Thorpe R, Wadhwa M, Gearing A, Mahon B, Poole S
National Institute for Biological Standards and Control, Bar, Herts, UK.
Lymphokine Res. 1988 Summer;7(2):119-27.
In order to estimate human IL-1 alpha in physiological samples we have established sensitive and specific immunoradiometric assays using monoclonal and polyclonal antibodies. Solid phase assays employing two different monoclonal antibodies were suitable for estimating rDNA derived IL-1 alpha but were relatively insensitive. Sensitivity was increased by using a monoclonal antibody to capture antigen and 125I-labelled polyclonal sheep antibodies to develop the assay. This assay could detect as little as 20pg/ml IL-1 alpha and could be used for assaying antigen in monocyte supernatants, in human skin extracts and in joint fluid from patients with inflammatory disease. It was entirely specific for IL-1 alpha and was unaffected by non-IL-1 alpha components present in serum. It is therefore suitable for monitoring IL-1 alpha concentrations in the circulation of patients undergoing therapy with the monokine.
为了在生理样本中检测人白细胞介素-1α(IL-1α),我们利用单克隆抗体和多克隆抗体建立了灵敏且特异的免疫放射分析方法。采用两种不同单克隆抗体的固相分析方法适用于检测重组DNA衍生的IL-1α,但相对不够灵敏。通过使用单克隆抗体捕获抗原,并用125I标记的多克隆羊抗体进行检测,提高了检测灵敏度。该分析方法能够检测低至20pg/ml的IL-1α,可用于检测单核细胞上清液、人皮肤提取物以及炎症性疾病患者关节液中的抗原。它对IL-1α具有完全特异性,不受血清中存在的非IL-1α成分的影响。因此,它适用于监测接受该单核因子治疗患者循环中的IL-1α浓度。