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给红腿鹧鸪注射非结构NS1蛋白后,其对西尼罗河病毒病无保护作用且出现不良反应。

Absence of protection from West Nile virus disease and adverse effects in red legged partridges after non-structural NS1 protein administration.

作者信息

Rebollo Belén, Llorente Francisco, Pérez-Ramírez Elisa, Sarraseca Javier, Gallardo Carmina, Risalde María Ángeles, Höfle Ursula, Figuerola Jordi, Soriguer Ramón C, Venteo Ángel, Jiménez-Clavero Miguel Ángel

机构信息

Inmunología y Genética Aplicada, S.A. (INGENASA), C/Hermanos García Noblejas 39, 28037, Madrid, Spain.

Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria - Centro de Investigación en Sanidad Animal (INIA-CISA), Ctra Algete-El Casar s/n, 208130, Valdeolmos, Madrid, Spain.

出版信息

Comp Immunol Microbiol Infect Dis. 2018 Feb;56:30-33. doi: 10.1016/j.cimid.2017.12.006. Epub 2018 Jan 9.

Abstract

The red-legged partridge (Alectoris rufa) is a competent host for West Nile virus (WNV) replication and highly susceptible to WNV disease. With the aim to assess in this species whether the inoculation of non-structural protein NS1 from WNV elicits a protective immune response against WNV infection, groups of partridges were inoculated with recombinant NS1 (NS1 group) or an unrelated recombinant protein (mock group), and challenged with infectious WNV. A third group received no inoculation prior to challenge (challenge group). The NS1 group failed to elicit detectable antibodies to NS1 while in the mock group a specific antibody response was observed. Moreover, no protection against WNV disease was observed in the NS1 group, but rather, it showed significantly higher viral RNA load and delayed neutralizing antibody response, and suffered a more severe clinical disease, which resulted in higher mortality. This adverse effect has not been observed before and warrants further investigations.

摘要

红腿鹧鸪(Alectoris rufa)是西尼罗河病毒(WNV)复制的适宜宿主,且对WNV疾病高度易感。为评估在该物种中接种WNV非结构蛋白NS1是否能引发针对WNV感染的保护性免疫反应,将几组鹧鸪分别接种重组NS1(NS1组)或无关重组蛋白(模拟组),然后用传染性WNV进行攻毒。第三组在攻毒前未接种(攻毒组)。NS1组未能产生可检测到的针对NS1的抗体,而模拟组则观察到特异性抗体反应。此外,NS1组未观察到对WNV疾病的保护作用,反而显示出病毒RNA载量显著更高、中和抗体反应延迟,且临床疾病更严重,导致死亡率更高。这种不良反应以前未被观察到,值得进一步研究。

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