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基于自体感染细胞的实验性猫免疫缺陷病毒疫苗接种会引发同源攻击感染的增强。

Vaccination with experimental feline immunodeficiency virus vaccines, based on autologous infected cells, elicits enhancement of homologous challenge infection.

作者信息

Karlas J A, Siebelink K H, Peer M A, Huisman W, Cuisinier A M, Rimmelzwaan G F, Osterhaus A D

出版信息

J Gen Virol. 1999 Mar;80 ( Pt 3):761-765. doi: 10.1099/0022-1317-80-3-761.

Abstract

Cats were vaccinated with fixed autologous feline immunodeficiency virus (FIV)-infected cells in order to present viral proteins to the immune system of individual cats in an MHC-matched fashion. Upon vaccination, a humoral response against Gag was induced. Furthermore, virus-neutralizing antibodies were detected in a Crandell feline kidney cell-based neutralization assay, but not in a neutralization assay based on primary peripheral blood mononuclear cells. Despite the induction of these FIV-specific responses, vaccinated cats were not protected. Instead, accelerated virus replication was found, an observation similar to what previous experiments using other vaccine candidates have shown. Here, the results of the present study are discussed in the light of enhancement of lentivirus infections as a complicating factor in lentivirus vaccine development.

摘要

猫被接种固定的自体感染猫免疫缺陷病毒(FIV)的细胞,以便以主要组织相容性复合体(MHC)匹配的方式将病毒蛋白呈递给个体猫的免疫系统。接种疫苗后,诱导了针对Gag的体液反应。此外,在基于克兰德尔猫肾细胞的中和试验中检测到病毒中和抗体,但在基于原代外周血单核细胞的中和试验中未检测到。尽管诱导了这些FIV特异性反应,但接种疫苗的猫并未受到保护。相反,发现病毒复制加速,这一观察结果与之前使用其他候选疫苗的实验结果相似。在此,根据慢病毒感染增强作为慢病毒疫苗开发中的一个复杂因素来讨论本研究的结果。

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