Farrow Anitra L, Peng Binghao J, Gu Linlin, Krendelchtchikov Alexandre, Matthews Qiana L
Division of Infectious Diseases, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Division of Pulmonary, Allergy and Critical Medicine, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Viruses. 2016 Mar 10;8(3):78. doi: 10.3390/v8030078.
Due to the increasing amount of people afflicted worldwide with Chagas disease and an increasing prevalence in the United States, there is a greater need to develop a safe and effective vaccine for this neglected disease. Adenovirus serotype 5 (Ad5) is the most common adenovirus vector used for gene therapy and vaccine approaches, but its efficacy is limited by preexisting vector immunity in humans resulting from natural infections. Therefore, we have employed rare serotype adenovirus 48 (Ad48) as an alternative choice for adenovirus/Chagas vaccine therapy. In this study, we modified Ad5 and Ad48 vectors to contain T. cruzi's amastigote surface protein 2 (ASP-2) in the adenoviral early gene. We also modified Ad5 and Ad48 vectors to utilize the "Antigen Capsid-Incorporation" strategy by adding T. cruzi epitopes to protein IX (pIX). Mice that were immunized with the modified vectors were able to elicit T. cruzi-specific humoral and cellular responses. This study indicates that Ad48-modified vectors function comparable to or even premium to Ad5-modified vectors. This study provides novel data demonstrating that Ad48 can be used as a potential adenovirus vaccine vector against Chagas disease.
由于全球感染恰加斯病的人数不断增加,且在美国的发病率也在上升,因此更迫切需要为这种被忽视的疾病开发一种安全有效的疫苗。5型腺病毒(Ad5)是基因治疗和疫苗研发中最常用的腺病毒载体,但其疗效受到人类因自然感染而产生的预先存在的载体免疫的限制。因此,我们采用了罕见血清型腺病毒48(Ad48)作为腺病毒/恰加斯病疫苗治疗的替代选择。在本研究中,我们对Ad5和Ad48载体进行了改造,使其在腺病毒早期基因中包含克氏锥虫无鞭毛体表面蛋白2(ASP-2)。我们还通过在蛋白IX(pIX)上添加克氏锥虫表位,对Ad5和Ad48载体进行改造,以利用“抗原衣壳掺入”策略。用改造后的载体免疫的小鼠能够引发克氏锥虫特异性体液和细胞反应。本研究表明,Ad48改造后的载体功能与Ad5改造后的载体相当,甚至更优。本研究提供了新的数据,证明Ad48可作为一种潜在的抗恰加斯病腺病毒疫苗载体。