Evidence map›Paper›PMID 30444866›Full record

ArticlePLoS neglected tropical diseases2018

Identification and characterization of Loa loa antigens responsible for cross-reactivity with rapid diagnostic tests for lymphatic filariasis.

Marla I Hertz, Hugues Nana-Djeunga, Joseph Kamgno, Abdel Jelil Njouendou, Valerine Chawa Chunda, Samuel Wanji, Amy Rush, Peter U Fischer, Gary J Weil, Philip J Budge

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04410406 (A Clinical Trial to Assess the Safety and Efficacy of Moxidectin Combination Treatments vs. Ivermectin Combination Treatments for Bancroftian Filariasis), which is not on this map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04410406 phase3completednot on this mapstarted 2020, after this paper: background citation

A Clinical Trial to Assess the Safety and Efficacy of Moxidectin Combination Treatments vs. Ivermectin Combination Treatments for Bancroftian Filariasis

TypeinterventionalSponsorWashington University School of MedicineRan2020 to 2024Enrolled164ConditionsLymphatic FilariasisArmsIvermectin, Diethylcarbamazine, Albendazole, Moxidectin
3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  3. Review
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  5. Article
  6. Article
  7. Article
  8. Article
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  12. Article
  13. Potential use of antibodies to provide an earlier indication of lymphatic filariasis resurgence in post-mass drug ad ministration surveillance in American Samoa.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2022
    Article
  14. The Human FilariaResearch and reports in tropical medicine · 2022
    Review
  15. Article
  16. Advances in preclinical platforms ofFrontiers in tropical diseases · 2021
    Article
  17. Review
  18. Frontiers in tropical diseases · 2021
    Article
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 3 institutions in 2 countries.

Marla I HertzInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America.ORCID 0000-0001-7929-7756
Hugues Nana-DjeungaCentre for Research on Filariasis and other Tropical Diseases, Yaoundé, Cameroon.
Joseph KamgnoCentre for Research on Filariasis and other Tropical Diseases, Yaoundé, Cameroon.
Abdel Jelil NjouendouParasites and Vector Biology Research Unit (PAVBRU), Department of Microbiology and Parasitology, University of Buea, Buea, Cameroon.
Valerine Chawa ChundaParasites and Vector Biology Research Unit (PAVBRU), Department of Microbiology and Parasitology, University of Buea, Buea, Cameroon.
Samuel WanjiParasites and Vector Biology Research Unit (PAVBRU), Department of Microbiology and Parasitology, University of Buea, Buea, Cameroon.
Amy RushInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Peter U FischerInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Gary J WeilInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America.
Philip J BudgeInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St. Louis, Missouri, United States of America.ORCID 0000-0002-0069-2372
Washington University in St. Louis · USUniversity of Buea · CMUniversité de Yaoundé I · CM

Funding

TrainingP41GM103422 · NIGMS · WASHINGTON UNIVERSITY · PI GROSS, MICHAEL L · 2012 to 2019
$12.0M
IMPROVED ANTIGEN DETECTION TESTS FOR FILARIAL INFECTIONSK08AI121422 · NIAID · WASHINGTON UNIVERSITY · PI BUDGE, PHILIP · 2016 to 2020
$856k
NIAID NIH HHS K08 AI121422NIAID NIH HHS L30 AI113845NIGMS NIH HHS P41 GM103422
6 · The paper itself

Abstract

The Global Program to Eliminate Lymphatic Filariasis (LF) relies on rapid diagnostic tests (RDTs) to determine where annual mass drug administration for LF is required and when it can be stopped. These tests detect a Wuchereria bancrofti glycoprotein in the blood of infected persons via a carbohydrate moiety recognized by the monoclonal antibodies AD12 and DH6.5. Loiasis cross-reactivity with LF RDTs has recently been recognized as a serious obstacle to LF elimination in loiasis-endemic areas. To better understand the nature of this cross-reactivity, we used the DH6.5 antibody to immunoaffinity purify Loa loa antigens from the sera of individuals with a positive RDT due to loiasis. Immunoblot analysis revealed many circulating AD12/DH6.5-reactive antigens, and proteomic analysis identified multiple L. loa proteins in LF RDT-positive loiasis sera. These included both secreted and somatic proteins, suggesting that they may be released by dying L. loa adult worms and/or microfilariae. Unlike the single high molecular weight W. bancrofti circulating filarial antigen that is reliably present in the blood of persons with bancroftian filariasis, reactive L. loa antigens appeared to be only transiently present in the blood of a subset of persons with loiasis. These key differences between the circulating antigens of W. bancrofti and L. loa can be used to differentiate positive results generated by both species and may lead to improved diagnostic tests for LF and loiasis.

Indexed as

AnimalsAntibodies, HelminthAntigens, HelminthCross ReactionsDiagnostic Tests, RoutineElephantiasis, FilarialFemaleHelminth ProteinsHumansLoaWuchereria bancroftiAntibodies, HelminthAntigens, HelminthHelminth Proteins

Identifiers

PMID30444866
PMCPMC6267963
OpenAlexW2900756548

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.