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The functional connotations of iron deficiency-effect on neutrophil oxidative burst activity in preschool children
Shweta Dutt1, Poonam Rani1, Richa Gupta1
1Department of Pathology, University College of Medical Sciences and Guru Teg Bahadur Hospital Delhi, India.
Insights
Iron deficiency anaemia impairs neutrophil oxidative burst, a key defense against bacterial infections. This study confirms reduced immune response in children with IDA, increasing infection susceptibility.
Area of Science:
- Immunology
- Hematology
- Pediatrics
Background:
- Iron deficiency anaemia (IDA) compromises the innate immune system, particularly neutrophil antimicrobial functions.
- Neutrophil oxidative burst, crucial for fighting bacterial infections, is iron-dependent.
- Previous studies on iron deficiency's impact on neutrophil function often used less precise methods like the Nitro blue tetrazolium test.
Purpose of the Study:
- To evaluate the effect of iron deficiency on neutrophil oxidative burst activity in children under 5 years.
- To compare neutrophil function in children with IDA to a control group using flow cytometry.
- To investigate the utility of the dihydro rhodamine (DHR) assay in assessing immune function in pediatric IDA.
Main Methods:
- A case-control study involving 36 children aged 6 months to 5 years with moderate to severe IDA and 36 matched controls.
- Analysis of hematological and iron profile parameters, including hemoglobin, serum vitamin B12, and folate levels.
- Assessment of neutrophil oxidative burst activity using the flow cytometry-based Dihydrorhodamine (DHR) assay.
Main Results:
- Significantly reduced neutrophil oxidative burst parameters (percentage of stimulated neutrophils, Mean Fluorescence Index, Neutrophil oxidative index) were observed in children with IDA compared to controls.
- Hemoglobin levels showed a significant positive correlation with neutrophil oxidative index and the percentage of neutrophils exhibiting stimulation in the IDA group.
- The DHR assay demonstrated a clear deficit in neutrophil function associated with iron deficiency.
Conclusions:
- Children with iron deficiency anaemia exhibit a significantly impaired neutrophil oxidative burst, indicating a weakened innate immune response.
- This diminished immune function increases susceptibility to bacterial infections, with severity correlating to the degree of anaemia.
- The findings highlight the critical role of iron in immune defense and the need for timely intervention in pediatric IDA.
Abstract:
Iron deficiency anaemia (IDA) makes an individual prone to bacterial infections. The antimicrobial defence mechanism of neutrophils is orchestrated by Nicotinamide Adenine Dinucleotide Phosphate Hydrogen (NADPH) oxidative burst which is iron-dependent. The few previous studies documenting a decrease in neutrophil oxidative burst in iron-deficient children have been based mainly on the Nitro blue tetrazolium test (NBT). Very few studies have been conducted using the more robust flow cytometry-based dihydro rhodamine (DHR) assay in this regard worldwide and none in India.
Aim:
To estimate the effect of iron deficiency on neutrophil oxidative burst activity in children under 5 years of age by flow cytometry-based dihydro rhodamine (DHR) assay and compare it with the control group.
Methods:
Thirty-six children between 6 months to 5 years of age diagnosed with moderate (Hb 7-10 gm/dl) to severe (Hb <7 gm/dl) iron deficiency anaemia were selected as cases with equal number of sex/age matched controls. The peripheral blood was analyzed for hematological and biochemical parameters such as complete iron profile, serum vitamin B12, and folate levels. The oxidative burst activity of neutrophils in peripheral blood was assessed using a flow-cytometry-based Dihydrorhodamine (DHR) assay.
Results:
The percentage of neutrophils showing stimulation, Mean Fluorescence Index in stimulated neutrophils, and Neutrophil oxidative index (NOI) were significantly reduced in iron deficiency anaemia patients as compared to controls. In cases, haemoglobin showed significant positive correlation with NOI and percentage of neutrophils showing stimulation.
Conclusion:
To conclude, a significant decrease in neutrophil oxidative burst parameters depicts an insufficient innate immune response to pathogens and makes Iron deficiency anaemia patients more susceptible to infections, further aggravated by the severity of anaemia.
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