الفهرس 
ThalassemiaOnly 14 pages are availabe for public view
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Abstract
Background: β-thalassemia is a major public health problem in Egypt with particularly high incidence due to strong cultural preference for consanguineous marriages, and the high carrier rate. Iron overload, which is caused by increased gut iron absorption secondary to ineffective erythropoiesis, and regular blood transfusion is linked to accumulation within different organs with subsequent organ dysfunction. Monocytes are important lineages of innate immunity which activate the adaptive immune response and play a pivotal role in the host response to pathogens. Human blood monocyte subsets classification is based on the expression of CD14 and CD16 cell surface receptors.
Aim of the Work: To evaluate the circulating monocyte subsets in β-thalassemia major (β-TM) patients and its potential role in prediction of iron overload and chronic inflammation in β-thalassemia major patients.
Patients and Methods: A Case-Control study conducted on 40 previously diagnosed beta thalassemia major patients attending the outpatient clinic of Ain Shams University Pediatric Hospital, and 20 age and sex matched healthy control subjects. CBC, iron profile, CRP and immunophenotyping for monocyte subsets classification were done.
Results: Non classical monocytes were found statistically significantly higher in thalassemic patients especially in those with serum ferritin level < 1000 ng/ml (P value < 0.01). In addition, classical monocytes were found to be statistically significantly lower among the patients’ group (P value < 0.01). A negative correlation was found between intermediate monocytes and Transferrin saturation percent (TS%) suggesting its protective role in iron overload thalassemia patients. By using ROC curve, non-classical monocytes predicted ferritin < 1000 ng/ml at a cutoff point of 17.8 % and 0.05 x 10^9/L for relative and absolute counts respectively.
Conclusion: All monocyte subsets proposed to have role in predicting iron overload and chronic inflammation β-TM patients. We recommend further studies on β-TM patients with the engagement of activity assays of monocyte subsets to clarify the co-regulatory role in iron hemostasis and chronic inflammation.