Schwartz Jennifer A, Buonocore Linda, Roberts Anjeanette, Suguitan Amorsolo, Kobasa Darwyn, Kobinger Gary, Feldmann Heinz, Subbarao Kanta, Rose John K
Department of Pathology, Yale University School of Medicine, 310 Cedar St. LH 315, New Haven, CT 06520, USA.
Virology. 2007 Sep 15;366(1):166-73. doi: 10.1016/j.virol.2007.04.021. Epub 2007 May 23.
Given the lethality of H5N1 avian influenza viruses (AIV) and the recurring spread from poultry to humans, an effective vaccine against H5N1 viruses may be needed to prevent a pandemic. We generated experimental vaccine vectors based on recombinant vesicular stomatitis virus (VSV) expressing the H5 hemagglutinin (HA) from an H5N1 virus isolated in 1997. The HA gene was expressed either from an attenuated wild-type VSV vector or from a single-cycle vector containing a deletion of the VSV G gene. We found that all of the vectors induced potent neutralizing antibody titers against the homologous and antigenically heterologous H5N1 viruses isolated in 2004 and 2005. Vaccination of mice with any combination of prime or prime/boost vectors provided long-lasting protection (>7 months) against challenge with AIV, even in animals receiving a single dose of single-cycle vaccine. Our data indicate that these recombinants are promising vaccine candidates for pandemic influenza.
鉴于H5N1禽流感病毒(AIV)的致死性以及其不断从家禽传播至人类的情况,可能需要一种有效的H5N1病毒疫苗来预防大流行。我们基于表达1997年分离的H5N1病毒的H5血凝素(HA)的重组水疱性口炎病毒(VSV)构建了实验性疫苗载体。HA基因可从减毒野生型VSV载体表达,也可从缺失VSV G基因的单周期载体表达。我们发现,所有载体均能诱导针对2004年和2005年分离的同源及抗原性异源H5N1病毒产生高效中和抗体滴度。用任何初免或初免/加强载体组合对小鼠进行疫苗接种,均可为其提供针对AIV攻击的长期保护(>7个月),即使是接受单剂量单周期疫苗的动物也是如此。我们的数据表明,这些重组体是有前景的大流行性流感疫苗候选物。