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针对猫免疫缺陷病毒的实验性疫苗保护作用。

Experimental vaccine protection against feline immunodeficiency virus.

作者信息

Yamamoto J K, Okuda T, Ackley C D, Louie H, Pembroke E, Zochlinski H, Munn R J, Gardner M B

机构信息

Department of Medicine, School of Veterinary Medicine, University of California, Davis 95616.

出版信息

AIDS Res Hum Retroviruses. 1991 Nov;7(11):911-22. doi: 10.1089/aid.1991.7.911.

Abstract

Infection of domestic cats with the feline immunodeficiency virus (FIV) represents an important veterinary health problem and a useful animal model for the development of vaccines against acquired immunodeficiency syndrome (AIDS). Two experimental FIV vaccines have been developed; one consisting of fixed infected cells (Vaccine 1), the other of inactivated whole virus (Vaccine 2). After 4-6 immunizations over 2-5 months, both vaccines induced a strong FIV-specific immune response including neutralizing antibody and T-cell proliferation. Vaccine 1 protected 6 of 9 and Vaccine 2 protected 5 of 6 recipient cats against any detectable infection with a low dose (10 animal ID50) of FIV given intraperitoneally 2 weeks after the final boost. One additional cat in each vaccine group had a transient infection at 5-7 weeks postchallenge following which virus could no longer be detected. Thus, a total of 13 of 15 vaccinated cats were protected against persistent infection. By contrast, 13 of 13 controls were persistently infected by this challenge. The infected cell vaccine failed to protect against a higher dose (5 x 10(4) ID50) of FIV. These results indicate that vaccine prophylaxis against natural FIV infection should be achievable and enhance optimism of the prospect of developing an effective AIDS vaccine for humans.

摘要

家猫感染猫免疫缺陷病毒(FIV)是一个重要的兽医健康问题,也是开发抗获得性免疫缺陷综合征(AIDS)疫苗的有用动物模型。已开发出两种实验性FIV疫苗;一种由固定感染细胞组成(疫苗1),另一种由灭活全病毒组成(疫苗2)。在2至5个月内进行4至6次免疫后,两种疫苗均诱导了强烈的FIV特异性免疫反应,包括中和抗体和T细胞增殖。在最后一次加强免疫后2周,腹腔注射低剂量(10个动物半数感染量)的FIV,疫苗1保护了9只受者猫中的6只,疫苗2保护了6只受者猫中的5只免受任何可检测到的感染。每个疫苗组中另外有1只猫在攻毒后5至7周出现短暂感染,此后病毒检测不到。因此,15只接种疫苗的猫中共有13只受到保护,免受持续感染。相比之下,13只对照猫均被此次攻毒持续感染。感染细胞疫苗不能保护猫免受更高剂量(5×10⁴半数感染量)的FIV感染。这些结果表明,预防自然FIV感染的疫苗应该是可以实现的,并增强了开发人类有效AIDS疫苗前景的乐观情绪。

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