Kadhim S A, Chin J L, Batislam E, Karlik S J, Garcia B, Skamene E
Department of Surgery, London Health Sciences Centre, Ontario, Canada.
J Urol. 1997 Aug;158(2):646-52.
Genetically regulated host response to intravesical Bacillus Calmette Guerin (BCG) immunotherapy was assessed using the murine bladder tumor MM45T in Bcgr and Bcgs inbred congenic strains of mice.
Tumor detection and monitoring of treatment response to BCG was carried out using magnetic resonance imaging (MRI) of BALB/c (Bcgs allele) and BALB/c. CD2 (CD2) (Bcgr allele) mice implanted orthotopically with MM45T tumor cells. Intravesical BCG instillation (3 doses per week for 3 weeks) was used as prophylaxis against tumor implantation in both Bcgr and Bcgs strains and as definitive treatment against MRI-confirmed established tumors. Tumors implanted in both strains of untreated mice served as controls. Intravesical injection of BCG was also performed in established heterotopic subcutaneous tumors in both strains. Immunologic response in all groups was assessed by flow cytometric analysis of the bladder irrigation fluid cell composition, measuring CD4+ (helper/inducer) and CD8+ (cytotoxic/ suppressor) cell subsets.
Intralesional injection of BCG into established heterotopic tumors showed growth inhibition in the Bcgs strain but not in the Bcgr strain. Intravesical BCG treatment against established orthotopic tumors showed significant tumor regression in the Bcgs strain compared to control but there was no effect in the Bcgr strain.
The differential anti-tumor activity of BCG in the Bcgs and Bcgr congenic murine strains supports the notion that Bcg gene-controlled responsiveness to BCG innoculation determines, at least partially, the host response to immunotherapy. These results have potential clinical significance in patient selection for intravesical therapy for bladder cancer.
利用Bcgr和Bcgs近交同源系小鼠的鼠膀胱肿瘤MM45T,评估基因调控的宿主对膀胱内卡介苗(BCG)免疫疗法的反应。
使用原位植入MM45T肿瘤细胞的BALB/c(Bcgs等位基因)和BALB/c.CD2(CD2)(Bcgr等位基因)小鼠,通过磁共振成像(MRI)进行肿瘤检测和对BCG治疗反应的监测。膀胱内灌注BCG(每周3次,共3周)用于预防Bcgr和Bcgs品系中的肿瘤植入,并作为对MRI确诊的已建立肿瘤的确定性治疗。未治疗小鼠的两个品系中植入的肿瘤用作对照。还对两个品系中已建立的异位皮下肿瘤进行了膀胱内注射BCG。通过对膀胱冲洗液细胞组成进行流式细胞术分析,测量CD4 +(辅助/诱导)和CD8 +(细胞毒性/抑制)细胞亚群,评估所有组的免疫反应。
向已建立的异位肿瘤内注射BCG显示在Bcgs品系中肿瘤生长受到抑制,而在Bcgr品系中则没有。与对照相比,针对已建立的原位肿瘤的膀胱内BCG治疗在Bcgs品系中显示出显著的肿瘤消退,但在Bcgr品系中没有效果。
BCG在Bcgs和Bcgr同源小鼠品系中的抗肿瘤活性差异支持了这样一种观点,即Bcg基因控制的对BCG接种的反应性至少部分决定了宿主对免疫疗法的反应。这些结果在膀胱癌膀胱内治疗的患者选择中具有潜在的临床意义。