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Plasmodium falciparum parasites lacking histidine-rich protein 2 and 3: a review and recommendations for accurate reporting

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TLDR
In this paper, the available evidence and molecular basis for identifying malaria parasites lacking the PfHRP2 protein, the most common target antigen for detection of P. falciparum, have been reviewed.
Abstract
Malaria rapid diagnostic tests (RDTs) play a critical role in malaria case management, surveillance and case investigations. Test performance is largely determined by design and quality characteristics, such as detection sensitivity, specificity, and thermal stability. However, parasite characteristics such as variable or absent expression of antigens targeted by RDTs can also affect RDT performance. Plasmodium falciparum parasites lacking the PfHRP2 protein, the most common target antigen for detection of P. falciparum, have been reported in some regions. Therefore, accurately mapping the presence and prevalence of P. falciparum parasites lacking pfhrp2 would be an important step so that RDTs targeting alternative antigens, or microscopy, can be preferentially selected for use in such regions. Herein the available evidence and molecular basis for identifying malaria parasites lacking PfHRP2 is reviewed, and a set of recommended procedures to apply for future investigations for parasites lacking PfHRP2, is proposed.

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REASSURED diagnostics to inform disease control strategies, strengthen health systems and improve patient outcomes

TL;DR: A Perspective discussing the factors that have contributed to the success and failure of point-of-care tests for resource-limited settings and the challenges and opportunities that exist for developing new infectious disease diagnostics.
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Changes in Malaria Epidemiology in Africa and New Challenges for Elimination

TL;DR: Large-scale, robust surveillance mechanisms that measure rather than estimate the actual burden of malaria over time from large areas of the continent where such data are lacking need to be prioritized.
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Major Threat to Malaria Control Programs by Plasmodium falciparum Lacking Histidine-Rich Protein 2, Eritrea.

TL;DR: In this paper, the authors investigated the HRP gene 2/3 status in 50 infected patients at 2 hospitals in Eritrea and found that 80.8% of patients at Ghindae Hospital and 41.7% at Massawa Hospital were infected with pfhrp2-negative parasites and 92.3% (24/26).
References
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Journal ArticleDOI

Genetic Diversity of Plasmodium falciparum Histidine-Rich Protein 2 (PfHRP2) and Its Effect on the Performance of PfHRP2-Based Rapid Diagnostic Tests

TL;DR: The genetic diversity of PfHRP2, which includes numerous amino acid repeats, is examined to provide an alternative explanation for the variable sensitivity in field tests of malaria RDTs that is not due to the quality of the RDT

Malaria rapid diagnostic test performance : results of WHO product testing of malaria RDTs : round 5 (2013)

TL;DR: In 2012, there were an estimated 207 million cases (with an uncertainty range of 135 million to 287 million) and an estimated 627 000 deaths as discussed by the authors, and approximately 90% of all malaria deaths occur in sub-Saharan Africa, and 77% occur in children under 5 years.
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False-Negative Rapid Diagnostic Tests for Malaria and Deletion of the Histidine-Rich Repeat Region of the hrp2 Gene

TL;DR: The results show that parasites that fail to produce HRP2 can cause patent bloodstream infections and false-negative RDT results, and suggest that the use ofHRP2-based RDTs should be reconsidered.
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