Inoue T, Matsuura E, Nagata A, Ogasawara Y, Hattori A, Kuroki Y, Fujimoto S, Akino T
Immunology Laboratory, Yamasa Corporation, Chiba, Japan.
J Immunol Methods. 1994 Aug 1;173(2):157-64. doi: 10.1016/0022-1759(94)90295-x.
We developed a simple and sensitive enzyme-linked immunosorbent assay (ELISA) for human pulmonary surfactant protein D (SP-D). Human SP-D was purified from bronchoalveolar lavage fluids of patients with pulmonary alveolar proteinosis. Nine monoclonal antibodies (MAbs) were established from BALB/c mice immunized with the purified human SP-D. All MAbs were directed to either 43 kDa SP-D contained in lung lavage fluids of patients with pulmonary alveolar proteinosis or in amniotic fluids from healthy normal pregnancies. The ELISA is based on a sandwich method using two MAbs, 6B2 and 7C6. Cross-reactivity to human SP-A or rat SP-D was evaluated as below 0.6%. The recovery of different concentrations of SP-D ranged from 94.4% to 111.2%, and serial dilutions of amniotic fluids showed good linearity. SP-D concentrations in 21 amniotic fluids from normal pregnancies were measured by the ELISA. The mean concentration in amniotic fluids from pregnancies in the third trimester was significantly higher than that from earlier stages of gestation (p < 0.001), indicating that this ELISA may be applicable for prediction of fetal lung maturity.
我们开发了一种用于检测人肺表面活性物质蛋白D(SP-D)的简单且灵敏的酶联免疫吸附测定法(ELISA)。人SP-D是从肺泡蛋白沉积症患者的支气管肺泡灌洗液中纯化得到的。用纯化的人SP-D免疫BALB/c小鼠,制备了9种单克隆抗体(MAb)。所有单克隆抗体均针对肺泡蛋白沉积症患者肺灌洗液或健康正常妊娠羊水所含的43 kDa SP-D。该ELISA基于使用两种单克隆抗体6B2和7C6的夹心方法。与人SP-A或大鼠SP-D的交叉反应率评估为低于0.6%。不同浓度SP-D的回收率在94.4%至111.2%之间,羊水系列稀释显示出良好的线性关系。用该ELISA检测了21份正常妊娠羊水样本中的SP-D浓度。妊娠晚期羊水的平均浓度显著高于妊娠早期(p<0.001),表明该ELISA可能适用于预测胎儿肺成熟度。