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Complement activation in patients with immune thrombocytopenic purpura according to phases of disease course
- Source :
- Clin Exp Immunol
- Publication Year :
- 2020
- Publisher :
- Oxford University Press (OUP), 2020.
-
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
- Subjects :
- Adult
Blood Platelets
Male
0301 basic medicine
Adolescent
medicine.medical_treatment
Immunology
Pathogenesis
Young Adult
03 medical and health sciences
0302 clinical medicine
Immune system
immune system diseases
hemic and lymphatic diseases
medicine
Humans
Immunology and Allergy
Platelet
Complement Activation
Autoantibodies
Purpura, Thrombocytopenic, Idiopathic
biology
business.industry
Bone marrow failure
Complement System Proteins
Original Articles
Middle Aged
medicine.disease
Thrombocytopenic purpura
Complement system
030104 developmental biology
Cytokine
Disease Progression
biology.protein
Female
Antibody
business
030215 immunology
Subjects
Details
- ISSN :
- 13652249 and 00099104
- Volume :
- 201
- Database :
- OpenAIRE
- Journal :
- Clinical and Experimental Immunology
- Accession number :
- edsair.doi.dedup.....f4fb1d8d73502b3e028ce28e69a3062c