Parrino Janie, McCurdy Lewis H, Larkin Brenda D, Gordon Ingelise J, Rucker Steven E, Enama Mary E, Koup Richard A, Roederer Mario, Bailer Robert T, Moodie Zoe, Gu Lin, Yan Lihan, Graham Barney S
Vaccine Research Center, National Institutes of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Vaccine. 2007 Feb 9;25(8):1513-25. doi: 10.1016/j.vaccine.2006.10.047. Epub 2006 Nov 7.
Modified vaccinia Ankara (MVA) was evaluated as an alternative to Dryvax in vaccinia-naïve and vaccinia-immune adult volunteers. Subjects received intramuscular MVA or placebo followed by Dryvax challenge at 3 months. Two or more doses of MVA prior to Dryvax reduced severity of lesion formation, decreased magnitude and duration of viral shedding, and augmented post-Dryvax vaccinia-specific CD8(+) T cell responses and extracellular enveloped virus protein-specific antibody responses. MVA vaccination is safe and immunogenic and improves the safety and immunogenicity of subsequent Dryvax vaccination supporting the potential for using MVA as a vaccine in the general population to improve immunity to orthopoxviruses.
在未接种过牛痘和已接种过牛痘的成年志愿者中,对改良安卡拉痘苗(MVA)作为Dryvax的替代疫苗进行了评估。受试者接受肌肉注射MVA或安慰剂,3个月后接受Dryvax攻击。在接受Dryvax之前接种两剂或更多剂MVA可降低损伤形成的严重程度,减少病毒脱落的幅度和持续时间,并增强Dryvax接种后牛痘特异性CD8(+) T细胞反应和细胞外包膜病毒蛋白特异性抗体反应。MVA疫苗接种安全且具有免疫原性,可提高后续Dryvax疫苗接种的安全性和免疫原性,这支持了将MVA用作普通人群疫苗以提高对正痘病毒免疫力的潜力。