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首页> 外文期刊>Vaccine >Safety and immunogenicity of an influenza vaccine A/H5N1 (A/Vietnam/1194/2004) when coadministered with a heat-labile enterotoxin (LT) adjuvant patch
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Safety and immunogenicity of an influenza vaccine A/H5N1 (A/Vietnam/1194/2004) when coadministered with a heat-labile enterotoxin (LT) adjuvant patch

机译:流感疫苗A / H5N1(A / Vietnam / 1194/2004)与热不稳定肠毒素(LT)佐剂贴片同时使用时的安全性和免疫原性

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Background: The use of adjuvants to enhance the immune response to novel pandemic influenza vaccine candidates may overcome the poor immune responses seen in immunologically naive populations. The confluence of a highly pathogenic H5N1 influenza virus and the widespread absence of pre-existing immunity has driven the search for effective strategies for immunization in the face of a lethal pandemic. The potent adjuvant, heat labile enterotoxin from E, coli (LT), placed over the immunization site in a patch, is a novel adjuvant strategy for immune enhancement, and was evaluated using an H5N1 injectable vaccine.Methods: In this observer-blind, placebo-controlled clinical study, 500 healthy adults 18-49 years of age were randomized to receive two intramuscular doses of A/Vietnam/1194/2004 A/H5N1 vaccine (5 mu g, 15 mu g or 45 mu g) or placebo (saline) 21 days apart. For each of the influenza vaccine doses, a 50 mu g LT adjuvant patch was applied over the injection site at either the second or both immunizations and the HI responses (titers) were compared to H5N1 vaccine alone. The study's primary endpoint was safety, and secondary immunogenicity endpoints were evaluated using European (CHMP) licensure criteria.Results: The vaccine was safe and well tolerated, and subjects generally lacked pre-existing H5N1 immunity. The single-dose injection 45 mu g HA/LT patch regimen met all CHMP licensure criteria, including a 73% seroprotection rate compared to 49% seroprotection without a patch. Significant adjuvant effects were seen at all HA doses on Day 21. By contrast, only modest adjuvant effects were observed with the boosting regimen in subjects first primed with H5N1 alone and given the adjuvant patch only on the second immunization. The two-injection/two-patch 45 mu g HA regimen achieved significantly higher titers and GMFR compared to injection alone (GMFR 33.1 vs. 16.9. HI 226 vs. 94, p < 0.05) and a 94% seroprotection rate.Conclusions: The LT adjuvant patch placed over the injection site was safe, significantly enhanced the immune response to an H5N1 candidate vaccine, and achieved a 73% seroprotection rate after a single dose. The LT adjuvant patch has more modest benefits in recently primed populations similar to other candidate vaccine adjuvants, but a two-dose patch plus injection regimen resulted in robust HI responses.
机译:背景:使用佐剂增强对新型大流行性流感疫苗候选者的免疫反应可以克服在免疫学纯真的人群中看到的不良免疫反应。高致病性H5N1流感病毒的融合和广泛存在的既有免疫力,促使人们在面对致命的大流行时寻求有效的免疫策略。一种有效的佐剂,来自大肠杆菌的耐热肠毒素(LT),位于补丁的免疫部位上,是一种新的增强免疫的佐剂策略,并使用H5N1可注射疫苗进行了评估。安慰剂对照的临床研究,将500例18-49岁的健康成年人随机接受两次肌肉注射A /越南/ 1194/2004 A / H5N1疫苗(5微克,15微克或45微克)或安慰剂(盐水)相隔21天。对于每种流感疫苗剂量,在第二次免疫或两次免疫时,在注射部位均使用50μg LT佐剂贴片,并将HI应答(滴度)与单独的H5N1疫苗进行比较。该研究的主要终点为安全性,并使用欧洲(CHMP)许可标准对次要免疫原性终点进行了评估。结果:该疫苗安全且耐受性良好,受试者通常缺乏预先存在的H5N1免疫力。单剂量注射45μg HA / LT贴剂方案符合所有CHMP许可标准,包括73%的血清保护率,而没有贴剂的49%血清保护率。在第21天,在所有HA剂量下均观察到显着的佐剂作用。相比之下,在首次单独用H5N1引发并且仅在第二次免疫中给予佐剂贴剂的受试者中,加强方案仅观察到中等佐剂作用。与单独注射相比,两次注射/两次贴剂45μg HA方案的滴度和GMFR显着更高(GMFR 33.1比16.9.HI 226比94,p <0.05)和94%的血清保护率。放置在注射部位的LT佐剂贴剂是安全的,可以显着增强对H5N1候选疫苗的免疫反应,单剂给药后的血清保护率为73%。与其他候选疫苗佐剂相似,LT佐剂贴剂在最近初次接种的人群中具有更适度的益处,但是两剂贴剂加注射方案可产生强劲的HI反应。

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