Dattatreyamurty B, Sheth A R, Purandare T V, Rao S S
Endocrinology. 1976 Dec;99(6):1554-61. doi: 10.1210/endo-99-6-1554.
Immunological cross-reaction between hCG and anti-oLH sera has been demonstrated using radioimmunoassay techniques. The results indicate that this cross-reaction is incomplete and that the anti-oLH sera used have the ability to distinguish between LH and hCG. Following absorption with purified hCG, anti-oLH serum was used to develop a heterologous radioimmunoassay "[125I]iodo-hLH + anti-oLH serum" (H-O, RIA) which specifically and selectively measures hLH in serum samples containing both hLH and hCG. In this radioimmunoassay hCG and subunits of hCG do not cross-react with hLH, in the range in which these hormones are present in human serum under physiological conditions. Other hormones such as hPL, hPRL, hGH, hFSH, hTSH, and GnRH do not interfere with the measurement of LH by radioimmunoassay. The sensitivity of the assay was 1.5 mIU (25 ng) per ml (LER 907 standard), and the inter- and intra-assay coefficients of variations for samples were 10.83% and 8.4%, respectively. The recoveries of hLH added to pregnancy serum containing an hCG concentration of 8.55 IU/ml were in the range 95-108%. Determination of LH content of human pituitary extracts by H-O RIA gave values which were in close agreement with those derived by bioassay (indices of discrimination 0.72-1.12). Serum LH patterns in women during normal menstrual cycles as well as in amenorrheic patients who received GnRH treatment are comparable to those reported by other investigators using other radioimmunoassay systems. Serum samples obtained during the first trimester of pregnancy, when analyzed by H-O RIA, showed basal LH levels.
利用放射免疫分析技术已证实了人绒毛膜促性腺激素(hCG)与抗促黄体生成素(oLH)血清之间的免疫交叉反应。结果表明,这种交叉反应是不完全的,所使用的抗oLH血清有能力区分促黄体生成素(LH)和人绒毛膜促性腺激素(hCG)。用纯化的hCG吸收后,抗oLH血清被用于开发一种异源放射免疫分析方法“[125I]碘-hLH + 抗oLH血清”(H-O,RIA),该方法能特异性且选择性地检测含有hLH和hCG的血清样本中的hLH。在这种放射免疫分析中,在生理条件下人血清中这些激素存在的范围内,hCG及其亚基不会与hLH发生交叉反应。其他激素,如人胎盘催乳素(hPL)、人催乳素(hPRL)、人生长激素(hGH)、人促卵泡生成素(hFSH)、人促甲状腺激素(hTSH)和促性腺激素释放激素(GnRH),不会干扰放射免疫分析对LH的测定。该分析方法的灵敏度为每毫升1.5毫国际单位(25纳克)(LER 907标准品),样本的批间和批内变异系数分别为10.83%和8.4%。添加到hCG浓度为8.55国际单位/毫升的妊娠血清中的hLH回收率在95%至108%之间。用H-O RIA测定人垂体提取物中的LH含量,所得值与生物测定法得出的值非常一致(鉴别指数为0.72至1.12)。正常月经周期女性以及接受GnRH治疗的闭经患者的血清LH模式与其他使用其他放射免疫分析系统的研究者所报告的结果相当。妊娠头三个月采集的血清样本,经H-O RIA分析显示基础LH水平。