Lymphocyte subset populations in children with polysaccharide antibody deficiency following cardiac transplantation

被引:5
作者
Gennery, AR
Barge, D
Spickett, GP
Cant, AJ
机构
[1] Newcastle Gen Hosp, Dept Paediat Immunol, Newcastle Upon Tyne NE4 6BE, Tyne & Wear, England
[2] Royal Victoria Infirm, Dept Immunol, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
关键词
polysaccharide antibodies; antibody deficiency; immunosuppression; cardiac transplantation; B-cell maturation; CD21receptor;
D O I
10.1023/A:1006741015452
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Pneumococcal polysaccharide (PPS) antibody deficiency occurs in some children immunosuppressed following cardiac transplantation in early childhood. We studied lymphocyte subset populations in these children to identify patterns associated with antibody deficiency, particularly in CD21 + B cells. Lymphocyte surface markers CD3, CD4, CD8, CD19, and CD21 were measured on whole blood by FACS analysis in four patient groups: cardiac transplant patients who did and did not respond to PPS, nontransplanted cardiac patients, and normal controls. Absolute cell numbers were compared with agerelated normal ranges. The proportion of children with values below the age-related 25th percentile in each group was compared. Normal controls had significantly more CD3 +, CD8 +, and CD19+ cells, even when age-related differences were accounted for. Control groups had significantly more CD19 cells than transplant patients and transplanted PPS responders and cardiac controls had more mature B cells (CD21+) than transplanted PPS nonresponders. PPS antibody deficiency following pediatric cardiac transplantation may be related to an immaturity in B cells due to immunosuppression commenced in early childhood.
引用
收藏
页码:37 / 42
页数:6
相关论文
共 22 条
[1]  
ABDOU NI, 1973, CLIN EXP IMMUNOL, V13, P55
[2]   IGG AND IGM PNEUMOCOCCAL POLYSACCHARIDE ANTIBODY-RESPONSES IN INFANTS [J].
BARRETT, DJ ;
LEE, CG ;
AMMANN, AJ ;
AYOUB, EM .
PEDIATRIC RESEARCH, 1984, 18 (11) :1067-1071
[3]  
BATIUK TD, 1994, TRANSPLANT P, V26, P2831
[4]  
BERNER V, 1996, EUR J IMMUNOL, V26, P1481
[5]  
BREARLEY S, 1987, CLIN EXP IMMUNOL, V70, P322
[6]  
COOPER NR, 1988, ANNU REV IMMUNOL, V6, P85
[7]   Role of the NF-ATc transcription factor in morphogenesis of cardiac valves and septum [J].
de la Pompa, JL ;
Timmerman, LA ;
Takimoto, H ;
Yoshida, H ;
Elia, AJ ;
Samper, E ;
Potter, J ;
Wakeham, A ;
Marengere, L ;
Langille, BL ;
Crabtree, GR ;
Mak, TW .
NATURE, 1998, 392 (6672) :182-186
[8]  
DIMITRIU A, 1978, J IMMUNOL, V121, P2335
[9]   EFFECTS OF CYCLOSPORIN-A ON THE IMMUNE-SYSTEM OF THE MOUSE .1. EVIDENCE FOR A DIRECT SELECTIVE EFFECT OF CYCLOSPORIN-A ON B-CELLS RESPONDING TO ANTI-IMMUNOGLOBULIN ANTIBODIES [J].
DONGWORTH, DW ;
KLAUS, GGB .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1982, 12 (12) :1018-1022
[10]   ANTIBODY-RESPONSE TO PNEUMOCOCCAL VACCINATION IN CHILDREN YOUNGER THAN 5-YEARS OF AGE [J].
DOUGLAS, RM ;
PATON, JC ;
DUNCAN, SJ ;
HANSMAN, DJ .
JOURNAL OF INFECTIOUS DISEASES, 1983, 148 (01) :131-137