Humoral and Complement Systems in Children With Acute Immune Thrombocytopenic Purpura

• Main Authors: Hossein Karami (Author), Javad Ghaffari (Author), Siavash Moradi (Author), Laleh Vahedi (Author), Fatemeh Mohammadi-Kharkeshi (Author)
• Format: Book
• Published: Mazandaran University of Medical Sciences, 2020-04-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.
• Notes: 2322-4398; 2322-4401
• Keywords: immune thrombocytopenia; humeral immunity; complements system; children; Pediatrics; RJ1-570
• Source: Journal of Pediatrics Review, Vol 8, Iss 2, Pp 133-138 (2020)

Background: Immune thrombocytopenia (ITP) is an autoimmune disorder associated with decreased platelet production and accelerated platelet destruction. An impaired immune system may induce by or be associated with ITP. Objectives: This study aimed to evaluate complement and humoral immune systems in ITP. Methods: We evaluated 30 children (under 19 years old) with acute and chronic ITP referred to a tertiary hospital and compared them with 30 healthy volunteers. We assessed the samples' CBC with differentiation, serum immunoglobulins (IgG, IgE, IgM, IgA, IgG1, IgG2, IgG3, IgG4) by nephelometry, antistreptolysin O titer by agglutination, CH50, C3, C4 by nephelometry, CD19 by flow cytometry, and anti-tetanus antibody titer by ELISA. Their demographic data were obtained with a questionnaire. Results: Our findings showed that humoral and complement components were normal in both patients and healthy groups. However, based on independent t test results, the mean serum levels of IgM, IgE, IgG1, C3, and tetanus antibody levels were significantly higher in the patient group. Conclusions: Humoral and complementary immunodeficiency in these patients is unlikely. However, more studies with larger sample sizes are needed.