James-Ellison M Y, Roberts R, Verrier-Jones K, Williams J D, Topley N
Department of Child Health University of Wales College of Medicine, Cardiff Royal Infirmary, UK.
Clin Nephrol. 1997 Aug;48(2):69-78.
The incidence of primary urinary tract infection (UTI) is greatest in the first month of life and decreases with age throughout childhood. Secretory immunoglobulin A (sIgA) is an important component of mucosal immunity. The changes in secretory IgA, IgA and free secretory component (FSC) during the first year of life were examined in relation to age, sex and in infants, feeding practice. These constituents were further compared between healthy children and those with acute and recurrent UTI. Urine was collected from 41 healthy infants (16 female: 25 male) at intervals (mean age 1.4, 9.1, 44, 91, 210 and 412 days), 139 healthy children (75 female: 64 male), 29 children with histories of recurrent UTI (25 female: 4 male) and 10 with acute UTI (8 female: 2 male). sIgA, IgA and FSC were measured by enzyme linked immunoassay. In the majority of children sIgA and IgA were undetectable at birth. SIgA and IgA rose significantly during the first year then levelled off throughout childhood. FSC was detectable from birth (geometric mean [mean of logged values]-GOM at day 1.4, 362.2 ng/ml). No sex differences were apparent for any of the three constituents at any age. Breast feeding was associated with higher levels of sIgA and IgA than bottle feeding. This was highly significant at 9.1 days when sIgA and IgA levels of breast fed compared with bottle fed infants were 64.6 ng/ml vs 21.2 and 56.2 ng/ml vs 18.7 ng/ml respectively, giving a GOM ratio of 3.04 for sIgA and 3.0 for IgA (p < 0.001 for both). No significant difference in the three parameters were demonstrable when children with recurrent UTI-with normal or abnormal renal tracts-were compared with controls. Acute UTI resulted in raised sIgA, IgA and FSC compared with controls (GOM ratio of 4.9 [p < 0.002], 4.2 [p < 0.005] and 2.7 [p < 0.001] respectively). The proportion of total IgA present as sIgA (sIgA/total IgA) was not significantly different in the acute vs control groups. Urinary sIgA and IgA may be important for the observed variation with age in infant UTI and the reduced incidence in breast fed infants but does not appear to contribute to the sex associated difference in susceptibility to infection at any age.
原发性尿路感染(UTI)的发病率在出生后的第一个月最高,在整个儿童期随年龄增长而降低。分泌型免疫球蛋白A(sIgA)是黏膜免疫的重要组成部分。研究了生命第一年中分泌型IgA、IgA和游离分泌成分(FSC)随年龄、性别以及婴儿喂养方式的变化。还对健康儿童与急性和复发性UTI患儿的这些成分进行了进一步比较。从41名健康婴儿(16名女性:25名男性)在不同时间点(平均年龄1.4、9.1、44、91、210和412天)、139名健康儿童(75名女性:64名男性)、29名有复发性UTI病史的儿童(25名女性:4名男性)和10名急性UTI患儿(8名女性:2名男性)收集尿液。通过酶联免疫吸附测定法测量sIgA、IgA和FSC。在大多数儿童中,出生时无法检测到sIgA和IgA。sIgA和IgA在出生后的第一年显著上升,然后在整个儿童期趋于平稳。FSC从出生时就可检测到(第1.4天的几何平均值[对数值的平均值]-GOM为362.2 ng/ml)。在任何年龄,这三种成分中的任何一种都没有明显的性别差异。母乳喂养的婴儿sIgA和IgA水平高于奶瓶喂养的婴儿。在9.1天时差异极为显著,母乳喂养婴儿与奶瓶喂养婴儿的sIgA水平分别为64.6 ng/ml对21.2 ng/ml,IgA水平分别为56.2 ng/ml对18.7 ng/ml,sIgA的GOM比值为3.04,IgA为3.0(两者p均<0.001)。将有复发性UTI(肾道正常或异常)的儿童与对照组进行比较时,这三个参数没有显著差异。与对照组相比,急性UTI导致sIgA、IgA和FSC升高(GOM比值分别为4.9 [p<0.002]、4.2 [p<0.005]和2.7 [p<0.001])。急性组与对照组中以sIgA形式存在的总IgA比例(sIgA/总IgA)没有显著差异。尿液中的sIgA和IgA可能对婴儿UTI中观察到的年龄差异以及母乳喂养婴儿发病率降低很重要,但似乎对任何年龄感染易感性的性别相关差异没有影响。