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抗表皮生长因子抗体对表皮生长因子/表皮生长因子受体结合的有效抑制,与接受表皮生长因子癌症疫苗治疗的晚期非小细胞肺癌患者更好的生存率相关。

Effective inhibition of the epidermal growth factor/epidermal growth factor receptor binding by anti-epidermal growth factor antibodies is related to better survival in advanced non-small-cell lung cancer patients treated with the epidermal growth factor cancer vaccine.

作者信息

García Beatriz, Neninger Elia, de la Torre Ana, Leonard Idrissa, Martínez Rocío, Viada Carmen, González Gisela, Mazorra Zaima, Lage Agustín, Crombet Tania

机构信息

Center of Molecular Immunology, Clinical Imunology Department, Havana, Cuba.

出版信息

Clin Cancer Res. 2008 Feb 1;14(3):840-6. doi: 10.1158/1078-0432.CCR-07-1050.

Abstract

PURPOSE

Epidermal growth factor (EGF) might be a suitable immunotherapeutic target in non-small-cell lung cancer (NSCLC). Our approach consists of active immunotherapy with EGF. The aim of the study is to characterize the humoral response and its effects on signal transduction in relation with the clinical outcome.

EXPERIMENTAL DESIGN

Eighty NSCLC patients treated with first-line chemotherapy were randomized to receive the EGF vaccine or supportive care. EGF concentration in sera, anti-EGF antibodies and their capacity to inhibit the binding between EGF/EGF receptor (EGFR), and the EGFR phosphorylation were measured.

RESULTS

Seventy-three percent of vaccinated patients developed a good antibody response, whereas none of the controls did. In good antibody-responder patients, self EGF in sera was significantly reduced. In 58% of vaccinated patients, the post-immune sera inhibited EGF/EGFR binding; in the control group, no inhibition occurred. Post-immune sera inhibited the EGFR phosphorylation whereas sera from control patients did not have this capacity. Good antibody-responder patients younger than 60 years had a significantly better survival. A high correlation between anti-EGF antibody titers, EGFR phosphorylation inhibition, and EGF/EGFR binding inhibition was found. There was a significantly better survival for vaccinated patients that showed the higher capacity to inhibit EGF/EGFR binding and for those who showed an immunodominance by the central region of EGF molecule.

CONCLUSIONS

Immunization with the EGF vaccine induced neutralizing anti-EGF antibodies capable of inhibiting EGFR phosphorylation. There was a significant positive correlation between antibody titers, EGF/EGFR binding inhibition, immunodominance of anti-EGF antibodies, and survival in advanced NSCLC patients.

摘要

目的

表皮生长因子(EGF)可能是非小细胞肺癌(NSCLC)中一个合适的免疫治疗靶点。我们的方法包括用EGF进行主动免疫治疗。本研究的目的是表征体液反应及其对信号转导的影响,并将其与临床结果相关联。

实验设计

80例接受一线化疗的NSCLC患者被随机分为接受EGF疫苗或支持治疗。测量血清中的EGF浓度、抗EGF抗体及其抑制EGF/表皮生长因子受体(EGFR)之间结合的能力,以及EGFR磷酸化水平。

结果

73%接种疫苗的患者产生了良好的抗体反应,而对照组无一产生。在抗体反应良好的患者中,血清中的自身EGF显著降低。58%接种疫苗的患者,免疫后的血清抑制了EGF/EGFR结合;在对照组中,未出现抑制现象。免疫后的血清抑制了EGFR磷酸化,而对照患者的血清没有这种能力。60岁以下抗体反应良好的患者生存期明显更长。发现抗EGF抗体滴度、EGFR磷酸化抑制和EGF/EGFR结合抑制之间存在高度相关性。对于显示出较高抑制EGF/EGFR结合能力的接种疫苗患者以及那些在EGF分子中心区域表现出免疫优势的患者,其生存期明显更好。

结论

用EGF疫苗免疫诱导了能够抑制EGFR磷酸化的中和性抗EGF抗体。在晚期NSCLC患者中,抗体滴度、EGF/EGFR结合抑制、抗EGF抗体的免疫优势与生存期之间存在显著正相关。

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