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Impact of iron deficiency anaemia on T lymphocytes & their subsets in children
Shalini Mullick1, Usha Rusia, Meera Sikka
1Department of Pathology, St John's Medical College, Bangalore, India.
Insights
Iron deficiency in children significantly alters T cell subsets, impacting immune function. Oral iron supplementation can improve these immune cell counts, highlighting iron's crucial role in pediatric immunity.
Area of Science:
- Pediatric Immunology
- Nutritional Immunology
- Hematology
Background:
- Iron deficiency (ID) is common in children and linked to altered immune profiles, but its specific immunoregulatory role remains unclear.
- Limited data exists on the impact of iron deficiency on T cell subsets in young children, a vulnerable population.
- Understanding iron's effect on immunity is crucial for addressing the global burden of micronutrient deficiencies.
Purpose of the Study:
- To document changes in T cell subsets (T lymphocytes, CD4+, CD8+, CD4:CD8 ratio) in children aged 1-5 years with iron deficiency.
- To investigate the impact of oral iron supplementation on these T cell parameters in iron-deficient children.
Main Methods:
- Comparative analysis of T lymphocyte subsets (CD4+, CD8+) and CD4:CD8 ratio in 40 iron-deficient children and 30 healthy controls.
- Evaluation of the effects of three months of oral iron supplementation on T cell parameters in 30 iron-deficient children.
Main Results:
- Iron-deficient children exhibited significantly lower levels of T lymphocytes (P<0.01) and CD4+ cells (P<0.002).
- A significantly lower CD4:CD8 ratio was observed in iron-deficient children (P<0.05).
- Oral iron supplementation led to a significant improvement in CD4+ cell counts.
Conclusions:
- Iron deficiency in children is quantitatively associated with altered T cell subsets, affecting immune status.
- A correlation exists between the severity of hematological and immunological compromise in iron deficiency.
- These findings underscore the clinical and epidemiological significance of addressing iron deficiency, the most prevalent micronutrient deficiency globally.
Background & Objectives:
While there is evidence of an altered immune profile in iron deficiency, the precise immunoregulatory role of iron is not known. Information particular in children who are vulnerable to iron deficiency and infection, is lacking. We undertook this study with the aim of documenting the changes in T cell subsets in children in the age group of 1 to 5 yr with iron deficiency.
Methods:
The levels of T lymphocytes, their CD4+ and CD8+ subsets and the CD4 : CD8 ratio were evaluated in 40 iron deficient and 30 healthy children. The impact of oral iron supplementation for three months on the same parameters was also noted in 30 children.
Results:
Significantly lower levels of T lymphocytes as well as CD4+ cells was observed in the iron deficient children (P<0.01 and 0.002 respectively). The CD4 : CD8 ratio was also significantly lower in this group (P<0.05). Iron supplementation improved the CD4 counts significantly.
Interpretation & Conclusion:
Our study demonstrated quantitatively altered T cell subsets in iron deficiency in children, and a relationship between the severity of haematological and immunological compromise. The clinical and epidemiological implications of this relationship have topical relevance since ID is the most common micronutrient deficiency worldwide.
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