Department of Epidemiology and Public Health, University of Maryland School of Medicine, Baltimore, Maryland 21201, USA.
J Infect Dis. 2010 Dec 1;202(11):1649-58. doi: 10.1086/657087. Epub 2010 Oct 27.
Noroviruses cause significant morbidity and mortality from acute gastroenteritis in all age groups worldwide.
We conducted 2 phase 1 double-blind, controlled studies of a virus-like particle (VLP) vaccine derived from norovirus GI.1 genotype adjuvanted with monophosphoryl lipid A (MPL) and the mucoadherent chitosan. Healthy subjects 18-49 years of age were randomized to 2 doses of intranasal Norwalk VLP vaccine or controls 21 days apart. Study 1 evaluated 5-, 15-, and 50-μg dosages of Norwalk antigen, and study 2 evaluated 50- and 100-μg dosages. Volunteers recorded symptoms for 7 days after dosing, and safety was followed up for 180 days. Blood samples were collected for serological profile, antibody secreting cells (ASCs), and analysis of ASC homing receptors.
The most common symptoms were nasal stuffiness, discharge, and sneezing. No vaccine-related serious adverse events occurred. Norwalk VLP-specific immunoglobulin G and immunoglobulin A antibodies increased 4.8- and 9.1-fold, respectively, for the 100-μg dosage level. All subjects tested who received the 50- or 100-μg vaccine dose developed immunoglobulin A ASCs. These cells expressed molecules associated with homing to mucosal and peripheral lymphoid tissues.
The intranasal monovalent adjuvanted Norwalk VLP vaccine was well tolerated and highly immunogenic and is a candidate for additional study.
诺如病毒在全球各年龄段人群中均可引起急性肠胃炎,导致较高的发病率和死亡率。
我们进行了两项 1 期、双盲、对照研究,研究对象为一种病毒样颗粒(VLP)疫苗,该疫苗源自诺如病毒 GI.1 基因型,佐剂为单磷酰脂质 A(MPL)和黏膜黏附性壳聚糖。18-49 岁的健康受试者随机分为 2 组,分别接受鼻内诺如病毒 VLP 疫苗或对照疫苗,间隔 21 天接种 2 剂。研究 1 评估了 5-、15-和 50-μg 剂量的诺瓦克抗原,研究 2 评估了 50-和 100-μg 剂量。志愿者在给药后 7 天内记录症状,并在 180 天内随访安全性。采集血样进行血清学分析、抗体分泌细胞(ASC)分析以及 ASC 归巢受体分析。
最常见的症状是鼻塞、流涕和打喷嚏。未发生与疫苗相关的严重不良事件。100μg 剂量水平下,诺瓦克 VLP 特异性 IgG 和 IgA 抗体分别增加了 4.8 倍和 9.1 倍。接受 50μg 或 100μg 疫苗剂量的所有受试者均产生了 IgA ASC。这些细胞表达与黏膜和外周淋巴组织归巢相关的分子。
鼻内单价佐剂诺瓦克 VLP 疫苗具有良好的耐受性和高度的免疫原性,是进一步研究的候选疫苗。