Complement activation in patients with immune thrombocytopenic purpura according to phases of disease course
Summary Immune thrombocytopenic purpura (ITP) is an autoimmune thrombocytopenia with shortened platelet survival and relative bone marrow failure. The pathogenesis involves antibody production, cytokine release, T cell impairment, complement activation and clearance of platelets. We measured plasma...
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Published in | Clinical and experimental immunology Vol. 201; no. 3; pp. 258 - 265 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
England
Oxford University Press
01.09.2020
John Wiley and Sons Inc |
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Online Access | Get full text |
ISSN | 0009-9104 1365-2249 1365-2249 |
DOI | 10.1111/cei.13475 |
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Abstract | Summary
Immune thrombocytopenic purpura (ITP) is an autoimmune thrombocytopenia with shortened platelet survival and relative bone marrow failure. The pathogenesis involves antibody production, cytokine release, T cell impairment, complement activation and clearance of platelets. We measured plasma levels of C3, C4, C1q and sC5b‐9 in 80 ITP patients in acute phase, 50 ITP patients in complete (CR) or partial (PR) remission and 50 age‐ and sex‐matched healthy volunteers. Statistical analyses showed that acute ITP patients had higher plasma levels of sC5b‐9 and C1q than CR or PR patients (median = sC5b‐9: 200 versus 98 mg/dl, P‐value < 0·001) (median C1q = 2·11 versus 1·00 mg/dl, P‐value < 0·001). CR and PR ITP patients had sC5b‐9 and C1q plasma levels comparable to those observed in healthy volunteers. There was a significant correlation between sC5b‐9 and C1q plasma levels (Spearman’s rho correlation index on 130 ITP patients equal to 0·58, P‐value < 0·001). We also found that sC5b‐9 plasma level is inversely correlated with the number of platelets. Furthermore, we divided acute ITP patients into subjects with detectable (24 of 80, 30%) or undetectable (56 of 80, 70%) anti‐platelet antibodies; patients with detectable anti‐platelet antibodies have significantly higher plasma levels of C1q and sC5b‐9. This research will potentially offer novel therapeutic strategies in light of new drugs affecting complement activation for monitoring therapy response.
Immune Thrombocytopenic Purpura (ITP) is an autoimmune thrombocytopenia with a shortened platelet survival and relative bone marrow failure. We measured plasma levels of C3, C4, C1q, sC5b‐9 in 80 ITP patients in acute phase, 50 ITP patients in complete (CR) or partial (PR) remission, and 50 age‐ and sex‐matched healthy volunteers. Statistical analyses showed that acute ITP patients had higher plasma levels of sC5b‐9 and C1q than CR or PR patients We also found that sC5b‐9 plasma level is inversely correlated with the number of platelets. |
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AbstractList | Immune thrombocytopenic purpura (ITP) is an autoimmune thrombocytopenia with shortened platelet survival and relative bone marrow failure. The pathogenesis involves antibody production, cytokine release, T cell impairment, complement activation and clearance of platelets. We measured plasma levels of C3, C4, C1q and sC5b‐9 in 80 ITP patients in acute phase, 50 ITP patients in complete (CR) or partial (PR) remission and 50 age‐ and sex‐matched healthy volunteers. Statistical analyses showed that acute ITP patients had higher plasma levels of sC5b‐9 and C1q than CR or PR patients (median = sC5b‐9: 200
versus
98 mg/dl,
P
‐value < 0·001) (median C1q = 2·11
versus
1·00 mg/dl,
P
‐value < 0·001). CR and PR ITP patients had sC5b‐9 and C1q plasma levels comparable to those observed in healthy volunteers. There was a significant correlation between sC5b‐9 and C1q plasma levels (Spearman’s rho correlation index on 130 ITP patients equal to 0·58,
P
‐value < 0·001). We also found that sC5b‐9 plasma level is inversely correlated with the number of platelets. Furthermore, we divided acute ITP patients into subjects with detectable (24 of 80, 30%) or undetectable (56 of 80, 70%) anti‐platelet antibodies; patients with detectable anti‐platelet antibodies have significantly higher plasma levels of C1q and sC5b‐9. This research will potentially offer novel therapeutic strategies in light of new drugs affecting complement activation for monitoring therapy response.
