Hallez Sophie, Simon Philippe, Maudoux Frédéric, Doyen Jean, Noël Jean-Christophe, Beliard Aude, Capelle Xavier, Buxant Frédéric, Fayt Isabelle, Lagrost Anne-Cécile, Hubert Pascale, Gerday Colette, Burny Arsène, Boniver Jacques, Foidart Jean-Michel, Delvenne Philippe, Jacobs Nathalie
Chimie Biologique, Institut de Biologie et de Médecine Moléculaires, Université Libre de Bruxelles, 12 rue des Professeurs Jeener et Brachet, 6041 Gosselies, Belgium.
Cancer Immunol Immunother. 2004 Jul;53(7):642-50. doi: 10.1007/s00262-004-0501-4. Epub 2004 Feb 17.
Infection with oncogenic human papillomavirus (HPV) and HPV-16 in particular is a leading cause of anogenital neoplasia. High-grade intraepithelial lesions require treatment because of their potential to progress to invasive cancer. Numerous preclinical studies have demonstrated the therapeutic potential of E7-directed vaccination strategies in mice tumour models. In the present study, we tested the immunogenicity of a fusion protein (PD-E7) comprising a mutated HPV-16 E7 linked to the first 108 amino acids of Haemophilus influenzae protein D, formulated in the GlaxoSmithKline Biologicals adjuvant AS02B, in patients bearing oncogenic HPV-positive cervical intraepithelial neoplasia (CIN).
Seven patients, five with a CIN3 and two with a CIN1, received three intramuscular injections of adjuvanted PD-E7 at 2-week intervals. Three additional CIN1 patients received a placebo. CIN3 patients underwent conization 8 weeks postvaccination. Cytokine flow cytometry and ELISA were used to monitor antigen-specific cellular and antibody responses from blood taken before and after vaccine or placebo injection.
Some patients had preexisting systemic IFN-gamma CD4+ (1/10) and CD8+ (5/10) responses to PD-E7. Vaccination, not placebo injection, elicited systemic specific immune responses in the majority of the patients. Five vaccinated patients (71%) showed significantly increased IFN-gamma CD8+ cell responses upon PD-E7 stimulation. Two responding patients generated long-term T-cell immunity toward the vaccine antigen and E7 as well as a weak H. influenzae protein D (PD)-directed CD4+ response. All the vaccinated patients, but not the placebo, made significant E7- and PD-specific IgG.
The encouraging results obtained from this study performed on a limited number of subjects justify further analysis of the efficacy of the PD-E7/AS02B vaccine in CIN patients.
致癌性人乳头瘤病毒(HPV)感染,尤其是HPV-16感染,是肛门生殖器肿瘤形成的主要原因。高级别上皮内病变因其有进展为浸润性癌的可能而需要治疗。众多临床前研究已在小鼠肿瘤模型中证实了E7导向疫苗接种策略的治疗潜力。在本研究中,我们测试了一种融合蛋白(PD-E7)的免疫原性,该融合蛋白由与流感嗜血杆菌蛋白D的前108个氨基酸相连的突变型HPV-16 E7组成,用葛兰素史克生物制品公司的佐剂AS02B配制,用于患有致癌性HPV阳性宫颈上皮内瘤变(CIN)的患者。
7例患者,5例为CIN3,2例为CIN1,每隔2周接受3次肌肉注射佐剂PD-E7。另外3例CIN1患者接受安慰剂。CIN3患者在接种疫苗8周后进行锥切术。采用细胞因子流式细胞术和酶联免疫吸附测定法监测疫苗或安慰剂注射前后采集的血液中抗原特异性细胞和抗体反应。
部分患者先前存在对PD-E刺激的全身性γ干扰素CD4+(1/10)和CD8+(5/10)反应。接种疫苗而非注射安慰剂在大多数患者中引发了全身性特异性免疫反应。5例接种疫苗的患者(71%)在PD-E刺激后显示γ干扰素CD8+细胞反应显著增加。2例有反应的患者对疫苗抗原和E产生了长期T细胞免疫,以及对流感嗜血杆菌蛋白D(PD)的弱导向CD4+反应。所有接种疫苗的患者而非安慰剂组产生了显著的E7和PD特异性IgG。
在有限数量的受试者中进行的本研究获得的令人鼓舞的结果,证明有必要进一步分析PD-E7/AS02B疫苗在CIN患者中的疗效。