Publication:
Relapse

dc.contributor.authorNicholas J. Whiteen_US
dc.contributor.authorMallika Imwongen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2018-06-11T04:50:50Z
dc.date.available2018-06-11T04:50:50Z
dc.date.issued2012-12-05en_US
dc.description.abstractPlasmodium vivax is a major cause of febrile illness in endemic areas of Asia, Central and South America, and the horn of Africa. P. vivax infections are characterized by relapses of malaria arising from persistent liver stages of the parasite (hypnozoites), which can be prevented currently only by 8-aminoquinoline anti-malarials. Tropical P. vivax infections relapse at approximately 3-week intervals if rapidly eliminated anti-malarials are given for treatment, whereas in temperate regions and parts of the sub-tropics, P. vivax infections are characterized by either a long incubation or a long-latency period between illness and relapse - in both cases approximating 8-10 months. The epidemiology of the different relapse phenotypes has not been defined adequately despite obvious relevance to malaria therapeutic assessment, control, and elimination. The number of sporozoites inoculated by the anopheline mosquito is an important determinant of both the timing and the number of relapses. The intervals between P. vivax relapses display a remarkable periodicity which has not been explained. Evidence is presented that the proportion of patients who have successive relapses is relatively constant and that the factor which activates hypnozoites and leads to regular interval relapse in vivax malaria is the systemic febrile illness itself. It is proposed that in endemic areas, a large proportion of the population harbours latent hypnozoites which can be activated by a systemic illness such as vivax or falciparum malaria. This explains the high rates of vivax following falciparum malaria, the high proportion of heterologous genotypes in relapses, the higher rates of relapse in people living in endemic areas compared with artificial infection studies, and, by facilitating recombination between different genotypes, contributes to P. vivax genetic diversity particularly in low transmission settings. Long-latency P. vivax phenotypes may be more widespread and more prevalent than currently thought. These observations have important implications for the assessment of radical treatment efficacy and for malaria control and elimination. © 2012 Elsevier Ltd.en_US
dc.identifier.citationAdvances in Parasitology. Vol.80, (2012), 113-150en_US
dc.identifier.doi10.1016/B978-0-12-397900-1.00002-5en_US
dc.identifier.issn0065308Xen_US
dc.identifier.other2-s2.0-84870376266en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/14227
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84870376266&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.titleRelapseen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84870376266&origin=inwarden_US

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