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The immunohistochemical analysis of membrane-bound CD55 CD59 and fluid-phase FH and FH-like complement inhibitors in cancers of ovary and corpus uteri origin

机译:膜结合的CD55CD59和液相FH和FH样补体抑制剂在卵巢和子宫体起源癌中的免疫组织化学分析

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摘要

One of the potential therapeutic methods of cancer treatment is the immunotherapy with monoclonal antibodies. This kind of therapy, although devoid of serious side effects, has often insufficient efficacy. The presence of complement inhibitors on the cancer cells, which are able to inactivate complement-mediated immune response represents one of the main reasons for the inefficiency of such therapy. In our studies we investigated the expression of main membrane–bound and fluid-phase complement regulators: CD55, CD59 and factor H/factor H-like in tumour samples of ovarian and corpus uteri cancer. Tissue samples were collected from 50 patients and stained immunohistochemically, with the use of peroxidase-based immunodetection system. Immunohistochemical analysis revealed that complement inhibitors are present in examined tumors although their presence is heterogenous. The most prevalent is the presence of factor H/H-like, localized mostly in tumor stroma and within vascular structures. Membrane bound complement inhibitors are less prominently expressed by cancer cells. CD55 was detected in low percentage of cells, predominantly within cancer tubules. CD59 immunoreactivity was more prevalent in cancer cells, and was localized particularly at the margin of cancer cell tubules. Our results demonstrate that the most prominent complement inhibitor in cancer of ovary and corpus uteri origin is factor H/factor H-like. Blocking or downregulation of this inhibitor should be taken into consideration with regards to improving the efficiency of immunotherapy with monoclonal antibodies.
机译:癌症治疗的潜在治疗方法之一是单克隆抗体的免疫治疗。这种疗法尽管没有严重的副作用,但通常疗效不足。能够使补体介导的免疫反应失活的癌细胞上补体抑制剂的存在代表了这种疗法无效的主要原因之一。在我们的研究中,我们研究了卵巢癌和子宫癌的肿瘤样本中主要的膜结合和液相补体调节因子CD55,CD59和H因子/ H因子样表达的表达。使用基于过氧化物酶的免疫检测系统从50例患者中收集组织样本并进行免疫组织化学染色。免疫组织化学分析显示补体抑制剂存在于检查的肿瘤中,尽管它们的存在是异质的。最普遍的是H / H样因子的存在,主要位于肿瘤基质和血管结构内。膜结合的补体抑制剂在癌细胞中不太显着表达。 CD55在低百分比的细胞中被检测到,主要在癌症小管内。 CD59免疫反应性在癌细胞中更为普遍,尤其是定位在癌细胞小管的边缘。我们的结果表明,在卵巢和子宫体起源的癌症中最主要的补体抑制剂是H因子/ H因子样。就提高单克隆抗体免疫疗法的效率而言,应考虑该抑制剂的阻断或下调。

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