Ravn V, Havsteen H, Thorpe S M
Department of Pathology, Herlev University Hospital, Denmark.
Mod Pathol. 1998 Aug;11(8):709-15.
Monoclonal antibody (MoAb) 1D5 with specificity to the estrogen receptor (ER), MoAb 1A6, and a polyclonal antibody (PoAb) (the latter two with specificity to the progesterone receptor [PgR]) were used to stain microwave-pretreated sections of formalin-fixed, paraffin-embedded normal and malignant endometrial tissues (n = 60). The tissues were previously evaluated for ER and PgR by enzyme immunoassay (EIA) (n = 44) and immunohistochemical analysis of frozen tissue (ICAfroz, n = 59). With results of EIA as a reference, the ER-1D5 method yielded a better agreement on receptor status, i.e., positive versus negative (74 vs. 51%) and a higher sensitivity (71 vs. 45%) but a similar high specificity (100%) than the ER-ICA method. Compared with results of PgR-EIA, the immunohistochemical assays for PgR gave similar results as to agreement (86-95%) and sensitivity (95-97%). Quantitative agreement on the fraction of cells stained for ER and PgR by immunohistochemical analysis in frozen and formalin-fixed tissue was obtained in approximately 60% of the cases. The results of semiquantitation were correlated with the results of both ICA and EIA. The MoAbs 1D5 and 1A6, as well as the anti-PgR PoAb, thus seem to be valid for evaluation of ER and PgR status in formalin-fixed endometrial tissue. Differences in the specificity of the Abs and in the sensitivity of the methods used to demonstrate ER and PgR might explain some of the discordant findings.
使用对雌激素受体(ER)具有特异性的单克隆抗体(MoAb)1D5、MoAb 1A6和一种多克隆抗体(PoAb)(后两者对孕激素受体[PgR]具有特异性)对福尔马林固定、石蜡包埋的正常和恶性子宫内膜组织(n = 60)的微波预处理切片进行染色。这些组织先前已通过酶免疫测定(EIA)(n = 44)和冷冻组织的免疫组织化学分析(ICAfroz,n = 59)对ER和PgR进行了评估。以EIA结果为参考,与ER-ICA方法相比,ER-1D5方法在受体状态方面,即阳性与阴性(74%对51%)上具有更好的一致性,敏感性更高(71%对45%),但特异性同样高(100%)。与PgR-EIA结果相比,PgR的免疫组织化学测定在一致性(86 - 95%)和敏感性(95 - 97%)方面给出了相似的结果。在大约60%的病例中,通过免疫组织化学分析在冷冻和福尔马林固定组织中对ER和PgR染色的细胞比例获得了定量一致性。半定量结果与ICA和EIA的结果相关。因此,MoAb 1D5和1A6以及抗PgR PoAb似乎可有效评估福尔马林固定的子宫内膜组织中的ER和PgR状态。抗体特异性以及用于检测ER和PgR的方法敏感性的差异可能解释了一些不一致的发现。