FC-GAMMA RECEPTOR IIA (CD32) POLYMORPHISM IN FULMINANT MENINGOCOCCAL SEPTIC SHOCK IN CHILDREN

被引:157
作者
BREDIUS, RGM
DERKX, BHF
FIJEN, CAP
DEWIT, TPM
DEHAAS, M
WEENING, RS
VANDEWINKEL, JGJ
OUT, TA
机构
[1] ACAD MED CTR,DEPT PEDIAT,CLIN IMMUNOL LAB,1100 DE AMSTERDAM,NETHERLANDS
[2] EMMA CHILDRENS HOSP,CLIN & LAB IMMUNOL UNIT,AMSTERDAM,NETHERLANDS
[3] UNIV AMSTERDAM,CLIN & EXPTL IMMUNOL LAB,AMSTERDAM,NETHERLANDS
[4] UNIV AMSTERDAM,DEPT MED MICROBIOL,REFERENCE LAB BACTERIAL MENINGITIS,AMSTERDAM,NETHERLANDS
[5] NATL INST PUBL HLTH & ENVIRONM PROTECT,AMSTERDAM,NETHERLANDS
[6] UNIV UTRECHT HOSP,DEPT IMMUNOL,UTRECHT,NETHERLANDS
关键词
D O I
10.1093/infdis/170.4.848
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Antibodies are essential in host defense against Neisseria meningitidis. Therefore, interactions among IgG and Fc receptors (Fc gamma R) on phagocytes may be crucial. Genetic polymorphic forms of Fc gamma RIIa (CD32) express different functional activities. In a retrospective study, Fc gamma R polymorphisms were determined in 25 children who survived fulminant meningococcal septic shock: 11 had Fc gamma RIIa-R/R131, the poor IgG2-binding allotype, which is a significantly more frequent rate than found in a healthy white population (44% vs. 23%; P = .028; odds ratio = 2.67; 95% confidence interval, 1.09-6.53). The relevance of this finding was further supported by the fact that neutrophils with the Fc gamma RIIa-R/R131 allotype phagocytized N. meningitidis opsonized with polyclonal IgG2 antibodies less effectively than did IIa-H/H131 neutrophils. Our findings suggest an important role for anti-N. meningitidis IgG2 and the Fc gamma RIIa polymorphism in host defense against systemic meningococcal infections.
引用
收藏
页码:848 / 853
页数:6
相关论文
共 37 条
[1]  
ABO T, 1984, J EXP MED, V160, P303
[2]   A COMPARISON OF THE VARIABLE ANTIGENS EXPRESSED BY CLONE-IV-1 AND SUBGROUP-III OF NEISSERIA-MENINGITIDIS SEROGROUP-A [J].
ACHTMAN, M ;
KUSECEK, B ;
MORELLI, G ;
EICKMANN, K ;
WANG, JF ;
CROWE, B ;
WALL, RA ;
HASSANKING, M ;
MOORE, PS ;
ZOLLINGER, W .
JOURNAL OF INFECTIOUS DISEASES, 1992, 165 (01) :53-68
[3]   COMPLEMENT ACTIVATION BY POLYCLONAL IMMUNOGLOBULIN-G1 AND IMMUNOGLOBULIN-G2 ANTIBODIES AGAINST STAPHYLOCOCCUS-AUREUS, HAEMOPHILUS-INFLUENZAE TYPE-B, AND TETANUS TOXOID [J].
BREDIUS, RGM ;
DRIEDIJK, PC ;
SCHOUTEN, MFJ ;
WEENING, RS ;
OUT, TA .
INFECTION AND IMMUNITY, 1992, 60 (11) :4838-4847
[4]  
BREDIUS RGM, 1993, J IMMUNOL, V151, P1463
[5]   GENETIC-LINKAGE OF HEREDITARY MOTOR AND SENSORY NEUROPATHY TYPE-I (CHARCOT-MARIE-TOOTH DISEASE) TO MARKERS OF CHROMOSOME-1 AND CHROMOSOME-17 [J].
DEFESCHE, JC ;
HOOGENDIJK, JE ;
DEVISSER, M ;
DEVISSER, BWO ;
BOLHUIS, PA .
NEUROLOGY, 1990, 40 (09) :1450-1453
[6]   POLYMORPHISM OF IGG FC-RECEPTORS IN MENINGOCOCCAL DISEASE [J].
FIJEN, CAP ;
BREDIUS, RGM ;
KUIJPER, EJ .
ANNALS OF INTERNAL MEDICINE, 1993, 119 (07) :636-636
[7]  
FIJEN CAP, 1989, LANCET, V2, P585
[8]   FREQUENCY OF THE POLYMORPHONUCLEAR NEUTROPHIL FC-GAMMA RECEPTOR-III DEFICIENCY IN THE FRENCH POPULATION AND ITS INVOLVEMENT IN THE DEVELOPMENT OF NEONATAL ALLOIMMUNE NEUTROPENIA [J].
FROMONT, P ;
BETTAIEB, A ;
SKOURI, H ;
FLOCH, C ;
POULET, E ;
DUEDARI, N ;
BIERLING, P .
BLOOD, 1992, 79 (08) :2131-2134
[9]   HUMAN IMMUNITY TO MENINGOCOCCUS .I. ROLE OF HUMORAL ANTIBODIES [J].
GOLDSCHNEIDER, I ;
GOTSCHLICH, EC ;
ARTENSTEIN, MS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1969, 129 (06) :1307-+
[10]  
GOSSELIN EJ, 1990, J IMMUNOL, V144, P1817