Evidence map›Paper›PMID 32324742›Full record

ArticlePLoS neglected tropical diseases2020

Urine-based antigen detection assay for diagnosis of visceral leishmaniasis using monoclonal antibodies specific for six protein biomarkers of Leishmania infantum / Leishmania donovani.

Claudia Abeijon, Fabiana Alves, Séverine Monnerat, Jane Mbui, Agostinho G Viana, Raquel M Almeida, Lilian L Bueno, Ricardo T Fujiwara, Antonio Campos-Neto

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in PLoS neglected tropical diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 15% 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.

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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Review
  7. Proteomic Analysis of Urine from Patients withTropical medicine and infectious disease · 2022
    Article
  8. Molecular Tracking of theFrontiers in cellular and infection microbiology · 2021
    Review
  9. Precision Medicine in Control of Visceral Leishmaniasis Caused byFrontiers in cellular and infection microbiology · 2021
    Review
  10. Review
  11. Review
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

9 authors at 4 institutions in 4 countries.

Claudia AbeijonDetectoGen Inc., Grafton, Massachusetts, United States of America.
Fabiana AlvesDrugs for Neglected Diseases Initiative, Geneva, Switzerland.
Séverine MonneratDrugs for Neglected Diseases Initiative, Geneva, Switzerland.
Jane MbuiKEMRI Centre for Clinical Research, Nairobi, Kenya.
Agostinho G VianaKEMRI Centre for Clinical Research, Nairobi, Kenya.
Raquel M AlmeidaFederal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Lilian L BuenoFederal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Ricardo T FujiwaraFederal University of Minas Gerais, Belo Horizonte, MG, Brazil.
Antonio Campos-NetoDetectoGen Inc., Grafton, Massachusetts, United States of America.ORCID 0000-0003-1355-2798
Universidade Federal de Minas Gerais · BRDrugs for Neglected Diseases Initiative · CHKenya Medical Research Institute · KETufts University · US

Funding

Novel non-invasive antigen detection assay for the diagnosis of active visceral leishmaniasis and to monitor the therapy efficacy of this diseaseR44AI113992 · NIAID · DETECTOGEN, INC. · PI ABEIJON, CLAUDIA · 2017 to 2019
$1.9M
NIAID NIH HHS R44 AI113992
6 · The paper itself

Abstract

The development of an accurate protein-based antigen detection assay for diagnosis of active visceral leishmaniasis (VL) would represent a major clinical advance. VL is a serious and fatal disease caused by the parasites Leishmania infantum and Leishmania donovani. The gold standard confirmatory diagnostic test for VL is the demonstration of parasites or their DNA from aspirates from spleen, lymph node, and bone marrow or from blood buffy coats. Here we describe the production and use of monoclonal antibodies (mAbs) for the development of a sensitive and specific antigen detection capture ELISA for VL diagnosis. This test simultaneously detects six leishmania protein biomarkers that we have previously described (Li-isd1, Li-txn1, Li-ntf2, Ld-mao1, Ld-ppi1 and Ld-mad1). The initial clinical validation of this new mAb-based multiplexed capture ELISA showed a sensitivity of ≥93%. The test was negative with 35 urine samples from healthy control subjects as well as with 30 patients with confirmed non-VL tropical diseases (cutaneous leishmaniasis, n = 6; Chagas disease, n = 6; schistosomiasis, n = 6; and tuberculosis, n = 12). These results strongly support the possible utility of this mAb-based multiplexed capture ELISA as a promising diagnostic test for active VL as well as for monitoring the treatment efficacy of this disease. The test is ready for upscaling and validation for clinical use.

Indexed as

AdolescentAdultAgedAntibodies, MonoclonalAntibodies, ProtozoanAntigens, ProtozoanBiomarkersChildChild, PreschoolEnzyme-Linked Immunosorbent AssayFemaleHumansLeishmania donovaniLeishmania infantumLeishmaniasis, VisceralMaleAntibodies, MonoclonalAntibodies, ProtozoanAntigens, ProtozoanBiomarkers

Identifiers

PMID32324742
PMCPMC7200010
OpenAlexW3019884051

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.