van der Meijden A P, Steerenberg P A, van Hoogstraaten I M, Kerckhaert J A, Schreinemachers L M, Harthoorn-Lasthuizen E J, Hagenaars A M, de Jong W H, Debruijne F M, Ruitenberg E J
Department of Urology, Radboud University Hospital, Nijmegen.
Cancer Immunol Immunother. 1989;28(4):287-95. doi: 10.1007/BF00205239.
The immune reactivity of patients with strongly recurrent superficial bladder cancer was followed after combined intravesical and intradermal bacillus Calmette-Guérin (BCG) immunotherapy. All patients in this study were previously treated without success with intravesical chemotherapy. The BCG treatment regimen consisted of weekly administrations with BCG (RIVM) for six consecutive weeks, both intravesically and intradermally. In this study, sera and peripheral blood leukocytes (PBL) of patients were tested serially. Besides BCG-antigen-specific reactions, e.g. skin reactivity to purified protein derivatives of Mycobacterium tuberculosis (PPD), antibody formation and antigen stimulation of PBL in vitro, non-antigen-specific immune reactivities were also measured, e.g. mitogen response and spontaneous cytotoxic activity of PBL. In addition the antibody response to bladder carcinoma antigens and the cytotoxic activity of PBL for the bladder carcinoma cell line T24 and the natural-killer-sensitive K562 cell line were investigated. The results obtained from the various assays were evaluated for their prognostic value in relation to the length of the tumor-free interval after the BCG treatment. Because sera and PBL were only obtained during the first 6 months after the BCG treatment, the immune reactivity was compared to the clinical results at that same time. At 6 months after therapy 12 out of 40 BCG-treated patients were tumor-free whereas 28 out of 40 showed a recurrence. Skin reactivity to tuberculin PPD was measured in 40 patients during a period of 3-6 months after therapy. Of patients who showed a recurrence of the tumor within 6 months, 48% of them showed a transient response or developed no response at all to PPD. In the group of patients with a longer tumor-free period (n = 10), only one patient lost the response to tuberculin PPD. Although PBL of a limited number of patients were tested, it was observed that the cytotoxicity to the bladder carcinoma cell line T24, and the natural-killer-sensitive K562 cell line increased in a number of the patients (7 out of 14, and 9 out of 14 respectively). Reactivity of PBL to mitogens and subset distribution (ratio T-helper: T-suppressor/cytotoxic) were not influenced by the BCG treatment. Antibody response to mycobacterial antigen was detected in 9 out of 23 patients investigated. Of these 9 patients, 8 belonged to the group with a recurrence of the tumor within 6 months (n = 17). There was no correlation between the skin reactivity and the antibody response to tuberculin PPD.(ABSTRACT TRUNCATED AT 400 WORDS)
对复发性浅表性膀胱癌患者进行膀胱内和皮内联合卡介苗(BCG)免疫治疗后,对其免疫反应性进行了跟踪研究。本研究中的所有患者此前膀胱内化疗均未成功。BCG治疗方案包括连续六周每周一次膀胱内和皮内注射BCG(荷兰国家公共卫生与环境研究所株)。在本研究中,对患者的血清和外周血白细胞(PBL)进行了连续检测。除了BCG抗原特异性反应,如对结核分枝杆菌纯化蛋白衍生物(PPD)的皮肤反应性、抗体形成以及体外PBL的抗原刺激外,还测量了非抗原特异性免疫反应性,如PBL的丝裂原反应和自发细胞毒性活性。此外,还研究了对膀胱癌抗原的抗体反应以及PBL对膀胱癌细胞系T24和自然杀伤敏感细胞系K562的细胞毒性活性。对各种检测结果进行评估,以确定其与BCG治疗后无瘤间期长度的预后价值。由于血清和PBL仅在BCG治疗后的前6个月获取,因此同时将免疫反应性与临床结果进行了比较。治疗6个月后,40例接受BCG治疗的患者中有12例无肿瘤,而40例中有28例出现复发。在治疗后3 - 6个月期间,对40例患者测量了对结核菌素PPD的皮肤反应性。在6个月内出现肿瘤复发的患者中,48%的患者对PPD表现出短暂反应或根本无反应。在无瘤期较长的患者组(n = 10)中,只有1例患者对结核菌素PPD失去反应。尽管仅对有限数量的患者的PBL进行了检测,但观察到一些患者(分别为14例中的7例和14例中的9例)对膀胱癌细胞系T24和自然杀伤敏感细胞系K562的细胞毒性增加。PBL对丝裂原的反应性和亚群分布(辅助性T细胞:抑制性/细胞毒性T细胞比例)不受BCG治疗的影响。在23例接受调查的患者中,9例检测到对分枝杆菌抗原的抗体反应。在这9例患者中,8例属于6个月内肿瘤复发的组(n = 17)。皮肤反应性与对结核菌素PPD的抗体反应之间无相关性。(摘要截断于400字)