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 inClinical and experimental immunology Vol. 201; no. 3; pp. 258 - 265
Main Authors Castelli, R., Lambertenghi Delilliers, G., Gidaro, A., Cicardi, M., Bergamaschini, L.
Format Journal Article
LanguageEnglish
Published England Oxford University Press 01.09.2020
John Wiley and Sons Inc
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Online AccessGet full text
ISSN0009-9104
1365-2249
1365-2249
DOI10.1111/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.
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
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Keywords C1q
ITP
immunoglobulin
Anti-platelet antibody
thrombocytopenia
complement system
sC5b-9
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Snippet Summary 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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StartPage 258
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
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fcei.13475
https://www.ncbi.nlm.nih.gov/pubmed/32515487
https://www.proquest.com/docview/2432756432
https://www.proquest.com/docview/2411104783
https://pubmed.ncbi.nlm.nih.gov/PMC7419927
Volume 201
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