来自亚洲的人类新(旧)第五疟疾疟原虫

S. Sabbatani, S. Fiorino, R. Manfredi
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引用次数: 0

摘要

在马来西亚过去十年发生的小型流行疫点中发现了一种新型人类疟疾诺氏疟原虫。基于对现有文献资料的回顾,作者强调了用诺氏疟原虫特异性引物进行分子生物学检查的诊断重要性,因为标准的血镜检查可能无法区分诺氏疟原虫和疟疾疟原虫,因为它们的外观相似。据报道,诺氏疟原虫是危及生命甚至致命形式疟疾的一种致病寄生虫。在人类中,与疟疾疟原虫相比,该病的临床表现更为严重,因为该病的特点是寄生率高于疟疾疟原虫。诺氏疟原虫最有效的传播媒介是白纹按蚊,人类和猴子都能吸引它。在灵长类动物中,迄今为止已知诺氏疟原虫的天然宿主,代表它们的是麻花猕猴和nemestina猕猴,而其他猴子,包括猕猴和mulatta猕猴,则不会被感染。这些可能在最终的实验模型中有用。面对诺氏疟原虫对人类疾病的潜在严重演变,我们注意到及时的疾病识别所起的关键作用,这种识别在高风险流行国家的随访患者中可能更容易和明显,但对于出现一些典型疟疾体征和症状的西方国家返回卫生保健服务的受试者应谨慎实施。在东南亚旅行后,他们在热带森林中逗留或短途旅行。对于这些最后的病例,诊断和治疗都应及时、及时和适当。根据文献资料,在非严重的人类病例中,旧的和微不足道的氯喹对诺氏疟原虫仍然非常有效,96%的病例在药物治疗的第一天内症状和体征消失。根据新出现的流行病学数字,诺氏疟原虫被列入间日疟原虫、卵形疟原虫、疟疾疟原虫和恶性疟原虫之后,成为人类疟疾的第五大病原体。在今后几年中,必须规划一项适当的监测方案,监测这种新型人类疟疾的流行病学演变,同时最大限度地关注诺氏疟原虫感染患者的临床表现,根据出现早期体征和症状的时间,预计这些患者的临床病程将更为严重。一些初步的临床数据表明,更严重的情况与寄生虫血症的增加有关,并与寄生虫的人际传播增加相对应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
From Asia, the Novel (and Old) Fifth Malaria Plasmodium of Human Beings
A novel form of human malaria Plasmodium knowlesi has been identified in small epidemic foci occurred during the last decade in Malaysia. Based on a review of the available literature data, the Authors underline the diagnostic importance of molecular biology examinations performed with primers which are specific of Plasmodium knowlesi, since the standard hemoscopy may fail in distinguishing Plasmodium knowlesi from Plasmodium malariae, due to their similar appearance. P. knowlesi has been reported as a causative parasite agent of life-threatening and even lethal forms of malaria. In humans, its clinical picture is more severe a compared to that of P. malariae, since the disease is characterized by a greater parasitemia, versus that is referred in the course of P. malariae disease. The most effective carrier of P. knowlesi is represented by the mosquito Anopheles leucosphyrus, which is attracted by both humans and monkeys. Among primates, the natural hosts of P. Knowlesi are known until now and have been represented by Macaca fascicularis and Macaca nemestina, while other monkeys including Saimiri scirea and Macaca mulatta, which cannot become infected. These might be useful in eventual experimental models. When facing the potentially severe evolution of human disease by P. knowlesi, we remark the key role played by a prompt disease recognition, which is expected to be more easy and obvious in patients followed in endemic countries at elevate risk, but should be carefully implemented for subjects coming back to health care services of western countries, presenting with a number of typical signs and symptoms of malaria, after travelling in South-East Asia where they were engaged in staying or making excursions in the tropical forest. In these last cases, both diagnosis and treatment should be prompt, timely, and appropriate. According to literature data, in non-severe human cases the old and trivial chloroquine remained very effective against P. knowlesi, achieving the disappearance of signs and symptoms in 96% of cases within the first day of pharmacological therapy. On the ground of the emerging epidemiological figures, P. knowlesi was added to Plasmodium vivax, Plasmodium ovale, Plasmodium malariae, and Plasmodium falciparum, as the fifth etiological agent of human malaria. During the next years, it will become mandatory to plan an adequate surveillance programme of the epidemiological evolution of this novel form of human malaria, paying also maximum attention to the clinical presentation of patients affected by P. knowlesi malaria, which are expected to suffer from a more severe clinical course, according to the time elapsed from the appearance of the early signs and symptoms. Some preliminary clinical figures suggest that a greater severity is related to an increased parasitemia, and parallels the increased interhuman infectious passages of parasites.
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