Moltó L, Alvarez-Mon M, Carballido J, Olivier C, Gimeno F, Manzano L
Department of Medicine, Hospital Universitario Principe de Asturias, Universidad de Alcalá de Henares, Madrid, Spain.
Cancer. 1995 Jun 1;75(11):2720-6. doi: 10.1002/1097-0142(19950601)75:11<2720::aid-cncr2820751114>3.0.co;2-4.
The evolution of superficial transitional cell carcinoma (TCC) of the bladder poses a clinical management problem due to its tendency to recur after initial transurethral resection (TUR). Natural Killer (NK) cells are a distinct subset of lymphocytes that possess the ability to lyse tumor cells without prior sensitization in a nonmajor histocompatibility-restricted fashion. These cytotoxic cells constitute a relevant barrier against the local growth and systemic dissemination of neoplastic diseases.
The immunomodulatory effect, after TUR of the tumor, of the prophylactic treatment with intravesical instillations of interferon-alpha-2b (IFN-alpha-2b) upon the NK activity of peripheral blood mononuclear cells (PBMNC) in 17 patients with superficial TCC of the bladder was analyzed using a 4-hour 51sodium chromate (51Cr)-release cytotoxicity assay against both NK-sensitive, or K562, and NK-resistant, or JY, tumor target cells.
There were no significant modifications of the NK activity of PBMNC during the 3 months of IFN-alpha-2b intracavitary treatment (P > 0.05). However, with respect to their levels before treatment, NK activity in PBMNC at 3 months posttreatment was enhanced significantly in the 14 patients who showed no sign of tumor recurrence in the 12 months of follow-up (P < 0.01). Six months after finishing the intracavitary IFN-alpha-2b instillations, the PBMNC NK activity in these patients had returned to the levels found before initiating the therapy (P > 0.05). This temporary enhancement of the PBMNC NK activity was not found in three patients with evidence of tumor recurrence at some time during the 12 months after treatment. In similar experimental conditions, significant enhancement of the NK activity in PBMNC was not observed in nine patients with superficial bladder TCC who were treated with intracavitary instillations of mitomycin C (MMC) after the TUR of the tumor and who were free of recurrence of the disease at 1 year of follow up.
The prophylactic intracavitary treatment of superficial bladder TCC with IFN-alpha-2b may induce an immunomodulatory effect in the NK activity of PBMNC that appears to be associated with the clinical evolution of the disease.
膀胱浅表性移行细胞癌(TCC)的演变带来了临床管理难题,因为其在初次经尿道切除术(TUR)后有复发倾向。自然杀伤(NK)细胞是淋巴细胞的一个独特亚群,具有以非主要组织相容性限制方式在无需预先致敏的情况下裂解肿瘤细胞的能力。这些细胞毒性细胞构成了对抗肿瘤疾病局部生长和全身扩散的一道相关屏障。
采用针对NK敏感的K562和NK耐药的JY肿瘤靶细胞的4小时51铬酸钠(51Cr)释放细胞毒性试验,分析17例膀胱浅表性TCC患者在肿瘤TUR后经膀胱内灌注干扰素-α-2b(IFN-α-2b)进行预防性治疗对外周血单个核细胞(PBMNC)NK活性的免疫调节作用。
在IFN-α-2b腔内治疗的3个月期间,PBMNC的NK活性无显著改变(P>0.05)。然而,与治疗前水平相比,在随访12个月未出现肿瘤复发迹象的14例患者中,治疗后3个月时PBMNC中的NK活性显著增强(P<0.01)。完成腔内IFN-α-2b灌注6个月后,这些患者的PBMNC NK活性已恢复至开始治疗前的水平(P>0.05)。在治疗后12个月内某些时间有肿瘤复发证据的3例患者中未发现PBMNC NK活性的这种暂时增强。在类似的实验条件下,9例膀胱浅表性TCC患者在肿瘤TUR后经膀胱内灌注丝裂霉素C(MMC)治疗且随访1年无疾病复发,未观察到PBMNC中NK活性的显著增强。
用IFN-α-2b对膀胱浅表性TCC进行预防性腔内治疗可能会在PBMNC的NK活性中诱导一种免疫调节作用,这似乎与疾病的临床演变相关。