Yamaguchi Y, Miyahara E, Ohshita A, Kawabuchi Y, Ohta K, Shimizu K, Minami K, Hihara J, Sawamura A, Toge T
Department of Surgical Oncology, Research Institute for Radiation Biology and Medicine, Hiroshima University, Japan.
Br J Cancer. 2003 Nov 17;89(10):1876-84. doi: 10.1038/sj.bjc.6601379.
In total, 16 patients with cytologically proven malignant effusion from colorectal cancer were treated by locoregional administration of the streptococcal preparation OK-432 alone or OK-432 plus the T-cell growth factor interleukin (IL)-2, and the action mechanism of the treatment was studied. A positive clinical response, showing a cytologic disappearance of cancer cells and decrease of effusion, was observed in nine of 11 (82%) patients treated with OK-432 alone and in all five patients treated with OK-432 plus IL-2. Flow cytometric analysis revealed that OK-432 plus IL-2 locally induced acute inflammation-like responses, including serial cellular infiltrations of granulocyte migration within a matter of hours, and activation of macrophages and T lymphocyte involvement within the following days, and that a predominant expansion of CD3+CD4+ lymphocytes (CD: cluster of differentiation) was induced by in vitro stimulation with IL-2 of locoregional cells after the OK-432 administration (OK/IL-2AK cells). The OK/IL-2AK cells produced tumour necrosis factor-alpha and interferon-gamma, but these cells did not produce IL-4 and IL-6. The OK/IL-2AK cells expressed potent killing activity against autologous tumour cells. This activity was abrogated by treatment of the lymphocytes with anti-CD3, -CD4, -TCRalphabeta antibody, and by the treatment of target cells with anti-human leukocyte antigen (HLA)-DR antibody. The OK/IL-2AK cells expressed Fas-L gene, and flow cytometric analysis demonstrated HLA-DR expression in approximately 75% of CEA+ or cytokeratin+ effusion cells. TCRVbeta gene analysis of the OK/IL-2AK cells showed an oligoclonal usage of TCRbeta20, which was also involved in the cytotoxic mechanism of the OK/IL-2AK cells. Single-strand conformational polymorphism analysis demonstrated the clonotypes for the TCRVbeta20 gene, and the CDR3s of the gene were sequenced. The clonotypic PCR using the TCRVbeta20-CDR3 sequences could detect the CDR3-identical TCRs in effusion lymphocytes from the other patients. Taken together, it is suggested that locoregional administration of OK-432 plus IL-2 is highly effective for the management of malignant effusion from colorectal cancer. OK-432 plus IL-2 induces autologous tumour-reactive CD4+ Th1 killer lymphocytes, which recognise tumour antigen(s) presented with HLA class II molecules on effusion tumour cells by means of preferential usage of TCRVbeta20. The clonotypic PCR using the TCRVbeta20-CDR3 sequences may be informative for treating malignant effusion from colorectal cancer using OK-432 plus IL-2.
总共16例经细胞学证实为结直肠癌恶性积液的患者接受了局部注射链球菌制剂OK-432单独治疗或OK-432联合T细胞生长因子白细胞介素(IL)-2治疗,并对该治疗的作用机制进行了研究。在单独接受OK-432治疗的11例患者中有9例(82%)以及接受OK-432联合IL-2治疗的所有5例患者中均观察到了阳性临床反应,表现为癌细胞的细胞学消失和积液减少。流式细胞术分析显示,OK-432联合IL-2可在局部诱导急性炎症样反应,包括数小时内粒细胞迁移的一系列细胞浸润,以及随后几天巨噬细胞的激活和T淋巴细胞的参与,并且在给予OK-432后(OK/IL-2AK细胞),局部细胞经IL-2体外刺激可诱导CD3+CD4+淋巴细胞(CD:分化簇)显著扩增。OK/IL-2AK细胞产生肿瘤坏死因子-α和干扰素-γ,但这些细胞不产生IL-4和IL-6。OK/IL-2AK细胞对自体肿瘤细胞表现出强大的杀伤活性。用抗CD3、-CD4、-TCRαβ抗体处理淋巴细胞以及用抗人白细胞抗原(HLA)-DR抗体处理靶细胞可消除这种活性。OK/IL-2AK细胞表达Fas-L基因,流式细胞术分析显示约75%的CEA+或细胞角蛋白+积液细胞表达HLA-DR。对OK/IL-2AK细胞的TCRVβ基因分析显示TCRβ20呈寡克隆使用,这也参与了OK/IL-2AK细胞的细胞毒性机制。单链构象多态性分析显示了TCRVβ20基因的克隆型,并对该基因的CDR3进行了测序。使用TCRVβ20-CDR3序列的克隆型PCR可检测其他患者积液淋巴细胞中CDR3相同的TCR。综上所述,提示局部给予OK-432联合IL-2对结直肠癌恶性积液的治疗非常有效。OK-...联合IL-2诱导自体肿瘤反应性CD4+ Th1杀伤淋巴细胞,这些淋巴细胞通过优先使用TCRVβ20识别积液肿瘤细胞上与HLA II类分子呈递的肿瘤抗原。使用TCRVβ20-CDR3序列的克隆型PCR可能有助于使用OK-432联合IL-2治疗结直肠癌恶性积液。