[肿瘤内注射生物反应调节剂(BRM)对荷瘤宿主的免疫调节作用]。

Nihon Gan Chiryo Gakkai shi Pub Date : 1990-08-20
K Okuno, I Nakajima, Y Shilayama, T Hirohata, H Ohnishi, Y Nakamura, T Nakamura, M Yasutomi
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引用次数: 0

摘要

胃癌患者术前内镜下瘤内注射生物反应调节剂(BRM),如由减毒链球菌组成的化合物OK432,已被尝试,与单纯手术切除相比,该方法改善了预后。我们试图通过实验小鼠系统来阐明这一机制,并在这里证明了OK432的术前IT可以显著延长生存时间并诱导脾脏中肿瘤特异性细胞毒性T淋巴细胞(CTL)。相比之下,肿瘤坏死因子(TNF) IT虽然能显著减小原发肿瘤的大小,但不能延长生存期,也不能诱导特异性CTL反应。为了分析OK432 IT诱导全身CTL反应的原因,我们从OK432注射的肿瘤块中收集活的肿瘤细胞和浸润的盘贴细胞,用流式细胞仪检测I类和II类抗原的表达。肿瘤细胞I类和II类抗原表达不变,但经OK432预处理后,II类阳性贴壁细胞明显增加。与上述结果相同,在胃癌标本中,组织学发现OK432预处理后的朗格汉斯细胞显著增加,该细胞具有强大的抗原呈递功能,且II类抗原呈阳性。综上所述,这些发现强烈表明,OK432 IT通过级联反应增强了II类阳性抗原呈递细胞(APC)的活性,最终导致了体内抗肿瘤效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Immunomodulating effect of intratumoral (IT) injection of biological response modifiers (BRM) on tumor-bearing hosts].

Preoperative endoscopic intratumoral injection (IT) of biological response modifiers (BRM), such as OK432, a compound composed of attenuated Streptococcus pyogens, in gastric cancer patients has been tried and this method has been improving the prognosis compared to surgical resection only. We tried to clarify this mechanism using experimental mouse system and demonstrated here the preoperative IT of OK432 significantly prolonged the survival and induced the tumor-specific cytotoxic T lymphocytes (CTL) in the spleen. By contrast, tumor necrosis factor (TNF) IT failed to prolong the survival and to induce specific CTL response, although it reduced primary tumor size significantly. To analyze why OK432 IT induce the systemic CTL response, viable tumor cells and infiltrating dish-adherent cells from the OK432 injected tumor mass were harvested and examined the class I and class II antigen expression by flow cytometer. Class I and class II antigen expression of the tumor cells remained unchanged, however, the class II positive dish-adherent cells markedly increased by OK432 pretreatment. As same in these results, histological finding in gastric cancer specimen has shown prominent increase of Langerhans cells, possessing potent antigen-presenting function and positive class II antigen, by OK432 pretreatment. Taken together, these findings strongly suggest that the increased class II positive antigen-presenting cells (APC) activity by OK432 IT augment the CTL response via cascade reaction and finally, resulted in anti-tumor efficacy in vivo.

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