Immune Thrombocytopenic Purpura (ITP) is an autoimmune thrombocytopenia with a shortened platelet survival and relative bone marrow failure. We measured plasma levels of C3, C4, C1q, sC5b‐9 in 80 ITP patients in acute phase, 50 ITP patients in complete (CR) or partial (PR) remission, and 50 age‐ and sex‐matched healthy volunteers. Statistical analyses showed that acute ITP patients had higher plasma levels of sC5b‐9 and C1q than CR or PR patients We also found that sC5b‐9 plasma level is inversely correlated with the number of platelets. Immune thrombocytopenic purpura (ITP) is an autoimmune thrombocytopenia with shortened platelet survival and relative bone marrow failure. The pathogenesis involves antibody production, cytokine release, T cell impairment, complement activation and clearance of platelets. We measured plasma levels of C3, C4, C1q and sC5b-9 in 80 ITP patients in acute phase, 50 ITP patients in complete (CR) or partial (PR) remission and 50 age- and sex-matched healthy volunteers. Statistical analyses showed that acute ITP patients had higher plasma levels of sC5b-9 and C1q than CR or PR patients (median = sC5b-9: 200 versus 98 mg/dl, P-value < 0·001) (median C1q = 2·11 versus 1·00 mg/dl, P-value < 0·001). CR and PR ITP patients had sC5b-9 and C1q plasma levels comparable to those observed in healthy volunteers. There was a significant correlation between sC5b-9 and C1q plasma levels (Spearman's rho correlation index on 130 ITP patients equal to 0·58, P-value < 0·001). We also found that sC5b-9 plasma level is inversely correlated with the number of platelets. Furthermore, we divided acute ITP patients into subjects with detectable (24 of 80, 30%) or undetectable (56 of 80, 70%) anti-platelet antibodies; patients with detectable anti-platelet antibodies have significantly higher plasma levels of C1q and sC5b-9. This research will potentially offer novel therapeutic strategies in light of new drugs affecting complement activation for monitoring therapy response.Immune thrombocytopenic purpura (ITP) is an autoimmune thrombocytopenia with shortened platelet survival and relative bone marrow failure. The pathogenesis involves antibody production, cytokine release, T cell impairment, complement activation and clearance of platelets. We measured plasma levels of C3, C4, C1q and sC5b-9 in 80 ITP patients in acute phase, 50 ITP patients in complete (CR) or partial (PR) remission and 50 age- and sex-matched healthy volunteers. Statistical analyses showed that acute ITP patients had higher plasma levels of sC5b-9 and C1q than CR or PR patients (median = sC5b-9: 200 versus 98 mg/dl, P-value < 0·001) (median C1q = 2·11 versus 1·00 mg/dl, P-value < 0·001). CR and PR ITP patients had sC5b-9 and C1q plasma levels comparable to those observed in healthy volunteers. There was a significant correlation between sC5b-9 and C1q plasma levels (Spearman's rho correlation index on 130 ITP patients equal to 0·58, P-value < 0·001). We also found that sC5b-9 plasma level is inversely correlated with the number of platelets. Furthermore, we divided acute ITP patients into subjects with detectable (24 of 80, 30%) or undetectable (56 of 80, 70%) anti-platelet antibodies; patients with detectable anti-platelet antibodies have significantly higher plasma levels of C1q and sC5b-9. This research will potentially offer novel therapeutic strategies in light of new drugs affecting complement activation for monitoring therapy response. Immune thrombocytopenic purpura (ITP) is an autoimmune thrombocytopenia with shortened platelet survival and relative bone marrow failure. The pathogenesis involves antibody production, cytokine release, T cell impairment, complement activation and clearance of platelets. We measured plasma levels of C3, C4, C1q and sC5b-9 in 80 ITP patients in acute phase, 50 ITP patients in complete (CR) or partial (PR) remission and 50 age- and sex-matched healthy volunteers. Statistical analyses showed that acute ITP patients had higher plasma levels of sC5b-9 and C1q than CR or PR patients (median = sC5b-9: 200 versus 98 mg/dl, P-value < 0·001) (median C1q = 2·11 versus 1·00 mg/dl, P-value < 0·001). CR and PR ITP patients had sC5b-9 and C1q plasma levels comparable to those observed in healthy volunteers. There was a significant correlation between sC5b-9 and C1q plasma levels (Spearman's rho correlation index on 130 ITP patients equal to 0·58, P-value < 0·001). We also found that sC5b-9 plasma level is inversely correlated with the number of platelets. Furthermore, we divided acute ITP patients into subjects with detectable (24 of 80, 30%) or undetectable (56 of 80, 70%) anti-platelet antibodies; patients with detectable anti-platelet antibodies have significantly higher plasma levels of C1q and sC5b-9. This research will potentially offer novel therapeutic strategies in light of new drugs affecting complement activation for monitoring therapy response. Immune thrombocytopenic purpura (ITP) is an autoimmune thrombocytopenia with shortened platelet survival and relative bone marrow failure. The pathogenesis involves antibody production, cytokine release, T cell impairment, complement activation and