首页> 外文期刊>Journal of Translational Medicine >Pre-immature dendritic cells (PIDC) pulsed with HPV16 E6 or E7 peptide are capable of eliciting specific immune response in patients with advanced cervical cancer
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Pre-immature dendritic cells (PIDC) pulsed with HPV16 E6 or E7 peptide are capable of eliciting specific immune response in patients with advanced cervical cancer

机译:用HPV16 E6或E7肽脉冲的未成熟树突状细胞(PIDC)能够引发晚期宫颈癌患者的特异性免疫反应

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Background The protein products of the early genes E6 and E7 in high-risk HPV types 16 and 18 have been implicated in the oncogenic capability of these viruses. Therefore, these peptides represent attractive vaccine therapy targets. Methods Thirty-two patients with advanced cervical cancer (HPV16 or 18 positive) were treated with HPV16 E6 (18–26) (Arm A) or HPV16 E7 (12–20) peptide (Arm B) pulsed on PBMCs in order to illicit immune response against the relevant peptide on both arms. These PBMCs were cultured for a short time (48?hours only) and in the presence of GM- CSF, accordingly, they were identified as “Pre-Immature Dentritic Cells”. Results 51Cr release assay and ELISPOT demonstrated evidence of specific immune response against the relevant peptide in 10/16 (63%) evaluable patients in arm A and 7/12 (58%) in arm B. HPV16 E6 was found to be homologous to HPV18 E6 in both vivo and vitro. The median overall survival (OS) and progression free survival (PFS) for the full cohort was 10.0 and 3.5?months, respectively. There were no RECIST responses in any patient. The majority of toxicities were grade I and II. Conclusions We demonstrated the feasibility and ability of Pre-Immature Dentritic Cells pulsed with HPV16 E6 (18–26) or HPV16 E7 (12–20) to induce a specific immune response against the relevant peptide despite the advanced disease of the cervical cancer patients treated on this trial. We believe that this observation deserves further investigations.
机译:背景高风险HPV 16和18型早期基因E6和E7的蛋白质产物与这些病毒的致癌能力有关。因此,这些肽代表有吸引力的疫苗治疗靶标。方法对32例晚期宫颈癌(HPV16或18阳性)患者行PBMC脉冲HPV16 E6(18–26)(Arm A)或HPV16 E7(12–20)肽(Arm B)治疗,以进行非法免疫对双臂上相关肽的应答。这些PBMC在GM-CSF存在的情况下短时间(仅48小时)培养,因此被鉴定为“未成熟树突状细胞”。结果51Cr释放测定法和ELISPOT证明了在A组的10/16(63%)可评估患者和B组的7/12(58%)的患者中针对相关肽的特异性免疫反应的证据。发现HPV16 E6与HPV18同源E6在体内和体外均可。整个队列的中位总体生存期(OS)和无进展生存期(PFS)分别为10.0和3.5个月。任何患者均无RECIST反应。大部分毒性为I级和II级。结论我们证明了尽管接受了宫颈癌治疗的晚期疾病,但用HPV16 E6(18–26)或HPV16 E7(12–20)脉冲的未成熟树突状细胞诱导针对相关肽的特异性免疫反应的可行性和能力在这个审判中。我们认为这一观察值得进一步研究。

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