication-title: J Matern Fetal Neonatal Med – volume: 104 start-page: 2353 year: 2004 article-title: Characterization of monocyte tissue factor activity induced by IgG antiphospholipid antibodies and inhibition by dilazep. publication-title: Blood – volume: 40 start-page: 1725 year: 1997 article-title: Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. publication-title: Arthritis Rheum – volume: 374 start-page: 33 year: 2006 article-title: Complement mediators in ischemia-reperfusion injury. publication-title: Clin Chim Acta – volume: 101 start-page: 3495 year: 2003 article-title: Role of the MyD88 transduction signaling pathway in endothelial activation by antiphospholipid antibodies. publication-title: Blood – volume: 124 start-page: 311 year: 2007 publication-title: Clin Immunol – volume: 160 start-page: 5572 year: 1998 ident: 10.1136/ard.2008.090670_bib5 article-title: Human beta 2-glycoprotein I binds to endothelial cells through a cluster of lysine residues that are critical for anionic phospholipid binding and offers epitopes for anti-beta 2-glycoprotein I antibodies publication-title: J Immunol doi: 10.4049/jimmunol.160.11.5572 – volume: 344 start-page: 1058 year: 2001 ident: 10.1136/ard.2008.090670_bib14 article-title: Complement. First of two parts publication-title: N Engl J Med doi: 10.1056/NEJM200104053441406 – volume: 68 start-page: 215 year: 1987 ident: 10.1136/ard.2008.090670_bib24 article-title: Evaluation of the anti-cardiolipin antibody test: report of an international workshop held 4 April 1986 publication-title: Clin Exp Immunol – volume: 10 start-page: 1222 year: 2004 ident: 10.1136/ard.2008.090670_bib19 article-title: Heparin prevents antiphospholipid antibody-induced fetal loss by inhibiting complement activation publication-title: Nat Med doi: 10.1038/nm1121 – volume: 174 start-page: 3041 year: 2005 ident: 10.1136/ard.2008.090670_bib17 article-title: Macrophages induce the inflammatory response in the pulmonary Arthus reaction through G alpha i2 activation that controls C5aR and Fc receptor cooperation publication-title: J Immunol doi: 10.4049/jimmunol.174.5.3041 – volume: 42 start-page: 1309 year: 1999 ident: 10.1136/ard.2008.090670_bib21 article-title: International consensus statement on preliminary classification criteria for definite antiphospholipid syndrome: report of an international workshop publication-title: Arthritis Rheum doi: 10.1002/1529-0131(199907)42:7<1309::AID-ANR1>3.0.CO;2-F – volume: 124 start-page: 311 year: 2007 ident: 10.1136/ard.2008.090670_bib34 publication-title: Clin Immunol doi: 10.1016/j.clim.2007.05.010 – volume: 16 start-page: 1633 year: 2004 ident: 10.1136/ard.2008.090670_bib4 article-title: The p38 mitogen-activated protein kinase (MAPK) pathway mediates induction of the tissue factor gene in monocytes stimulated with human monoclonal anti-beta2 glycoprotein I antibodies publication-title: Int Immunol doi: 10.1093/intimm/dxh166 – volume: 41 start-page: 1513 year: 1998 ident: 10.1136/ard.2008.090670_bib7 article-title: IgG2 restriction of anti-beta2-glycoprotein I as the basis for the association between IgG2 anticardiolipin antibodies and thrombosis in the antiphospholipid syndrome publication-title: Arthritis Rheum doi: 10.1002/1529-0131(199808)41:8<1513::AID-ART28>3.0.CO;2-7 – volume: 174 start-page: 485 year: 2005 ident: 10.1136/ard.2008.090670_bib41 article-title: TNF-alpha is a critical effector and a target for therapy in antiphospholipid antibody-induced pregnancy loss publication-title: J Immunol doi: 10.4049/jimmunol.174.1.485 – volume: 4 start-page: 295 year: 2006 ident: 10.1136/ard.2008.090670_bib1 article-title: International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS) publication-title: J Thromb Haemost doi: 10.1111/j.1538-7836.2006.01753.x – volume: 374 start-page: 33 year: 2006 ident: 10.1136/ard.2008.090670_bib33 article-title: Complement mediators in ischemia-reperfusion injury publication-title: Clin Chim Acta doi: 10.1016/j.cca.2006.06.010 – volume: 99 start-page: 1997 year: 1999 ident: 10.1136/ard.2008.090670_bib6 article-title: Antiphospholipid antibodies from antiphospholipid syndrome patients activate endothelial cells in vitro and in vivo publication-title: Circulation doi: 10.1161/01.CIR.99.15.1997 – volume: 177 start-page: 4794 year: 2006 ident: 10.1136/ard.2008.090670_bib32 article-title: A novel C5a receptor-tissue factor cross-talk in neutrophils links innate immunity to coagulation pathways publication-title: J Immunol doi: 10.4049/jimmunol.177.7.4794 – volume: 35 start-page: 1239 year: 1996 ident: 10.1136/ard.2008.090670_bib25 article-title: Specificity of ELISA for antibody to beta 2-glycoprotein I in patients with antiphospholipid syndrome publication-title: Br J Rheumatol doi: 10.1093/rheumatology/35.12.1239 – volume: 101 start-page: 3495 year: 2003 ident: 10.1136/ard.2008.090670_bib3 article-title: Role of the MyD88 transduction signaling pathway in endothelial activation by antiphospholipid antibodies publication-title: Blood doi: 10.1182/blood-2002-08-2349 – volume: 104 start-page: 2353 year: 2004 ident: 10.1136/ard.2008.090670_bib8 article-title: Characterization of monocyte tissue factor activity induced by IgG antiphospholipid antibodies and inhibition by dilazep publication-title: Blood doi: 10.1182/blood-2004-01-0145 – volume: 29 start-page: 1085 year: 1986 ident: 10.1136/ard.2008.090670_bib30 article-title: Complement activation during systemic lupus erythematosus. C3a and C5a anaphylatoxins circulate during exacerbations of disease publication-title: Arthritis Rheum doi: 10.1002/art.1780290905 – volume: 85 start-page: 198 year: 2001 ident: 10.1136/ard.2008.090670_bib40 article-title: Plasma tumor necrosis factor alpha levels and the −238*A promoter polymorphism in patients with antiphospholipid syndrome publication-title: Thromb Haemost doi: 10.1055/s-0037-1615676 – volume: 17 start-page: 239 year: 2005 ident: 10.1136/ard.2008.090670_bib31 article-title: Normal pregnancy is characterized by systemic activation of the complement system publication-title: J Matern Fetal Neonatal Med doi: 10.1080/14767050500072722 – volume: 207 start-page: 17 year: 2003 ident: 10.1136/ard.2008.090670_bib36 article-title: Atherogenic autoantigen: oxidized LDL complexes with beta2-glycoprotein I publication-title: Immunobiology doi: 10.1078/0171-2985-00214 – volume: 43 start-page: 1982 year: 2000 ident: 10.1136/ard.2008.090670_bib26 article-title: Association of autoantibodies against the phosphatidylserine-prothrombin complex with manifestations of the antiphospholipid syndrome and with the presence of lupus anticoagulant publication-title: Arthritis Rheum doi: 10.1002/1529-0131(200009)43:9<1982::AID-ANR9>3.0.CO;2-2 – volume: 40 start-page: 1026 year: 2001 ident: 10.1136/ard.2008.090670_bib38 article-title: IgG subclass distribution of antibodies against beta(2)-GP1 and cardiolipin in patients with systemic lupus erythematosus and primary antiphospholipid syndrome, and their clinical associations publication-title: Rheumatology (Oxford) doi: 10.1093/rheumatology/40.9.1026 – volume: 40 start-page: 1725 year: 1997 ident: 10.1136/ard.2008.090670_bib22 article-title: Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus publication-title: Arthritis Rheum doi: 10.1002/art.1780400928 – volume: 50 start-page: 2911 year: 2004 ident: 10.1136/ard.2008.090670_bib9 article-title: Intracellular events in platelet activation induced by antiphospholipid antibodies in the presence of low doses of thrombin publication-title: Arthritis Rheum doi: 10.1002/art.20434 – volume: 74 start-page: 1185 year: 1995 ident: 10.1136/ard.2008.090670_bib27 article-title: Criteria for the diagnosis of lupus anticoagulants: an update. On behalf of the Subcommittee on Lupus Anticoagulant/Antiphospholipid Antibody of the Scientific and Standardisation Committee of the ISTH publication-title: Thromb Haemost doi: 10.1055/s-0038-1649901 – volume: 42 start-page: 167 year: 1999 ident: 10.1136/ard.2008.090670_bib12 article-title: Beta2-glycoprotein I is necessary to inhibit protein C activity by monoclonal anticardiolipin antibodies publication-title: Arthritis Rheum doi: 10.1002/1529-0131(199901)42:1<167::AID-ANR20>3.0.CO;2-B – volume: 45 start-page: 1190 year: 1999 ident: 10.1136/ard.2008.090670_bib23 article-title: Possible mechanism for in vitro complement activation in blood and plasma samples: futhan/EDTA controls in vitro complement activation publication-title: Clin Chem doi: 10.1093/clinchem/45.8.1190 – volume: 158 start-page: 603 year: 1983 ident: 10.1136/ard.2008.090670_bib15 article-title: Human platelet activation by C3a and C3a des-Arg publication-title: J Exp Med doi: 10.1084/jem.158.2.603 – volume: 4 start-page: 2035 year: 2006 ident: 10.1136/ard.2008.090670_bib35 article-title: Blood platelets activate the classical pathway of human complement publication-title: J Thromb Haemost doi: 10.1111/j.1538-7836.2006.02065.x – volume: 1 start-page: 1764 year: 2003 ident: 10.1136/ard.2008.090670_bib13 article-title: Autoimmune