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

被引:15
作者
Badr, Gamal [1 ,2 ,3 ]
Sayed, Douaa [4 ]
Alhazza, Ibrahim M. [1 ,2 ]
Elsayh, Khalid I. [5 ]
Ahmed, Emad A. [3 ]
Alwasel, Saleh H. [1 ,2 ]
机构
[1] King Saud Univ, Coll Sci, Dept Zool, Riyadh 2455, Saudi Arabia
[2] King Saud Univ, Coll Sci, Fetal Programming Dis Res Chair, Riyadh 2455, Saudi Arabia
[3] Assiut Univ, Fac Sci, Dept Zool, Assiut, Egypt
[4] Assiut Univ, S Egypt Canc Inst, Dept Clin Pathol, Assiut, Egypt
[5] Assiut Univ, Fac Med, Dept Pediat, Assiut, Egypt
关键词
Apoptosis; Malnutrition; Infants; Flow cytometry; FLOW-CYTOMETRY; APOPTOSIS; FAS; EXPRESSION; CYTOKINES; CHILDREN; MICE; IL-7; MALNUTRITION; SUBSETS;
D O I
10.1016/j.imbio.2010.07.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 beta, IL-6, IL-10 and TNF-alpha, 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 Ala 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. (C) 2010 Elsevier GmbH. All rights reserved.
引用
收藏
页码:309 / 315
页数:7
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