Intercell AG, Campus Vienna Biocenter 3, 1030 Wien, Austria.
Vaccine. 2010 Sep 7;28(39):6463-9. doi: 10.1016/j.vaccine.2010.07.040. Epub 2010 Jul 29.
Japanese encephalitis (JE) is the most common viral encephalitis in Asia. IXIARO is a Vero cell-derived, inactivated JE virus vaccine which has recently been approved in the US, Europe, Canada and Australia (trade name JESPECT). This overview of the safety and tolerability of IXIARO, for 6 months after the first vaccination in 7 Phase III trials, includes: 3558 subjects with at least one IXIARO vaccination, 435 subjects with a JE-VAX (manufactured by BIKEN, distributed by Sanofi Pasteur) vaccination, and 657 with phosphate-buffered saline solution with 0.1% Al(OH)(3) (PBS+Alum) control vaccination. The percentage of subjects reporting solicited local adverse events (AEs) with IXIARO (54%) was similar to PBS+Alum vaccination (56%) as were solicited systemic adverse events (40% IXIARO; 40% PBS+Alum vaccination). JE-VAX showed a higher frequency of subjects with solicited local adverse events (61%) but a slightly lower frequency of subjects with solicited systemic adverse events (36%). The frequency of subjects with any solicited and unsolicited AE with IXIARO (64%) was also similar to PBS+Alum vaccination (61%) and JE-VAX (64%); as for subjects with serious AEs (1% IXIARO; 2% PBS+Alum vaccination, 1% JE-VAX). No serious allergic reactions were observed in any group. This safety analysis indicates that IXIARO has a favorable safety profile, comparable to PBS+Alum control vaccination and appears to have a better local tolerability profile than JE-VAX.
日本脑炎(JE)是亚洲最常见的病毒性脑炎。IXIARO 是一种由 Vero 细胞衍生的、已灭活的 JE 病毒疫苗,最近已在美国、欧洲、加拿大和澳大利亚获得批准(商品名 JESPECT)。这项对 7 项 III 期临床试验中首次接种后 6 个月内 IXIARO 的安全性和耐受性的概述,包括:至少接种了 1 剂 IXIARO 的 3558 名受试者、435 名接种了 JE-VAX(由 BIKEN 生产,由 Sanofi Pasteur 分销)的受试者和 657 名接受磷酸盐缓冲盐水与 0.1%Al(OH)(3)(PBS+Alum)对照疫苗接种的受试者。报告有局部不良事件(AE)的受试者百分比(IXIARO 为 54%)与 PBS+Alum 疫苗接种(56%)相似,全身性不良事件(IXIARO 为 40%;PBS+Alum 疫苗接种为 40%)也是如此。JE-VAX 组报告有局部不良事件的受试者频率更高(61%),但报告有全身性不良事件的受试者频率略低(36%)。报告有任何局部和全身不良事件的受试者频率(IXIARO 为 64%)与 PBS+Alum 疫苗接种(61%)和 JE-VAX(64%)相似;至于报告有严重不良事件的受试者(IXIARO 为 1%;PBS+Alum 疫苗接种为 2%,JE-VAX 为 1%)。任何组均未观察到严重过敏反应。这项安全性分析表明,IXIARO 具有良好的安全性,与 PBS+Alum 对照疫苗接种相当,并且似乎比 JE-VAX 具有更好的局部耐受性。