antiphospholipid antibodies impair the inhibition of activated factor X by protein Z/protein Z-dependent protease inhibitor publication-title: J Thromb Haemost doi: 10.1046/j.1538-7836.2003.00303.x – volume: 17 start-page: 151 year: 1980 ident: 10.1136/ard.2008.090670_bib16 article-title: Human C5a and C5a analogs as probes of the neutrophil C5a receptor publication-title: Mol Immunol doi: 10.1016/0161-5890(80)90067-X – volume: 32 start-page: 259 year: 1989 ident: 10.1136/ard.2008.090670_bib39 article-title: Reduced numbers of complement receptor type 1 on erythrocytes are associated with increased levels of anticardiolipin antibodies. Findings in patients with systemic lupus erythematosus and the antiphospholipid syndrome publication-title: Arthritis Rheum doi: 10.1002/anr.1780320305 – volume: 112 start-page: 1644 year: 2003 ident: 10.1136/ard.2008.090670_bib18 article-title: Complement C5a receptors and neutrophils mediate fetal injury in the antiphospholipid syndrome publication-title: J Clin Invest doi: 10.1172/JCI200318817 – volume: 90 start-page: 434 year: 1992 ident: 10.1136/ard.2008.090670_bib37 article-title: Immunoglobulin class and IgG subclass distribution of antiphospholipid antibodies in patients with systemic lupus erythematosus and associated disorders publication-title: Clin Exp Immunol doi: 10.1111/j.1365-2249.1992.tb05864.x – start-page: 1081 year: 2004 ident: 10.1136/ard.2008.090670_bib2 article-title: Immunology of antiphospholipid antibodies and co-factors doi: 10.1016/B9-78-012433-9/01950-0429 – volume: 3 start-page: 140 year: 2007 ident: 10.1136/ard.2008.090670_bib20 article-title: The antiphospholipid syndrome as a disorder initiated by inflammation: implications for the therapy of pregnant patients publication-title: Nat Clin Pract Rheumatol doi: 10.1038/ncprheum0432 – volume: 112 start-page: 325 year: 1998 ident: 10.1136/ard.2008.090670_bib11 article-title: Binding of anticardiolipin antibodies to protein C via beta2-glycoprotein I (beta2-GPI): a possible mechanism in the inhibitory effect of antiphospholipid antibodies on the protein C system publication-title: Clin Exp Immunol doi: 10.1046/j.1365-2249.1998.00582.x – volume: 24 start-page: 764 year: 1983 ident: 10.1136/ard.2008.090670_bib29 article-title: Anaphylatoxin formation during hemodialysis: effects of different dialyzer membranes publication-title: Kidney Int doi: 10.1038/ki.1983.225 – volume: 304 start-page: 497 year: 1981 ident: 10.1136/ard.2008.090670_bib28 article-title: Complement activation during cardiopulmonary bypass: evidence for generation of C3a and C5a anaphylatoxins publication-title: N Engl J Med doi: 10.1056/NEJM198102263040901 – volume: 119 start-page: 781 year: 2002 ident: 10.1136/ard.2008.090670_bib10 article-title: Suppressed intrinsic fibrinolytic activity by monoclonal anti-beta-2 glycoprotein I autoantibodies: possible mechanism for thrombosis in patients with antiphospholipid syndrome publication-title: Br J Haematol doi: 10.1046/j.1365-2141.2002.03928.x |
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Snippet | Objective:To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS).Methods:Thirty-six patients with... Objective: To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS). Methods: Thirty-six patients with... To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS). Thirty-six patients with primary APS, 42... To investigate the significance of complement activation in patients with primary antiphospholipid syndrome (APS).OBJECTIVETo investigate the significance of... |
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SubjectTerms | Adolescent Adult Aged Anticoagulants Antigen-Antibody Complex - analysis Antiphospholipid Syndrome - blood Antiphospholipid Syndrome - immunology Biological and medical sciences Blood Coagulation Blood platelets Case-Control Studies Complement Activation - immunology Complement C3 - analysis Complement C3a - analysis Complement C4 - analysis Complement C4a - analysis Connective Tissue Diseases - immunology Cross-Sectional Studies Disease Diseases of the osteoarticular system Female Humans Hypotheses Immunoglobulins Lupus Male Medical imaging Medical sciences Middle Aged NMR Nuclear magnetic resonance Plasma Pregnancy Retrospective Studies Statistics, Nonparametric Thrombosis Tumor Necrosis Factor-alpha - blood Tumor necrosis factor-TNF Young Adult |
Title | Complement activation in patients with primary antiphospholipid syndrome |
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