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Prime-boost vaccination using DNA and whole inactivated virus vaccines provides limited protection against virulent feline immunodeficiency virus

机译:使用DNA和完整灭活的病毒疫苗的初免-加强疫苗接种提供了针对强毒猫免疫缺陷病毒的有限保护

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Protection against feline immunodeficiency virus (FIV) has been achieved using a variety of vaccines notably whole inactivated virus (WIV) and DNA. However protection against more virulent isolates, typical of those encountered in natural infections, has been difficult to achieve. In an attempt to improve protection against virulent FIV(GL8), we combined both DNA and WIV vaccines in a "prime-boost" approach. Thirty cats were divided into four groups receiving vaccinations and one unvaccinated control group. Following viral challenge, two vaccinated animals, one receiving DNA alone and one the prime-boost vaccine remained free of viraemia, whilst all controls became viraemic. Animals vaccinated with WIV showed apparent early enhancement of infection at 2 weeks post challenge (pc) with higher plasma viral RNA loads than control animals or cats immunised with DNA alone. Despite this, animals vaccinated with WIV or DNA alone showed significantly lower proviral loads in peripheral blood mononuclear cells and mesenteric lymph node cells, whilst those receiving the DNA-WIV prime-boost vaccine showed significantly lower proviral loads in PBMC, than control animals, at 35 weeks pc. Therefore both DNA and WIV vaccines conferred limited protection against viral challenge but the combination of WIV and DNA in a prime-boost approach appeared to offer no significant advantage over either vaccine alone.
机译:使用多种疫苗,尤其是全灭活病毒(WIV)和DNA,已经实现了针对猫免疫缺陷病毒(FIV)的保护。然而,很难获得针对更具毒性的分离株的保护,这些分离株是自然感染中常见的分离株。为了改善针对强毒FIV(GL8)的保护,我们以“初次加强”方法结合了DNA和WIV疫苗。 30只猫分为接受疫苗接种的四组和未接种疫苗的对照组。病毒攻击后,两只疫苗接种的动物,一只单独接受DNA,一只初免-加强疫苗保持无病毒血症,而所有对照都变成病毒血症。与单独用DNA免疫的对照动物或猫相比,接种WIV的动物在攻击后2周表现出明显的早期感染增强,血浆病毒RNA负荷更高。尽管如此,仅接种WIV或DNA的动物在外周血单核细胞和肠系膜淋巴结细胞中的前病毒负荷显着降低,而接受DNA-WIV初免增强疫苗的动物的PBMC中的前病毒负荷显着低于对照动物。 35周因此,DNA和WIV疫苗都针对病毒攻击提供了有限的保护,但是以初免-加强方法结合WIV和DNA似乎没有提供比单独使用任何疫苗明显的优势。

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