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膀胱内灌注卡介苗治疗后浅表性膀胱肿瘤患者尿液中白细胞介素2的检测

Detection of interleukin 2 in the urine of patients with superficial bladder tumors after treatment with intravesical BCG.

作者信息

Haaff E O, Catalona W J, Ratliff T L

出版信息

J Urol. 1986 Oct;136(4):970-4. doi: 10.1016/s0022-5347(17)45142-1.

Abstract

Adjuvant intravesical BCG therapy is an effective means of treating superficial bladder tumors. The mechanism by which BCG mediates antitumor activity is not known; however, clinical and animal studies suggest that immunological responsiveness to BCG antigens correlates with antitumor activity. In this report the detection of interleukin 2 (IL-2, a lymphokine produced in response to BCG) in urine specimens of patients treated with intravesical BCG is reported. Patients with superficial transitional cell carcinoma of the bladder received intravesical BCG once each week for six weeks. No intradermal injections were administered. Urine specimens were obtained prior to BCG instillation and four, eight and 24 hours afterwards. The specimens were dialysed, concentrated five-fold and assayed for the presence of IL-2 in a biological assay using an IL-2 dependent cultured T-cell line. IL-2 was detected in urine but not serum after intravesical BCG instillation. IL-2 was characterized by absorption against an IL-2-dependent T cell line and neutralization by monoclonal anti-IL-2 antibodies. No IL-2 was detected in specimens obtained prior to BCG instillation or from donors with no detectable bladder pathology. One of 10 urine specimens from patients with urinary tract infections had detectable IL-2 levels. IL-2 production generally peaked during the fourth to sixth intravesical BCG treatment. Production was short-term in that IL-2 levels peaked four to eight hours after BCG instillation and were rarely (six of 54 specimens) observed 24 hours after instillation. Mean IL-2 levels were higher in patients who were rendered tumor free after BCG therapy but statistical significance was not achieved. Ten of 12 patients (83%) who responded to BCG therapy had urine IL-2 levels greater than or equal to 1.6 units/ml. at least once during the six week treatment period while two of six (33%) patients not responding to therapy had similar urine IL-2 levels. These results show that intravesical BCG therapy induces the production of lymphokines including IL-2. The presence of BCG-induced lymphokines may be associated with anti-tumor activity.

摘要

膀胱内卡介苗辅助治疗是治疗浅表性膀胱肿瘤的一种有效方法。卡介苗介导抗肿瘤活性的机制尚不清楚;然而,临床和动物研究表明,对卡介苗抗原的免疫反应性与抗肿瘤活性相关。本报告报道了在用膀胱内卡介苗治疗的患者尿液标本中白细胞介素2(IL-2,一种对卡介苗产生反应而产生的淋巴因子)的检测情况。患有浅表性膀胱移行细胞癌的患者每周接受一次膀胱内卡介苗治疗,共六周。未进行皮内注射。在卡介苗灌注前以及灌注后4、8和24小时采集尿液标本。将标本进行透析,浓缩5倍,并使用依赖IL-2的培养T细胞系通过生物学测定法检测IL-2的存在。膀胱内卡介苗灌注后在尿液中检测到IL-2,但血清中未检测到。IL-2的特征是可被依赖IL-2的T细胞系吸收,并被单克隆抗IL-2抗体中和。在卡介苗灌注前采集的标本或来自无明显膀胱病变的供体的标本中未检测到IL-2。10份来自尿路感染患者的尿液标本中有1份检测到可检测水平的IL-2。IL-2的产生通常在膀胱内卡介苗治疗的第四至第六次期间达到峰值。产生是短期的,因为IL-2水平在卡介苗灌注后4至8小时达到峰值,而在灌注后24小时很少观察到(54份标本中有6份)。卡介苗治疗后无肿瘤的患者平均IL-2水平较高,但未达到统计学显著性。12名对卡介苗治疗有反应的患者中有10名(83%)在六周治疗期间至少有一次尿液IL-2水平大于或等于1.6单位/毫升,而6名无反应患者中有2名(33%)有类似的尿液IL-2水平。这些结果表明,膀胱内卡介苗治疗可诱导包括IL-2在内的淋巴因子的产生。卡介苗诱导的淋巴因子的存在可能与抗肿瘤活性有关。

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