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T lymphocytes from malnourished infants are short-lived and dysfunctional cells

Research Authors
Gamal Badr, Douaa Sayed, Ibrahim M. Alhazza, Khalid I. Elsayh, Emad A. Ahmed, Saleh H. Alwasel
Research Abstract

To investigate T-cell functional molecules and inflammatory cytokines and to assess T-cell apoptosis
in malnourished infants, 64 infants from undernourished women and 28 healthy control infants were
recruited to the study. Malnourished infants showed a significant decrease in the levels of circulating IL-2
and IL-7 and increases in the levels of IL-1, IL-6, IL-10 and TNF-, as measured by flow cytometry. There
was a significant reduction in the number of CD3+ T cells and an increase in apoptotic T cells, which was
associated with an up-regulation of CD95 and PD-1 expression on CD3+ T cells in malnourished compared
to control infants. Significant reductions were also observed in the phosphorylation of AKT and STAT5
and in the expression of CCR7 and CXCR4 receptors in malnourished children, and these reductions were
associated with a significant reduction in T-cell migratory capacity to their ligands CCL21 and CXCL12,
respectively, as measured using an in vitro chemotaxis assay. Taken together, these data suggest that
lymphocytes from malnourished infants are short-lived and dysfunctional.

Research Department
Research Journal
Immunobiology
Research Member
Research Rank
1
Research Vol
216(3):
Research Year
2011
Research Pages
PP.309–315