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Regression of Human Papillomavirus Intraepithelial Lesions Is Induced by MVA E2 Therapeutic Vaccine

机译:MVA E2治疗疫苗诱导人乳头瘤病毒上皮内病变的消退

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Human papilloma viruses can induce warts, condylomas, and other intraepithelial cervical lesions that can progress to cancer. Cervical cancer is a serious problem in developing countries because early detection is difficult, and thus proper early treatment is many times missing. In this phase III clinical trial, we evaluated the potential use of MVA E2 recombinant vaccinia virus to treat intraepithelial lesions associated with papillomavirus infection. A total of 1176 female and 180 male patients with intraepithelial lesions were studied. They were injected with 10 7 MVA E2 virus particles directly into their uterus, urethra, vulva, or anus. Patients were monitored by colposcopy and cytology. Immune response was determined by measuring the antibody titer against MVA E2 virus and by analyzing the cytotoxic activity against cancer cells bearing papillomavirus DNA. Papillomavirus was determined by the Hybrid Capture method or by polymerase chain reaction analysis. By histology, 1051 (89.3%) female patients showed complete elimination of lesions after treatment with MVA E2. In 28 (2.4%) female patients, the lesion was reduced to CIN 1. Another 97 (8.3%) female patients presented isolated koilocytes after treatment. In men, all lesions were completely eliminated. All MVA E2-treated patients developed antibodies against the MVA E2 vaccine and generated a specific cytotoxic response against papilloma-transformed cells. Papillomavirus DNA was not detected after treatment in 83% of total patients treated. MVA E2 did not generate any apparent side effects. These data suggest that therapeutic vaccination with MVA E2 vaccine is an excellent candidate to stimulate the immune system and generate regression in intraepithelial lesions when applied locally.
机译:人乳头瘤病毒可诱发疣,con突和其他上皮内宫颈病变,并可能发展为癌症。在发展中国家,子宫颈癌是一个严重的问题,因为很难及早发现,因此很多时候缺乏适当的早期治疗。在此III期临床试验中,我们评估了MVA E2重组痘苗病毒在治疗与乳头瘤病毒感染相关的上皮内病变中的潜在用途。共研究了1176名女性和180名男性上皮内病变患者。他们直接向子宫,尿道,外阴或肛门注射10 7 MVA E2病毒颗粒。通过阴道镜和细胞学监测患者。通过测量针对MVA E2病毒的抗体滴度并通过分析对带有乳头瘤病毒DNA的癌细胞的细胞毒活性来确定免疫应答。乳头瘤病毒通过杂交捕获法或聚合酶链反应分析确定。从组织学上看,用MVA E2治疗后,有1 051名女性患者(89.3%)完全消除了病变。在28名(2.4%)女性患者中,病变减少至CIN1。另外97名(8.3%)女性患者在治疗后出现了分离的空泡细胞。在男性中,所有病变均被完全消除。所有接受MVA E2治疗的患者均产生了针对MVA E2疫苗的抗体,并产生了针对乳头瘤转化细胞的特异性细胞毒性反应。治疗后83%的患者中未检测到乳头瘤病毒DNA。 MVA E2没有产生任何明显的副作用。这些数据表明,当局部应用时,MVA E2疫苗的治疗性疫苗是刺激免疫系统并在上皮内病变中引起消退的极佳候选者。

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