Evaluation of the Serum Levels of Immunoglobulin and Complement Factors in b-thalassemia Major Patients in Southern Iran

Authors

  • Ahmad Amin Hematology Research Center, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
  • Mehran Karimi Hematology Research Center, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
  • Nima Jamalian Hematology Research Center, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
  • Reza Amin Department of Pediatrics, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
  • Soheila Aale-yasin Department of Pediatrics, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
  • Susan Jalali Hematology Research Center, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran
Abstract:

Background: Beta-thalassemia major is one of the major health problems in our country. Many studies have confirmed the fact that, these patients have an increased susceptibility to bacterial infections. Objective: In this study, we have assessed the humoral immune system in 68 thalassemic patients by measuring their serum concentration of Immunoglobulin G (IgG), IgM, IgA, C3 and C4 in order to find out a responsible immune defect. Methods: Sixty eight b-thalassemia major patients were enrolled randomly from referrals to Dastgheib clinic of thalassemia. The same number of case controls with matched age and sex were selected from healthy people without any history of recent or recurrent infections. Serum IgG, IgM, IgA, C3 and C4 levels were assessed using Single Radial Immunodiffusion (SRID). Results: Serum levels of IgG, IgM & IgA were significantly higher (P

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evaluation of the serum levels of immunoglobulin and complement factors in b-thalassemia major patients in southern iran

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Journal title

volume 2  issue 4

pages  220- 225

publication date 2005-12-01

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