Publications by authors named "Rhea Longley"

Article Synopsis
  • This study investigates the effectiveness and safety of different primaquine dosing strategies in preventing relapsing Plasmodium vivax malaria in children under 15 years.
  • A systematic review was conducted, analyzing various studies involving children treated with primaquine, focusing on those who received treatment over multiple days and were followed up for at least 28 days.
  • The findings from 3514 children across 27 studies were compiled to analyze different dosing regimens, assess the risk of recurrent malaria, and evaluate tolerability and safety concerning adverse effects.
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  • - Over the past few decades, malaria cases in Cambodia have decreased significantly, leading to fragmented transmission in remote areas, prompting a study to examine the burden of Plasmodium infections near the forest regions in Mondulkiri.
  • - The study involved 950 participants from 2018 to 2020, where blood samples were tested for Plasmodium infections and a risk analysis was conducted. It found that living in the forest greatly increased the risk of infection, particularly in adult males.
  • - Results indicated that baseline serological status (whether participants tested positive or negative) was a strong predictor of future infections, stressing the need for targeted serological testing to effectively address malaria risks, especially in demographics living outside forest areas.
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Background: Imperfect adherence is a major barrier to effective primaquine radical cure of Plasmodium vivax. This study investigated the effect of reduced adherence on the risk of P. vivax recurrence.

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Background: Primaquine is used to eliminate Plasmodium vivax hypnozoites, but its optimal dosing regimen remains unclear. We undertook a systematic review and individual patient data meta-analysis to investigate the efficacy and tolerability of different primaquine dosing regimens to prevent P vivax recurrence.

Methods: For this systematic review and individual patient data meta-analysis, we searched MEDLINE, Web of Science, Embase, and Cochrane Central for prospective clinical studies of uncomplicated P vivax from endemic countries published between Jan 1, 2000, and June 8, 2023.

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The utilisation of serological surveillance methods for malaria has the potential to identify individuals exposed to , including asymptomatic carriers. However, the application of serosurveillance varies globally, including variations in methodology and transmission context. No systematic review exists describing the advantages and disadvantages of utilising serosurveillance in various settings.

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Article Synopsis
  • As malaria elimination efforts advance, the challenges from certain parasite species are becoming clearer, especially as the proportion of cases caused by these parasites rises in co-endemic regions.
  • There is currently no advanced vaccine for these specific malaria parasites, and only a few candidates are in development.
  • This study screened 342 proteins to find promising candidates for a subunit vaccine, confirming two known protective proteins and discovering at least four new candidates that may offer similar protective benefits.
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Background: Pregnant women have increased susceptibility to Plasmodium falciparum malaria and acquire protective antibodies over successive pregnancies. Most studies that investigated malaria antibody responses in pregnant women are from high transmission areas in sub-Saharan Africa, while reports from Latin America are scarce and inconsistent. The present study sought to explore the development of antibodies against P.

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Background: To make progress towards malaria elimination, a highly effective vaccine targeting Plasmodium vivax is urgently needed. Evaluating the kinetics of natural antibody responses to vaccine candidate antigens after acute vivax malaria can inform the design of serological markers of exposure and vaccines.

Methodology/principal Findings: The responses of IgG antibodies to 9 P.

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A more sensitive surveillance tool is needed to identify infections for treatment and to accelerate malaria elimination efforts. To address this challenge, our laboratory has developed an eight-antigen panel that detects total IgG as serological markers of exposure within the prior 9 months. The value of these markers has been established for use in areas with low transmission.

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Serological markers are a promising tool for surveillance and targeted interventions for Plasmodium vivax malaria. P. vivax is closely related to the zoonotic parasite P.

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Background: Plasmodium vivax is emerging as the dominant and prevalent species causing malaria in near-elimination settings outside of Africa. Hypnozoites, the dormant liver stage parasite of P. vivax, are undetectable to any currently available diagnostic test, yet are a major reservoir for transmission.

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Plasmodium vivax is the most widespread causative agent of human malaria in the world. Despite the ongoing implementation of malaria control programs, the rate of case reduction has declined over the last 5 years. Hence, surveillance of malaria transmission should be in place to identify and monitor areas that require intensified malaria control interventions.

