A case of Plasmodium falciparum malaria presenting 13 years after leaving an endemic area.

Infectious diseases (London, England) Pub Date : 2025-07-01 Epub Date: 2025-05-13 DOI:10.1080/23744235.2025.2505078
David Hettle, Mustafa Elsayed, Samuel Mensah, Francesca Neuberger, Debbie Nolder, Hristina Vasileva, Kevin Tetteh, Tim Cutfield, Imogen Jones, Spencer Polley, Louise Turner, Thomas Lavstsen, Colin Sutherland, Peter Chiodini, Izak Heys
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Abstract

Plasmodium falciparum usually causes an acute malaria infection, with symptoms presenting from 8 to 11 days onwards following inoculation by an infected mosquito. However, evidence suggesting chronic carriage of blood-stage infection, which can lead to recrudescence of parasitaemia as immunity wanes, has been documented in migrants from malaria-endemic to non-endemic regions. We report the case of a pregnant patient who presented in late 2020 with symptomatic P. falciparum malaria, having lived continuously in areas non-endemic for malaria (Spain and the UK) for 13 years. The patient was originally from Equatorial Guinea but had not visited a malaria-endemic region since leaving Africa in 2007. Serological characterisation of peripheral antibodies circulating 4 months prior to, during and 2 months after the acute malaria episode suggests induction of IgG recognising placental malaria-specific antigens during the pregnancy. These antibodies waned in titre following successful treatment of the acute malaria episode. Immunological recognition of other blood-stage parasite antigens prior to the acute episode was seen, consistent with an ongoing chronic infection, presumably contracted during childhood before the individual left Equatorial Guinea 13 years earlier. This represents one of the longest-documented periods between exposure and eventual clinical presentation with P. falciparum malaria, and the longest described in a pregnant patient. Our findings have implications for eradication programmes and patient care, with the need to consider P. falciparum infection in patients who have migrated to malaria non-endemic settings, particularly those with altered physiological states such as pregnancy, despite absence of a recent travel history to an endemic region.

恶性疟原虫疟疾病例在离开流行地区13年后出现。
恶性疟原虫通常引起急性疟疾感染,在感染蚊子接种后8至11天出现症状。然而,有证据表明,在从疟疾流行地区到非流行地区的移民中存在慢性血期感染,这可能导致寄生虫病在免疫力减弱时复发。我们报告了一名怀孕患者的病例,她在2020年底出现了症状性恶性疟原虫疟疾,她在非疟疾流行地区(西班牙和英国)连续生活了13年。该患者最初来自赤道几内亚,但自2007年离开非洲以来从未去过疟疾流行地区。急性疟疾发作前4个月、发作期间和发作后2个月循环的外周血抗体的血清学特征表明,妊娠期间可诱导IgG识别胎盘疟疾特异性抗原。在成功治疗急性疟疾发作后,这些抗体呈滴度下降。在急性发作之前,观察到对其他血期寄生虫抗原的免疫识别,这与持续的慢性感染相一致,可能是在个体13年前离开赤道几内亚之前的童年时期感染的。这是从接触到最终临床表现为恶性疟原虫疟疾之间记录时间最长的时期之一,也是怀孕患者中记录时间最长的。我们的研究结果对根除疟疾规划和患者护理具有重要意义,需要考虑迁移到疟疾非流行地区的患者的恶性疟原虫感染,特别是那些生理状态发生改变(如怀孕)的患者,尽管近期没有前往流行地区的旅行史。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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