Tillyer C R, Iqbal J, Raymond J, Gore M, McIlwain T J
Department of Chemical Pathology, Royal Marsden Hospital, Sutton, Surrey.
J Clin Pathol. 1991 Jun;44(6):466-71. doi: 10.1136/jcp.44.6.466.
An immunoturbidimetric assay for the assessment of free kappa and lambda light chains of immunoglobulins was developed using a commercial polyclonal antiserum with reactivity towards epitopes on the light chains, which are not expressed when they are bound to heavy chains. The assay, on a centrifugal analyser, is simple and rapid. The limit of detection is 5 mg/l of free light chain, with an assay range of 5-120 mg/l, intrabatch precisions from 1.5-6.4%, and interbatch precisions from 6.5-8.9%. The assay was only slightly less sensitive than colloidal gold staining of cellulose acetate electrophoreses for the detection of Bence-Jones protein in urine. For the serial monitoring of response to chemotherapy in patients with myeloma, the assay correlated well with serum paraprotein estimates obtained by densitometric scanning of Ponceau stained cellulose acetate electrophoreses, but not with serum beta-2 microglobulin measurements, even after correction for the effects of creatinine. These assays may prove to be of use for the monitoring of tumour response in the treatment of Bence-Jones myeloma.
开发了一种免疫比浊法,用于评估免疫球蛋白的游离κ和λ轻链,该方法使用了一种对轻链表位具有反应性的商业多克隆抗血清,当轻链与重链结合时这些表位不表达。在离心分析仪上进行该检测,操作简单且快速。检测限为5mg/l游离轻链,检测范围为5 - 120mg/l,批内精密度为1.5 - 6.4%,批间精密度为6.5 - 8.9%。该检测方法在检测尿液中本-周蛋白方面,其灵敏度仅略低于醋酸纤维素电泳的胶体金染色法。对于骨髓瘤患者化疗反应的系列监测,该检测与通过对丽春红染色的醋酸纤维素电泳进行光密度扫描获得的血清副蛋白估计值相关性良好,但与血清β-2微球蛋白测量值无关,即使校正了肌酐的影响也是如此。这些检测方法可能被证明可用于监测本-周蛋白骨髓瘤治疗中的肿瘤反应。