De Boer L C, Steerenberg P A, Van der Meijden P M, Van Klingeren B, De Jong W H, Elgersma A, Debruyne F M, Ruitenberg E J
Laboratory for Pathology, Dutch National Institute of Public Health and Environmental Protection, (RIVM), Bilthoven, The Netherlands.
J Urol. 1992 Nov;148(5):1577-82. doi: 10.1016/s0022-5347(17)36973-2.
At present, isoniazid (INH) is being used prophylactically to reduce the side effects of intravesical BCG therapy for superficial bladder cancer, although it is not clear whether or not this reduces the antitumor efficacy of BCG. In this study the impact of INH treatment on the immune response after repeated intravesical BCG administration was investigated in guinea pigs. INH was given on the 3 days around each BCG instillation. We found that the administration of INH severely impaired the immunological effects of BCG. The induction of mononuclear cell infiltration in the bladder wall was reduced. Enlargement of the regional lymph nodes (weight and number of cells), and increase of MHC Class II expression on the lymph node cells, normally observed after intravesical BCG administration, were inhibited by INH. Systemic immunity, measured by the DTH reaction in the skin to PPD, was also diminished due to the combined treatment of BCG with INH. When INH was administered during the last 4 of 6 BCG instillations, the immune response to BCG was still impaired. A five-fold increase of the dose of BCG did not overcome the effect of INH. INH probably did not exert a direct suppression of the immune system of the guinea pig as the DNCB skin reactivity was not influenced. Although INH concentrations in the urine were high at the onset of the instillation, in vitro experiments indicated that the effect of INH may not be caused by killing of the BCG organisms shortly after application in the bladder. In conclusion, our data in guinea pigs suggest that the use of INH may impair the immune response to intravesical BCG. As this response may be important for the antitumor effect of BCG, urologists should be cautious with the prophylactic use of INH. The influence on the antitumor efficacy is now investigated in man.
目前,异烟肼(INH)正被用于预防性降低浅表性膀胱癌膀胱内卡介苗(BCG)治疗的副作用,尽管尚不清楚这是否会降低BCG的抗肿瘤疗效。在本研究中,我们在豚鼠身上研究了INH治疗对重复膀胱内给予BCG后免疫反应的影响。在每次BCG灌注前后3天给予INH。我们发现,给予INH会严重损害BCG的免疫效果。膀胱壁单核细胞浸润的诱导减少。通常在膀胱内给予BCG后观察到的局部淋巴结肿大(重量和细胞数量)以及淋巴结细胞上MHC II类表达的增加受到INH的抑制。通过皮肤对PPD的迟发型超敏反应(DTH)测量的全身免疫,也因BCG与INH的联合治疗而减弱。当在6次BCG灌注中的最后4次期间给予INH时,对BCG的免疫反应仍然受损。BCG剂量增加五倍也无法克服INH的作用。由于二硝基氯苯(DNCB)皮肤反应性未受影响,INH可能并未直接抑制豚鼠的免疫系统。尽管在灌注开始时尿液中的INH浓度很高,但体外实验表明,INH的作用可能不是由于在膀胱内应用后不久杀死BCG菌株所致。总之,我们在豚鼠身上的数据表明,使用INH可能会损害对膀胱内BCG的免疫反应。由于这种反应可能对BCG的抗肿瘤作用很重要,泌尿外科医生在预防性使用INH时应谨慎。目前正在人体中研究其对抗肿瘤疗效的影响。