Jackson A M, Alexandroff A B, McIntyre M, Esuvaranathan K, James K, Chisholm G D
Department of Surgery, University of Edinburgh.
J Clin Pathol. 1994 Apr;47(4):309-12. doi: 10.1136/jcp.47.4.309.
To determine the expression of intercellular adhesion molecule 1 and 2 (ICAM 1 and 2) in transitional cell carcinoma cells before and after immunotherapy with Calmette-Guérin bacillus (BCG).
Frozen sections from 22 untreated bladder carcinomas were immunohistochemically examined with monoclonal antibodies to ICAM 1 and 2. Urinary cytospin slides were made for six patients for each of the six clinical instillations which constitute a therapeutic course. These slides were also stained for ICAM 1 and for leucocyte function associated antigen 1 (LFA 1).
Bladder cancer cells did not essentially express either ICAM 1 or 2, but cells in the stromal areas surrounding tumour expressed both these antigens. After repeated instillations of BCG organisms ICAM 1 positive normal and neoplastic epithelial cells were observed in the urine. Cells obtained from the first three instillations expressed lower densities of ICAM 1 than those from the later instillations. Many neutrophils expressing LFA-1 and some lymphocytes were also noted in the cytospin slides and some of these were conjugated to tumour cells expressing ICAM 1. Six months after treatment a single maintenance dose of BCG induced ICAM 1 expression.
Untreated superficial bladder carcinoma cells do not express ICAM 1 or 2, but these important immunological molecules were expressed in the stromal areas of tissue. Importantly, neoplastic cells in the urine expressed ICAM 1 after immunotherapy. This molecule can render bladder tumour cells vulnerable to non-antigen specific cytotoxicity mediated by activated lymphocytes.
确定卡介苗(BCG)免疫治疗前后移行细胞癌细胞中细胞间黏附分子1和2(ICAM 1和2)的表达情况。
用抗ICAM 1和2的单克隆抗体对22例未经治疗的膀胱癌冰冻切片进行免疫组织化学检查。为6例患者制作尿细胞离心涂片,用于构成一个疗程的6次临床灌注中的每次灌注。这些涂片也进行ICAM 1和白细胞功能相关抗原1(LFA 1)染色。
膀胱癌细胞基本上不表达ICAM 1或2,但肿瘤周围基质区域的细胞表达这两种抗原。反复灌注BCG后,尿液中观察到ICAM 1阳性的正常和肿瘤上皮细胞。前三次灌注获得的细胞ICAM 1表达密度低于后几次灌注获得的细胞。在细胞离心涂片中还观察到许多表达LFA-1的中性粒细胞和一些淋巴细胞,其中一些与表达ICAM 1的肿瘤细胞结合。治疗6个月后,单次维持剂量的BCG诱导ICAM 1表达。
未经治疗的浅表性膀胱癌细胞不表达ICAM 1或2,但这些重要的免疫分子在组织基质区域表达。重要的是,免疫治疗后尿液中的肿瘤细胞表达ICAM 1。该分子可使膀胱肿瘤细胞易受活化淋巴细胞介导的非抗原特异性细胞毒性作用。