Immunohistochemical features of HLA-DR antigen expression and lymphoid infiltrates in gastric carcinoma after low-dose interleukin-2 and mitomycin C.

H Inoue, S Arinaga, M Adachi, T Asoh, H Ueo, T Akiyoshi
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Abstract

We immunohistochemically evaluated lymphoid cell infiltration and HLA-DR antigen expression in gastric tumor tissue obtained from advanced gastric cancer patients 1 day after the completion of the treatment with mitomycin C (MMC) 12 mg/m2 i.v. on day 1 and recombinant interleukin-2 (IL-2) i.v. every 12 h from day 4 through day 8. Then the results were compared with those in 11 patients pretreated with MMC alone, 5 treated with IL-2 alone, and 24 untreated patients. Widespread lymphoid infiltration was observed in 17% of untreated tumors, 27% of MMC-pretreated tumors, and 40% of tumors treated with IL-2 alone. However, 71% of carcinomas pretreated with MMC plus IL-2 exhibited widespread infiltration. The frequency of cases with high-grade infiltration of CD4+ cells was significantly higher in either group of patients treated with MMC alone or MMC plus IL-2. Because the CD8+ cell infiltration was not significantly altered, the ratio of CD4+ to CD8+ cells estimated as being > 1 was more frequently noted in patients given MMC alone or MMC plus IL-2, as compared with untreated control. Furthermore, 86% of tumors pretreated with MMC plus IL-2 exhibited positive HLA-DR antigen expression, whereas 29% of untreated carcinomas did so. MMC or IL-2 alone did not significantly increase HLA-DR expression. These results indicate that the combination of low-dose of IL-2 with MMC enhances the intensity of lymphoid cell infiltration in tumors, with the predominance of CD4+ cells, and HLA-DR antigen expression on tumor cells in patients with advanced gastric carcinoma.

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低剂量白细胞介素-2和丝裂霉素C对胃癌中HLA-DR抗原表达和淋巴浸润的免疫组织化学特征
我们用免疫组织化学方法评估晚期胃癌患者治疗结束后1天的胃肿瘤组织淋巴细胞浸润和HLA-DR抗原表达,第1天静脉注射丝分裂霉素C (MMC) 12mg /m2,第4天至第8天每12 h静脉注射重组白细胞介素-2 (IL-2)。然后将结果与单独接受MMC治疗的11例患者、单独接受IL-2治疗的5例患者和未接受治疗的24例患者进行比较。17%未治疗的肿瘤、27% mmc预处理的肿瘤和40%单独使用IL-2治疗的肿瘤存在广泛的淋巴浸润。然而,71%的MMC + IL-2预处理的癌表现出广泛的浸润。在单独使用MMC或MMC加IL-2治疗的两组患者中,CD4+细胞高级别浸润的病例频率均显着增加。由于CD8+细胞浸润没有明显改变,与未治疗的对照组相比,单独使用MMC或MMC加IL-2的患者中CD4+ / CD8+细胞的比值估计大于1的情况更常见。此外,86%经MMC + IL-2预处理的肿瘤表现出HLA-DR抗原阳性表达,而未经治疗的肿瘤则为29%。单独使用MMC或IL-2均未显著增加HLA-DR的表达。上述结果提示,低剂量IL-2联合MMC可增强晚期胃癌患者肿瘤淋巴样细胞浸润强度,以CD4+细胞为主,并可增强肿瘤细胞HLA-DR抗原表达。
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