CHU Lille, Institut d'Immunologie, Lille, France.
CHU Lille, Institut d'Immunologie, Centre de Biologie-Pathologie-Génétique, F-59000 Lille, France.
Clin Chem Lab Med. 2018 Jul 26;56(8):1319-1327. doi: 10.1515/cclm-2018-0001.
Immunoglobulin G (IgG) and IgG subclass assays are indicated in patients with suspected primary immunodeficiency (PID). Commercially available assays for IgG subclass determination are calibrated against various preparations, and so specific reference values are required for each of them. Using Optilite® reagents from The Binding Site Group Ltd., we sought to determine the pediatric IgG and IgG subclass reference intervals with respect to the ERM-DA470k certified reference material.
Levels of IgG and IgG subclasses were analyzed in serum samples collected from a large cohort of PID-free children and adolescents. Reference intervals were calculated for previously published age groups (6-12 months, 12-18 months, 18 months-2 years, 2-3 years, 3-4 years, 4-6 years, 6-9 years, 9-12 years and 12-18 years), according to the Clinical and Laboratory Standards Institute's C28-A3c protocol.
A total of 456 serum samples were analyzed. The correlation between the total IgG and the sum of the IgG subclasses was good (r2=0.96). No statistically significant gender-specific differences were observed. Our results for the changes over time in IgG and IgG subclass levels are consistent with previous reports. The differences between our lower/upper reference limits and those in the literature are probably due to variations in calibration.
Our present results provide a reliable basis for the diagnosis of PIDs in childhood and for the accreditation of laboratories using Optilite® immunoturbidimetric reagents for IgG subclass measurement. Laboratory scientists and clinicians should be aware of the need for manufacturer-specific IgG subclass reference intervals.
免疫球蛋白 G(IgG)和 IgG 亚类测定用于疑似原发性免疫缺陷(PID)患者。市售的 IgG 亚类测定试剂盒针对不同的制剂进行校准,因此每种试剂盒都需要特定的参考值。我们使用来自 The Binding Site Group Ltd. 的 Optilite®试剂,旨在根据 ERM-DA470k 认证参考物质确定儿科 IgG 和 IgG 亚类参考区间。
从大量无 PID 的儿童和青少年的血清样本中分析 IgG 和 IgG 亚类的水平。根据临床和实验室标准协会的 C28-A3c 方案,根据先前发表的年龄组(6-12 个月、12-18 个月、18 个月-2 岁、2-3 岁、3-4 岁、4-6 岁、6-9 岁、9-12 岁和 12-18 岁)计算参考区间。
共分析了 456 个血清样本。总 IgG 与 IgG 亚类总和之间的相关性良好(r2=0.96)。未观察到性别特异性差异。我们关于 IgG 和 IgG 亚类水平随时间变化的结果与之前的报告一致。我们的参考下限和上限与文献中的差异可能归因于校准的差异。
我们目前的结果为儿童 PID 的诊断以及使用 Optilite®免疫比浊法试剂进行 IgG 亚类测量的实验室认证提供了可靠的依据。实验室科学家和临床医生应该意识到需要特定制造商的 IgG 亚类参考区间。