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Serology tests are extremely useful for assessing whether a person has been infected with a pathogen. Since the onset of the COVID-19 pandemic, measurement of anti-SARS-CoV-2-specific antibodies has been considered an essential tool in identifying seropositive individuals and thereby understanding the extent of transmission in communities. The Luminex system is a bead-based technology that has the capacity to assess multiple antigens simultaneously using very low sample volumes and is ideal for high-throughput studies.

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The rotating-crystal magneto-optical detection (RMOD) method has been developed for the rapid and quantitative diagnosis of malaria and tested systematically on various malaria infection models. Very recently, an extended field trial in a high-transmission region of Papua New Guinea demonstrated its great potential for detecting malaria infections, in particular Plasmodium vivax. In the present small-scale field test, carried out in a low-transmission area of Thailand, RMOD confirmed malaria in all samples found to be infected with Plasmodium vivax by microscopy, our reference method.

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Thailand is aiming for malaria elimination by the year 2030. However, the high proportion of asymptomatic infections and the presence of the hidden hypnozoite stage of are impeding these efforts. We hypothesized that a validated surveillance tool utilizing serological markers of recent exposure to infection could help to identify areas of ongoing transmission.

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Article Synopsis
  • New tools are essential for malaria elimination, specifically targeting recent exposure to the disease.
  • A novel panel of proteins was identified as serological markers to detect exposure within the last 9 months.
  • The study compared IgM and IgG antibody responses using plasma samples from malaria-endemic regions, finding that IgM responses were less effective in classifying exposure than IgG.
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Article Synopsis
  • * R21, when combined with Matrix-M, demonstrated strong immune responses and full protection against malaria challenges, and initial results suggest that lower doses of both R21 and RTS,S in AS01 may enhance immunity and protection.
  • * The research indicates that combining RTS,S with TRAP-based viral vectors may lead to improved immune responses without significant interference, highlighting the potential for multi-component vaccination strategies and the importance of testing low-dose vaccines in humans.
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Background: Antibody responses as serological markers of Plasmodium vivax infection have been shown to correlate with exposure, but little is known about the other factors that affect antibody responses in naturally infected people from endemic settings. To address this question, we studied IgG responses to novel serological exposure markers (SEMs) of P. vivax in three settings with different transmission intensity.

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Background: Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) induces an antibody response targeting multiple antigens that changes over time. This study aims to take advantage of this complexity to develop more accurate serological diagnostics.

Methods: A multiplex serological assay was developed to measure IgG and IgM antibody responses to seven SARS-CoV-2 spike or nucleoprotein antigens, two antigens for the nucleoproteins of the 229E and NL63 seasonal coronaviruses, and three non-coronavirus antigens.

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Multiplexed bead-based assays that use Luminex® xMAP® technology have become popular for measuring antibodies against proteins of interest in many fields, including malaria and more recently SARS-CoV-2/COVID-19. There are currently two formats that are widely used: non-magnetic beads or magnetic beads. Data are lacking regarding the comparability of results obtained using these two types of beads, and for assays run on different instruments.

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Article Synopsis
  • There is a significant gap in identifying individuals with silent liver-stage parasites called hypnozoites in the context of Plasmodium vivax elimination efforts.
  • The study created a panel of serological markers to help identify those with recent P. vivax infections who are likely carrying hypnozoites, relying on measurements of IgG antibody responses to numerous P. vivax proteins.
  • Validation of these markers showed that they can accurately classify recent infections with about 80% sensitivity and specificity, and a model suggests that implementing serological testing could significantly lower P. vivax prevalence by 59-69%.
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Purpose: Pharmacogenes have an influence on biotransformation pathway and clinical outcome of primaquine and chloroquine which are often prescribed to treat infection. Genetic variation may impact enzyme activity and/or transporter function and thereby contribute to relapse. The aim of the study was to assess allele, genotype frequencies and the association between pharmacogenes variation and primaquine response in Thai patients infected with .

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Despite promising progress in malaria vaccine development in recent years, an efficacious subunit vaccine against remains to be licensed and deployed. Cell-mediated protection from liver-stage malaria relies on a sufficient number of antigen-specific T cells reaching the liver during the time that parasites are present. A single vaccine expressing two antigens could potentially increase both the size and breadth of the antigen-specific response while halving vaccine production costs.

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