Publication:
A new highly sensitive enzyme-linked immunosorbent assay for the detection of Plasmodium falciparum histidine-rich protein 2 in whole blood

dc.contributor.authorIhn Kyung Jangen_US
dc.contributor.authorSmita Dasen_US
dc.contributor.authorRebecca S. Barneyen_US
dc.contributor.authorRoger B. Pecken_US
dc.contributor.authorAndrew Rashiden_US
dc.contributor.authorStephane Prouxen_US
dc.contributor.authorEmmanuel Arinaitween_US
dc.contributor.authorJohn Reken_US
dc.contributor.authorMaxwell Murphyen_US
dc.contributor.authorKatherine Bowersen_US
dc.contributor.authorSamuel Boadien_US
dc.contributor.authorJulie Watsonen_US
dc.contributor.authorFrancois Nostenen_US
dc.contributor.authorBryan Greenhouseen_US
dc.contributor.authorPeter L. Chiodinien_US
dc.contributor.authorGonzalo J. Domingoen_US
dc.contributor.otherInfectious Diseases Research Collaborationen_US
dc.contributor.otherLondon School of Hygiene & Tropical Medicineen_US
dc.contributor.otherPATH Seattleen_US
dc.contributor.otherUniversity of California, San Franciscoen_US
dc.contributor.otherUCLen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherNuffield Department of Clinical Medicineen_US
dc.date.accessioned2019-08-23T11:17:01Z
dc.date.available2019-08-23T11:17:01Z
dc.date.issued2018-11-01en_US
dc.description.abstract© 2018 The Author(s). Background: The detection of submicroscopic infections in low prevalence settings has become an increasingly important challenge for malaria elimination strategies. The current field rapid diagnostic tests (RDTs) for Plasmodium falciparum malaria are inadequate to detect low-density infections. Therefore, there is a need to develop more sensitive field diagnostic tools. In parallel, a highly sensitive laboratory reference assay will be essential to evaluate new diagnostic tools. Recently, the highly sensitive Alere™ Malaria Ag P.f ELISA (HS ELISA) was developed to detect P. falciparum histidine-rich protein 2 (HRP2) in clinical whole blood specimens. In this study, the analytical and clinical performance of the HS ELISA was determined using recombinant P. falciparum HRP2, P. falciparum native culture parasites, and archived highly pedigreed clinical whole blood specimens from Karen village, Myanmar and Nagongera, Uganda. Results: The HS ELISA has an analytical sensitivity of less than 25 pg/mL and shows strong specificity for P. falciparum HRP2 when tested against P. falciparum native culture strains with pfhrp2 and pfhrp3 gene deletions. Additionally, the Z′-factor statistic of 0.862 indicates the HS ELISA as an excellent, reproducible assay, and the coefficients of variation for inter- and intra-plate testing, 11.76% and 2.51%, were acceptable. Against clinical whole blood specimens with concordant microscopic and PCR results, the HS ELISA showed 100% (95% CI 96.4-100) diagnostic sensitivity and 97.9% (95% CI 94.8-99.4) diagnostic specificity. For P. falciparum positive specimens with HRP2 concentrations below 400 pg/mL, the sensitivity and specificity were 100% (95% CI 88.4-100) and 88.9% (95% CI 70.8-97.6), respectively. The overall sensitivity and specificity for all 352 samples were 100% (CI 95% 96-100%) and 97.3% (CI 95% 94-99%). Conclusions: The HS ELISA is a robust and reproducible assay. The findings suggest that the HS ELISA may be a useful tool as an affordable reference assay for new ultra-sensitive HRP2-based RDTs.en_US
dc.identifier.citationMalaria Journal. Vol.17, No.1 (2018)en_US
dc.identifier.doi10.1186/s12936-018-2545-5en_US
dc.identifier.issn14752875en_US
dc.identifier.other2-s2.0-85055907719en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/45952
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85055907719&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleA new highly sensitive enzyme-linked immunosorbent assay for the detection of Plasmodium falciparum histidine-rich protein 2 in whole blooden_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85055907719&origin=inwarden_US

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