clearance of platelets. We measured plasma levels of C3, C4, C1q and sC5b‐9 in 80 ITP patients in acute phase, 50 ITP patients in complete (CR) or partial (PR) remission and 50 age‐ and sex‐matched healthy volunteers. Statistical analyses showed that acute ITP patients had higher plasma levels of sC5b‐9 and C1q than CR or PR patients (median = sC5b‐9: 200 versus 98 mg/dl, P‐value < 0·001) (median C1q = 2·11 versus 1·00 mg/dl, P‐value < 0·001). CR and PR ITP patients had sC5b‐9 and C1q plasma levels comparable to those observed in healthy volunteers. There was a significant correlation between sC5b‐9 and C1q plasma levels (Spearman’s rho correlation index on 130 ITP patients equal to 0·58, P‐value < 0·001). We also found that sC5b‐9 plasma level is inversely correlated with the number of platelets. Furthermore, we divided acute ITP patients into subjects with detectable (24 of 80, 30%) or undetectable (56 of 80, 70%) anti‐platelet antibodies; patients with detectable anti‐platelet antibodies have significantly higher plasma levels of C1q and sC5b‐9. This research will potentially offer novel therapeutic strategies in light of new drugs affecting complement activation for monitoring therapy response. Summary Immune thrombocytopenic purpura (ITP) is an autoimmune thrombocytopenia with shortened platelet survival and relative bone marrow failure. The pathogenesis involves antibody production, cytokine release, T cell impairment, complement activation and clearance of platelets. We measured plasma levels of C3, C4, C1q and sC5b‐9 in 80 ITP patients in acute phase, 50 ITP patients in complete (CR) or partial (PR) remission and 50 age‐ and sex‐matched healthy volunteers. Statistical analyses showed that acute ITP patients had higher plasma levels of sC5b‐9 and C1q than CR or PR patients (median = sC5b‐9: 200 versus 98 mg/dl, P‐value < 0·001) (median C1q = 2·11 versus 1·00 mg/dl, P‐value < 0·001). CR and PR ITP patients had sC5b‐9 and C1q plasma levels comparable to those observed in healthy volunteers. There was a significant correlation between sC5b‐9 and C1q plasma levels (Spearman’s rho correlation index on 130 ITP patients equal to 0·58, P‐value < 0·001). We also found that sC5b‐9 plasma level is inversely correlated with the number of platelets. Furthermore, we divided acute ITP patients into subjects with detectable (24 of 80, 30%) or undetectable (56 of 80, 70%) anti‐platelet antibodies; patients with detectable anti‐platelet antibodies have significantly higher plasma levels of C1q and sC5b‐9. This research will potentially offer novel therapeutic strategies in light of new drugs affecting complement activation for monitoring therapy response. Immune Thrombocytopenic Purpura (ITP) is an autoimmune thrombocytopenia with a shortened platelet survival and relative bone marrow failure. We measured plasma levels of C3, C4, C1q, sC5b‐9 in 80 ITP patients in acute phase, 50 ITP patients in complete (CR) or partial (PR) remission, and 50 age‐ and sex‐matched healthy volunteers. Statistical analyses showed that acute ITP patients had higher plasma levels of sC5b‐9 and C1q than CR or PR patients We also found that sC5b‐9 plasma level is inversely correlated with the number of platelets. |
Author | Lambertenghi Delilliers, G. Cicardi, M. Castelli, R. Gidaro, A. Bergamaschini, L. |
AuthorAffiliation | 1 Department of Biomedical and Clinical Sciences Luigi Sacco University of Milan Luigi Sacco Hospital Milan Italy 2 Fondazione Mattarelli Milan Italy |
AuthorAffiliation_xml | – name: 2 Fondazione Mattarelli Milan Italy – name: 1 Department of Biomedical and Clinical Sciences Luigi Sacco University of Milan Luigi Sacco Hospital Milan Italy |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/32515487$$D View this record in MEDLINE/PubMed |
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Keywords | C1q ITP immunoglobulin Anti-platelet antibody thrombocytopenia complement system sC5b-9 |
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Immune thrombocytopenic purpura (ITP) is an autoimmune thrombocytopenia with shortened platelet survival and relative bone marrow failure. The... Immune thrombocytopenic purpura (ITP) is an autoimmune thrombocytopenia with shortened platelet survival and relative bone marrow failure. The pathogenesis... |
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SubjectTerms | Adolescent Adult Antibodies Anti‐platelet antibody Autoantibodies - immunology Blood Platelets - immunology Bone marrow C1q Cell activation Complement activation Complement Activation - immunology Complement component C1q Complement component C3 Complement component C4 complement system Complement System Proteins - metabolism Disease Progression Female Humans Immune clearance immunoglobulin Immunosuppressive agents ITP Lymphocytes T Male Middle Aged Original Plasma Plasma levels Platelets Purpura Purpura, Thrombocytopenic, Idiopathic - immunology Remission sC5b‐9 Statistical analysis Thrombocytopenia Thrombocytopenic purpura Young Adult |
Title | Complement activation in patients with immune thrombocytopenic purpura according to phases of disease course |
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