Humeral immune system state in β thalassemia major

被引:0
作者
Ghaffari, Javad [2 ]
Vahidshahi, Koorosh
Kosaryan, Mehrnoosh [1 ]
Soffantooyeh, Zahra
Mohamadi, Mohadese
机构
[1] Mazandaran Univ Med Sci, Dept Pediat, Div Endocrinol, Thalassemia Res Ctr, Babol Sar, Iran
[2] Mazandaran Univ Med Sci, Dept Pediat, Div Immunol & Allergy, Sari, Iran
关键词
major beta-thalassemia; serum immunoglobulins; serum complements; isohemaglutinin; ASO; IMMUNOLOGICAL EVALUATION; COMPLEMENT;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim To investigate the humeral immune markers in patients with beta-thalassemia major (TM). Methods In this historical - cohort study (August to December 2007), the case group consisted of 34 TM patients and the control group included the same number of their gender and age matched healthy siblings. Serum levels of CH50, C3, C4, IgE, IgG,IgA,IgM and also ASO & Isohemaglutinin titers were determined and compared between the case and control groups (P<0.05). Results Serum level of IgA in TM patients was more frequently higher than normal level compared to the controls, but there were no significant differences on the level of C3, C4, CH50, IgG, IgE, IgM, ASO and Isohemaglutinin between two groups. Splenectomized patients had lower IgM and higher IgA and IgG levels and also diabetic patients had significantly lower C3, ASO, IgM and higher IgA and IgG levels than other patients. Levels of IgA, IgE, IgG, and ASO increased in elder patients. Patients with serum ferritin level >3000ng/ml had lower C4 and CH50 levels. C4-level in male patients was significantly lower. Conclusion This study indicated that there were no significant changes in humeral immune markers in the patients with beta-thalassemia major compared to the controls, except in the case of IgA which was higher in the TM patients. It seems that there is no need for routine survey of immunoglobulins and complement levels in thalassemic patients in order to detect immunodeficiency.
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页码:192 / 196
页数:5
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