Department of Infectious, Parasitic and Immunomediated Diseases, ISS, Rome, Italy.
Vaccine. 2012 Jun 22;30(30):4490-8. doi: 10.1016/j.vaccine.2012.04.069. Epub 2012 May 3.
A novel vaccine (PEV7) consisting of a truncated, recombinant aspartyl proteinase-2 of Candida albicans incorporated into influenza virosomes was studied. This vaccine candidate generated a potent serum antibody response in mouse and rat following intramuscular immunization. Anti-Sap2 IgG and IgA were also detected in the vaginal fluid of rats following intravaginal or intramuscular plus intravaginal administration. In a rat model of candidal vaginitis, PEV7 induced significant, long-lasting, likely antibody-mediated, protection following intravaginal route of immunization. PEV7 was also found to be safe in a repeated-dose toxicological study in rats. Overall, these data provide a sound basis to envisage the clinical development of this new candidate vaccine against candidal vaginitis.
一种新型疫苗(PEV7)由白念珠菌的截短重组天冬氨酸蛋白酶-2和流感病毒囊膜组成。该疫苗候选物在小鼠和大鼠中经肌肉内免疫后产生了强烈的血清抗体反应。在阴道内或肌肉内加阴道内给药后,大鼠阴道分泌物中也检测到抗 Sap2 IgG 和 IgA。在念珠菌性阴道炎大鼠模型中,PEV7 经阴道途径免疫后诱导了显著、持久、可能由抗体介导的保护作用。在大鼠重复剂量毒性研究中,也发现 PEV7 是安全的。总的来说,这些数据为评估这种新型候选疫苗防治念珠菌性阴道炎的临床开发提供了坚实的基础。