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商业猪流感疫苗对近期欧洲 H1N1 分离株攻毒的效力。

Efficacy of commercial swine influenza vaccines against challenge with a recent European H1N1 field isolate.

机构信息

Laboratory of Virology, Faculty of Veterinary Medicine, Ghent University, Salisburylaan 133, B-9820 Merelbeke, Belgium.

出版信息

Vet Microbiol. 2010 Jul 29;144(1-2):67-74. doi: 10.1016/j.vetmic.2009.12.039. Epub 2010 Jan 11.

DOI:10.1016/j.vetmic.2009.12.039
PMID:20116942
Abstract

This study examines the immunogenicity and efficacy of four commercial swine influenza (SI) vaccines against challenge with a recent European H1N1 virus, Sw/Gent/112/07. The vaccines contained different H1N1 strains showing between 77% and 95% genetic homology with the haemagglutinin (HA) of the challenge virus. Four groups of 10 pigs each received a double vaccination, with a 4-week interval, with one of the vaccines; a fifth group served as unvaccinated controls. All pigs were challenged 3 weeks after the second vaccination intratracheally with 10(5.0)EID(50) of Sw/Gent/112/07. Sera were examined in haemagglutination inhibition (HI) tests against the homologous vaccine H1N1 strains, the challenge virus and a panel of five recent H1N1 isolates. Pigs were euthanized at 24 or 72h post-challenge and virus titres were determined in right and left lung halves. Two vaccines, in which the H1N1 strains showed a genetic homology of 93% and 89% to Sw/Gent/112/07, significantly reduced virus replication. The vaccine containing an H1N1 strain with 95% homology to Sw/Gent/112/07, did not offer significant protection, neither did it induce the highest HI titres. In general, pigs with HI antibody titres >or=20 against Sw/Gent/112/07 were virologically protected against challenge. HI titres against other viruses, however, differed compared to the challenge virus and between viruses. Our data clearly show that the genetic homology with the challenge virus is not the ultimate predictor for SI vaccine performance. The true reason for the differences in vaccine potency remains obscure because other factors, such as the antigen dose and/or the adjuvant, also differed between the vaccines.

摘要

本研究旨在检验四种市售猪流感(SI)疫苗对近期欧洲 H1N1 病毒 Sw/Gent/112/07 攻毒的免疫原性和效力。这些疫苗包含不同的 H1N1 株,其血凝素(HA)与攻毒病毒的同源性在 77%至 95%之间。每组 10 头猪分为 4 组,每组接受一种疫苗的两次免疫接种,间隔 4 周;第 5 组为未接种疫苗的对照。所有猪在第二次免疫接种后 3 周,通过气管内途径用 10(5.0)EID(50)的 Sw/Gent/112/07 攻毒。在血凝抑制(HI)试验中,用同源疫苗的 H1N1 株、攻毒病毒和一组五种近期的 H1N1 分离株检测血清。攻毒后 24 或 72 小时处死猪,测定右肺和左肺半叶的病毒滴度。两种疫苗的 H1N1 株与 Sw/Gent/112/07 的遗传同源性分别为 93%和 89%,显著降低了病毒复制。含有与 Sw/Gent/112/07 同源性为 95%的 H1N1 株的疫苗,并未提供显著保护,也未诱导最高的 HI 滴度。一般来说,HI 抗体滴度对 Sw/Gent/112/07 为 >或=20 的猪在病毒学上对攻毒具有保护作用。然而,针对其他病毒的 HI 滴度与攻毒病毒不同,并且在不同病毒之间也存在差异。我们的数据清楚地表明,与攻毒病毒的遗传同源性并不是 SI 疫苗效力的最终预测因素。疫苗效力差异的确切原因尚不清楚,因为疫苗之间的抗原剂量和/或佐剂等其他因素也存在差异。

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