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免疫缺陷个体中脊髓灰质炎病毒复制28年:对全球根除脊髓灰质炎行动的影响

Twenty-Eight Years of Poliovirus Replication in an Immunodeficient Individual: Impact on the Global Polio Eradication Initiative.

作者信息

Dunn Glynis, Klapsa Dimitra, Wilton Thomas, Stone Lindsay, Minor Philip D, Martin Javier

机构信息

Division of Virology, National Institute for Biological Standards and Control, Potters Bar, Hertfordshire, United Kingdom.

出版信息

PLoS Pathog. 2015 Aug 27;11(8):e1005114. doi: 10.1371/journal.ppat.1005114. eCollection 2015 Aug.

Abstract

There are currently huge efforts by the World Health Organization and partners to complete global polio eradication. With the significant decline in poliomyelitis cases due to wild poliovirus in recent years, rare cases related to the use of live-attenuated oral polio vaccine assume greater importance. Poliovirus strains in the oral vaccine are known to quickly revert to neurovirulent phenotype following replication in humans after immunisation. These strains can transmit from person to person leading to poliomyelitis outbreaks and can replicate for long periods of time in immunodeficient individuals leading to paralysis or chronic infection, with currently no effective treatment to stop excretion from these patients. Here, we describe an individual who has been excreting type 2 vaccine-derived poliovirus for twenty eight years as estimated by the molecular clock established with VP1 capsid gene nucleotide sequences of serial isolates. This represents by far the longest period of excretion described from such a patient who is the only identified individual known to be excreting highly evolved vaccine-derived poliovirus at present. Using a range of in vivo and in vitro assays we show that the viruses are very virulent, antigenically drifted and excreted at high titre suggesting that such chronic excreters pose an obvious risk to the eradication programme. Our results in virus neutralization assays with human sera and immunisation-challenge experiments using transgenic mice expressing the human poliovirus receptor indicate that while maintaining high immunisation coverage will likely confer protection against paralytic disease caused by these viruses, significant changes in immunisation strategies might be required to effectively stop their occurrence and potential widespread transmission. Eventually, new stable live-attenuated polio vaccines with no risk of reversion might be required to respond to any poliovirus isolation in the post-eradication era.

摘要

目前,世界卫生组织及其合作伙伴正在为实现全球消灭脊髓灰质炎付出巨大努力。近年来,由于野生脊髓灰质炎病毒导致的脊髓灰质炎病例大幅下降,与使用口服减毒活疫苗相关的罕见病例变得更加重要。口服疫苗中的脊髓灰质炎病毒株在免疫后于人体中复制后,已知会迅速恢复为神经毒性表型。这些毒株可在人与人之间传播,导致脊髓灰质炎暴发,并且可在免疫缺陷个体中长时间复制,导致瘫痪或慢性感染,目前尚无有效的治疗方法来阻止这些患者排出病毒。在此,我们描述了一名个体,根据用连续分离株的VP1衣壳基因核苷酸序列建立的分子钟估计,该个体已排出2型疫苗衍生脊髓灰质炎病毒长达28年。这是迄今为止已知的此类患者中描述的最长排毒期,该患者是目前唯一被确认正在排出高度进化的疫苗衍生脊髓灰质炎病毒的个体。我们使用一系列体内和体外试验表明,这些病毒具有很强的毒性、抗原性发生了漂移并且以高滴度排出,这表明此类慢性排毒者对消灭计划构成了明显风险。我们用人血清进行病毒中和试验以及使用表达人脊髓灰质炎病毒受体的转基因小鼠进行免疫挑战实验的结果表明,虽然维持高免疫覆盖率可能会对这些病毒引起的麻痹性疾病提供保护,但可能需要对免疫策略进行重大改变,以有效阻止它们的出现和潜在的广泛传播。最终,可能需要新的无回复风险的稳定口服减毒脊髓灰质炎疫苗,以应对消灭脊髓灰质炎后时代的任何脊髓灰质炎病毒分离情况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f55/4552295/e51f77ee3805/ppat.1005114.g001.jpg

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