Evidence map›Paper›PMID 39226306›Full record

ArticlePLoS neglected tropical diseases2024

A novel antigen biomarker for detection of high-level of Loa loa microfilaremia.

Sarah E Greene, Yuefang Huang, Kerstin Fischer, Bruce A Rosa, John Martin, Makedonka Mitreva, Devyn Yates, Samuel Wanji, Joseph Kamgno, Philip J Budge and 2 more

Abstract read
In one paragraph

Article in PLoS neglected tropical diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. 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

12 authors.

Sarah E GreeneInfectious Diseases Division, Department of Pediatrics, Washington University School of Medicine, St Louis, Missouri, United States of America.ORCID 0000-0001-6561-2698
Yuefang HuangInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, United States of America.
Kerstin FischerInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, United States of America.
Bruce A RosaInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, United States of America.
John MartinInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, United States of America.
Makedonka MitrevaInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, United States of America.
Devyn YatesInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, United States of America.
Samuel WanjiParasites and Vector Biology research unit (PAVBRU), Department of Microbiology and Parasitology, University of Buea, Buea, Cameroon.
Joseph KamgnoHigher Institute for Scientific and Medical Research (ISM), Yaoundé, Cameroon.
Philip J BudgeInfectious 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.
Peter U FischerInfectious Diseases Division, Department of Medicine, Washington University School of Medicine, St Louis, Missouri, United States of America.

Funding

Bill and Melinda Gates Foundation INV-021433Foundation for Barnes- Jewish Hospital 4930 (FBJC 5981)
6 · The paper itself

Abstract

backgroundLoiasis is a disease caused by the nematode Loa loa. Serious adverse events sometimes occur in people with heavy L. loa microfilaremia after ivermectin treatment. In regions of Central Africa where loiasis is endemic, this significantly impedes global elimination programs for lymphatic filariasis and onchocerciasis that use mass distribution of ivermectin. Improved diagnostic tests to identify individuals at increased risk of serious adverse events could facilitate efforts to eliminate lymphatic filariasis and onchocerciasis in this region. METHODS AND

findingsWe previously identified the L. loa protein Ll-Bhp-1 in loiasis patient sera. Here, we further characterize Ll-Bhp-1 and report development of an antigen capture ELISA to detect this antigen. This assay detected Ll-Bhp-1 in 74 of 116 (63.8%) loiasis patient sera. Ll-Bhp-1 levels were significantly correlated with L. loa microfilarial counts, and the sensitivity of the assay was highest for samples from people with high counts, (94% and 100% in people with ≥20,000 and ≥50,000 microfilaria per milliliter of blood, respectively). The antigen was not detected in 112 sera from people with other filarial infections, or in 34 control sera from the USA.

conclusionsThis Ll-Bhp-1 antigen assay is specific for loiasis, and highly sensitive for identifying people with high L. loa microfilarial counts who are at increased risk for serious adverse events after ivermectin treatment. L. loa antigen detection has the potential to facilitate loiasis mapping efforts and programs to eliminate lymphatic filariasis and onchocerciasis in Central Africa.

Indexed as

Antigens, HelminthBiomarkersEnzyme-Linked Immunosorbent AssayLoaLoiasisAfrica, CentralAnimalsFemaleHumansIvermectinMaleMicrofilariaeSensitivity and SpecificityAntigens, HelminthBiomarkersIvermectin

Identifiers

PMID39226306
PMCPMC11398663

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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.