Sanner T, Kotlar H K, Eker P
Cancer Lett. 1980 Feb;8(4):283-90. doi: 10.1016/0304-3835(80)90143-3.
A modified leukocyte adherence inhibition (H-LAI) assay was used to study immunological factors in serum from lung cancer patients. In this test, 0.25% serum was added to the assay system, together with tumor antigen and trypsinized leukocytes from control persons. Extracts from a human lung cancer cell line (Calu-1) and a human breast cancer cell line (MCF-7) were used as antigens. The results obtained were compared with data found with the original hemocytometer (C-LAI) assay. Of 21 lung cancer patients studied, 20 (95%) gave a positive response in both the H-LAI and the C-LAI assay systems against Calu-1 antigen. Only 1 of the patients gave a positive response in the H-LAI system against MCF-7 antigen, while 3 patients (14%) responded in the C-LAI assay. None of the 14 control persons tested gave a positive response. While the C-LAI assay was limited to the use of fresh blood, the H-LAI system was performed on small amounts of serum. The serum could be stored in the frozen state for a long time period. The results indicate that the H-LAI assay possesses at least the same sensitivity and specificity as the original C-LAI test.
采用改良白细胞黏附抑制试验(H-LAI)研究肺癌患者血清中的免疫因子。在该试验中,将0.25%的血清加入检测系统,同时加入肿瘤抗原和来自对照人员经胰蛋白酶处理的白细胞。用人肺癌细胞系(Calu-1)和人乳腺癌细胞系(MCF-7)的提取物作为抗原。将获得的结果与原始血细胞计数器(C-LAI)试验的数据进行比较。在研究的21例肺癌患者中,20例(95%)在H-LAI和C-LAI检测系统中对Calu-1抗原均呈阳性反应。只有1例患者在H-LAI系统中对MCF-7抗原呈阳性反应,而在C-LAI试验中有3例患者(14%)呈阳性反应。14例对照人员检测均无阳性反应。C-LAI试验仅限于使用新鲜血液,而H-LAI系统则用少量血清进行检测。血清可长期冷冻保存。结果表明,H-LAI试验至少与原始C-LAI试验具有相同的敏感性和特异性。