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DNA 免疫接种可潜在逆转并预防寨卡病毒引起的雄性小鼠不育症。

Zika-Induced Male Infertility in Mice Is Potentially Reversible and Preventable by Deoxyribonucleic Acid Immunization.

机构信息

Département de Microbiologie-Infectiologie et d'Immunologie, Université Laval, Québec, Canada.

Centre de Recherche en Infectiologie du CHU de Québec - Université Laval, Canada.

出版信息

J Infect Dis. 2019 Jan 9;219(3):365-374. doi: 10.1093/infdis/jiy336.

DOI:10.1093/infdis/jiy336
PMID:30053014
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6325345/
Abstract

BACKGROUND

Zika virus (ZIKV) infection has been associated with prolonged viral excretion in human semen and causes testicular atrophy and infertility in 10-week-old immunodeficient mice.

METHODS

Male IFNAR-/- mice, knockout for type I interferon receptor, were immunized with GLS-5700, a deoxyribonucleic acid-based vaccine, before a subcutaneous ZIKV challenge with 6 × 105 plaque-forming units at 13 weeks of age. On day 28 postinfection, testes and epididymides were collected in some mice for histological and functional analyses, whereas others were mated with naive female wild-type C57BL/6J.

RESULTS

Although all mice challenged with ZIKV developed viremia, most of them were asymptomatic, showed no weight loss, and survived infection. On day 28 postinfection, none of the unvaccinated, infected mice (9 of 9) exhibited abnormal spermatozoa counts or motility. However, 33% (3 of 9) and 36% (4 of 11) of mated males from this group were infertile, from 2 independent studies. Contrarily, males from the noninfected and the vaccinated, infected groups were all fertile. On days 75 and 207 postinfection, partial recovery of fertility was observed in 66% (2 of 3) of the previously infertile males.

CONCLUSIONS

This study reports the effects of ZIKV infection on male fertility in a sublethal, immunodeficient mouse model and the efficacy of GLS-5700 vaccination in preventing male infertility.

摘要

背景

寨卡病毒(ZIKV)感染与人类精液中病毒的长期排泄有关,并导致 10 周龄免疫缺陷小鼠睾丸萎缩和不育。

方法

雄性 IFNAR-/-小鼠,I 型干扰素受体缺失,在 13 周龄时用 GLS-5700(一种基于脱氧核糖核酸的疫苗)进行免疫接种,然后进行皮下 ZIKV 挑战,剂量为 6×105 空斑形成单位。在感染后第 28 天,一些小鼠收集睾丸和附睾进行组织学和功能分析,而另一些则与未感染的野生型 C57BL/6J 雌性小鼠交配。

结果

尽管所有接受 ZIKV 挑战的小鼠都出现病毒血症,但大多数无症状,没有体重减轻,并存活感染。在感染后第 28 天,未接种、感染的小鼠(9 只中的 9 只)没有出现异常的精子计数或活力。然而,该组中 33%(9 只中的 3 只)和 36%(11 只中的 4 只)的交配雄性不育,来自 2 项独立研究。相比之下,来自未感染和接种、感染组的雄性都是可育的。在感染后第 75 天和 207 天,之前不育的雄性中 66%(3 只中的 2 只)观察到部分生育能力恢复。

结论

本研究报告了寨卡病毒感染对亚致死性免疫缺陷小鼠模型中雄性生育力的影响,以及 GLS-5700 疫苗预防雄性不育的疗效。

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DNA vaccination protects mice against Zika virus-induced damage to the testes.DNA 疫苗可保护小鼠免受寨卡病毒引起的睾丸损伤。
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