The influence of processing factors and non-atopy-related maternal and neonate characteristics on yield and cytokine responses of cord blood mononuclear cells

被引:23
作者
Dillie, K. T. Sullivan [1 ]
Tisler, C. J. [1 ]
DaSilva, D. F. [1 ]
Pappas, T. E. [1 ]
Roberg, K. A. [1 ]
Carlson-Dakes, K. T. [1 ]
Evans, M. D. [2 ]
Rosenthal, L. A. [3 ]
Gangnon, R. E. [2 ]
Gern, J. E. [1 ]
Lemanske, F., Jr. [1 ,3 ]
机构
[1] Univ Wisconsin, Dept Pediat, Madison, WI 53792 USA
[2] Univ Wisconsin, Dept Biostat & Med Informat, Madison, WI 53792 USA
[3] Univ Wisconsin, Dept Med, Madison, WI 53792 USA
关键词
cord blood; environmental exposures; interleukins; mononuclear cells; season of year;
D O I
10.1111/j.1365-2222.2007.02891.x
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
Rationale Several studies have evaluated the associations between cord blood cellular responses and atopic diseases in children, but the results of these studies are inconsistent. Variations in blood processing factors and maternal and infant characteristics are typically not accounted for and may contribute to these inconsistencies. Methods Cord blood samples were obtained from 287 subjects participating in the Childhood Origins of ASThma project, a prospective study of children at high risk for the development of asthma/allergies. Mononuclear cells were stimulated with phytohaemagglutinin (PHA), phorbal myristate acetate/ionomycin or a suspension of killed staphylococcus, and IFN-gamma, IL-10 and IL-13 were quantitated by ELISA. Cell yields and cytokine production were related to processing factors and maternal and infant characteristics. Results The strongest relationships between independent variables and cell yield or cytokine responses occurred with the season of birth. The highest median cell yields were seen in fall, and the lowest in summer (difference of 47%, P=0.0027). Furthermore, PHA-induced IL-5 and IL-13 responses were approximately 50% higher in spring and summer than in fall or winter (P < 0.0001). Clots in the cord blood samples were associated with a reduced median cell yield (42% reduction, P < 0.0001), and an increased PHA-induced IL-10 secretion (27% increase, P=0.004). Conclusions These data suggest that season of collection, and to a lesser extent clotting in samples, affect cord blood mononuclear cell yield and cytokine responses. Careful documentation and analysis of processing and environmental variables are important in understanding biological relationships with cytokine responses, and also lead to greater comparability among studies using these techniques.
引用
收藏
页码:298 / 304
页数:7
相关论文
共 27 条
[1]   DETERMINANTS OF CORD-BLOOD IGE CONCENTRATIONS IN 6401 GERMAN NEONATES [J].
BERGMANN, RL ;
SCHULZ, J ;
GUNTHER, S ;
DUDENHAUSEN, JW ;
BERGMANN, KE ;
BAUER, CP ;
DORSCH, W ;
SCHMIDT, E ;
LUCK, W ;
LAU, S ;
GRASS, T ;
WAHN, U .
ALLERGY, 1995, 50 (01) :65-71
[2]  
Bjerke T, 1994, Pediatr Allergy Immunol, V5, P88, DOI 10.1111/j.1399-3038.1994.tb00223.x
[3]   Umbilical cord blood mononuclear cell proliferative response to house dust mite does not predict the development of allergic rhinitis and asthma [J].
Chan-Yeung, M ;
Ferguson, A ;
Chan, H ;
Dimich-Ward, H ;
Watson, W ;
Manfreda, J ;
Becker, A .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1999, 104 (02) :317-321
[4]   Studies of cord blood mononuclear cell responses and allergy: still in their infancy? [J].
Devereux, G ;
Barker, RN .
CLINICAL AND EXPERIMENTAL ALLERGY, 2002, 32 (03) :331-334
[5]   Influence of atopic heredity on IL-4-, IL-12- and IFN-γ-producing cells in in vitro activated cord blood mononuclear cells [J].
Gabrielsson, S ;
Söderlund, A ;
Nilsson, C ;
Lilja, G ;
Nordlund, M ;
Troye-Blomberg, M .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2001, 126 (03) :390-396
[6]   CORD BLOOD IGE AND MONTH OF BIRTH [J].
KIMPEN, J ;
CALLAERT, H ;
EMBRECHTS, P ;
BOSMANS, E .
ARCHIVES OF DISEASE IN CHILDHOOD, 1987, 62 (05) :478-482
[7]  
Kondo N, 1998, CLIN EXP ALLERGY, V28, P1340
[8]   High interleukin-13 production by phytohaemagglutinin- and Der p 1-stimulated cord blood mononuclear cells is associated with the subsequent development of atopic dermatitis at the age of 3 years [J].
Lange, J ;
Ngoumou, G ;
Berkenheide, S ;
Moseler, M ;
Mattes, J ;
Kuehr, J ;
Kopp, MV .
CLINICAL AND EXPERIMENTAL ALLERGY, 2003, 33 (11) :1537-1543
[9]   The childhood origins of asthma (COAST) study [J].
Lemanske, RF .
PEDIATRIC ALLERGY AND IMMUNOLOGY, 2002, 13 :38-43
[10]  
Liao SY, 1996, CLIN EXP ALLERGY, V26, P397, DOI 10.1046/j.1365-2222.1996.d01-325.x