首页> 外文期刊>Molecular cancer therapeutics >Level of HER-2eu protein expression in breast cancer may affect the development of endogenous HER-2eu-specific immunity.
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Level of HER-2eu protein expression in breast cancer may affect the development of endogenous HER-2eu-specific immunity.

机译:乳腺癌中HER-2 / neu蛋白的表达水平可能会影响内源性HER-2 / neu特异性免疫的发展。

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We questioned whether the incidence or magnitude of the humoral or cellular immune response to the self-tumor antigen HER-2eu is influenced by the level of HER-2eu protein overexpression as defined by immunohistochemical staining of tumors in breast cancer patients. We obtained peripheral blood from 104 women with stage II, III, and IV pathologically confirmed HER-2eu-overexpressing breast cancer. Patients were categorized with +1 (n = 14), +2 (n = 20), or +3 (n 70) HER-2eu overexpression by institutional pathologic report. Circulating antibodies to HER-2eu were evaluated using ELISA. T-cell responses to HER-2eu were measured using an antigen-specific tritiated thymidine incorporation assay. Eighty-two percent of subjects with HER-2eu antibodies were +3 overexpressors compared with 18% +2 overexpressors and 0% +1 overexpressors, a highly significant difference (P < 0.001), and there were significant differences in the magnitude of the HER-2eu-specific antibodies between groups with varying HER-2eu protein expression (P = 0.022). In addition, 65% of subjects with HER-2eu-specific T cells were +3 overexpressors compared with 16% +2 overexpressors and 19% +1 overexpressors (P = 0.001). Data presented here indicate that endogenous HER-2eu-specific humoral and T-cell immunity is greater in patients with +3 protein overexpression in their tumors than in patients with lower levels of HER-2eu expression. Overexpression of a self-tumor-associated protein is a potential mechanism by which immunogenicity is enhanced and may aid in the identification of biologically relevant proteins to target for immune-based molecular cancer therapies.
机译:我们质疑乳腺癌患者中对自身肿瘤抗原HER-2 / neu的体液或细胞免疫反应的发生率或强度是否受HER-2 / neu蛋白过表达水平的影响,该水平由肿瘤的免疫组织化学染色确定。我们从104位经II,III和IV期病理证实为HER-2 / neu过表达的乳腺癌女性中获得了外周血。根据机构病理报告,将患者分类为+1(n = 14),+ 2(n = 20)或+3(n 70)HER-2 / neu过表达。使用ELISA评估了针对HER-2 / neu的循环抗体。使用抗原特异性tri化胸苷掺入测定法测量对HER-2 / neu的T细胞应答。拥有HER-2 / neu抗体的受试者中有82%是+3过表达者,而18%+2过表达者和0%+1过表达者,差异有极显着性(P <0.001),并且具有不同HER-2 / neu蛋白表达的组之间的HER-2 / neu特异性抗体(P = 0.022)。此外,有HER-2 / neu特异性T细胞的受试者中有65%是+3过表达者,而16%+2过表达者和19%+1过表达者(P = 0.001)。此处提供的数据表明,肿瘤中+3蛋白过表达的患者的内源性HER-2 / neu特异性体液和T细胞免疫力比HER-2 / neu表达较低的患者更高。自肿瘤相关蛋白的过表达是增强免疫原性的潜在机制,并可能有助于鉴定生物学相关蛋白以靶向基于免疫的分子癌症治疗。

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