Najam F I, Giasuddin A S, Shembesh A H
Department of Laboratory Medicine (Clinical Immunological Unit), Faculty of Medicine, Al-Arab Medical University, Benghazi, Libya.
Indian J Pediatr. 1999 May-Jun;66(3):337-44. doi: 10.1007/BF02845519.
Immunoglobulin isotypes (IgG, IgA, IgM, IgD, IgE) in serum were investigated in 64 Libyan children with mild to moderately severe asthma (age: 1-12 years; sex: 39 males, 25 females) (Group A) and in 57 healthy Libyan children (age: 1-12 years; sex: 30 males, 27 females (Group B). The patients were classified according to age into three groups (A1: 1-3 years; A2: > 3-5 years; A3: > 5-12 years); according to disease activity into two groups (AA: active disease; NA: inactive disease); and according to age plus disease activity into six groups (AA1, NA1; AA2, NA2; AA3, NA3). The healthy children were also divided according to age into three groups (B1: 1-3 years; B2: > 3-5 years; B3: > 5-12 years). IgG, IgA, IgM and IgD were measured by radial immunodiffusion method and IgE was estimated by enzyme immunoassay technique utilizing immunokits from bioMerieux, France. Serum levels of IgG, IgD and IgE were elevated significantly in patients compared to controls (A vs B: p < 0.05) while IgA and IgM levels were normal (p > 0.05). IgG and IgD levels were raised in A3 (p < 0.05), while IgD levels were raised in both A2 and A3 (p < 0.05) and IgE was elevated in all age groups (p < 0.05). However, IgG was elevated significantly in AA only, while IgD and IgE levels were high in both AA and NA (p < 0.05) and IgE was even considerably higher in AA compared to NA (p < 0.02). Further elevated levels were observed for IgG in AA3 only (p < 0.05), for IgD in NA2 (p < 0.01), AA3 (p < 0.01) and NA3 (p < 0.05) and IgE was much higher in patients with active disease than with inactive disease in all age groups (p < 0.05). The fact that asthmatic attack in majority of our patients can be explained as mediated through IgE and the possibilities that IgG and IgD may play roles as aetiopathogenetic or protective regulatory factors in childhood asthma are discussed.
对64名患有轻度至中度严重哮喘的利比亚儿童(年龄:1至12岁;性别:男39名,女25名)(A组)和57名健康的利比亚儿童(年龄:1至12岁;性别:男30名,女27名)(B组)的血清免疫球蛋白同种型(IgG、IgA、IgM、IgD、IgE)进行了研究。患者按年龄分为三组(A1:1至3岁;A2:大于3至5岁;A3:大于5至12岁);按疾病活动度分为两组(AA:活动期疾病;NA:非活动期疾病);按年龄加疾病活动度分为六组(AA1、NA1;AA2、NA2;AA3、NA3)。健康儿童也按年龄分为三组(B1:1至3岁;B2:大于3至5岁;B3:大于5至12岁)。采用放射免疫扩散法测定IgG、IgA、IgM和IgD,采用酶免疫测定技术,利用法国生物梅里埃公司的免疫试剂盒测定IgE。与对照组相比,患者的血清IgG、IgD和IgE水平显著升高(A组与B组比较:p<0.05),而IgA和IgM水平正常(p>0.05)。A3组的IgG和IgD水平升高(p<0.05),A2组和A3组的IgD水平均升高(p<0.05),所有年龄组的IgE水平均升高(p<0.05)。然而,仅AA组的IgG显著升高,而AA组和NA组的IgD和IgE水平均较高(p<0.05),且AA组的IgE水平比NA组更高(p<0.02)。仅AA3组的IgG水平进一步升高(p<0.05),NA2组(p<0.01)、AA3组(p<0.01)和NA3组(p<0.05)的IgD水平升高,所有年龄组中活动期疾病患者的IgE水平比非活动期疾病患者高得多(p<0.05)。讨论了我们大多数患者的哮喘发作可解释为通过IgE介导这一事实,以及IgG和IgD可能作为儿童哮喘的病因发病或保护性调节因子发挥作用的可能性。