Evidence map›Paper›PMID 29425201›Full record

ArticlePLoS neglected tropical diseases2018

A novel antibody surrogate biomarker to monitor parasite persistence in Trypanosoma cruzi-infected patients.

Maan Zrein, Elodie Granjon, Lucie Gueyffier, Julie Caillaudeau, Peter Liehl, Hans Pottel, Clareci Silva Cardoso, Claudia Di Lorenzo Oliveira, Lea Campos de Oliveira, Tzong-Hae Lee and 4 more

Open 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. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
5.8field-weighted citation impact, top 3% 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

22 citing papers in PubMed, 46 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Assessment of Cross-Reactivity of ChimericDiagnostics (Basel, Switzerland) · 2023
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  7. Observational
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  13. Cohort profile update: the main and new findings from the SaMi-Trop Chagas cohort.Revista do Instituto de Medicina Tropical de Sao Paulo · 2021
    Article
  14. Article
  15. Article
  16. Article
  17. TcTASV Antigens ofThe American journal of tropical medicine and hygiene · 2019
    Article
  18. Article
  19. Article
  20. Pathology and Pathogenesis of Chagas Heart Disease.Annual review of pathology · 2019
    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

14 authors at 6 institutions in 3 countries.

Maan ZreinR&D, INFYNITY BIOMARKERS SAS, Lyon, France.ORCID 0000-0002-3301-4252
Elodie GranjonR&D, INFYNITY BIOMARKERS SAS, Lyon, France.
Lucie GueyffierR&D, INFYNITY BIOMARKERS SAS, Lyon, France.
Julie CaillaudeauR&D, INFYNITY BIOMARKERS SAS, Lyon, France.
Peter LiehlR&D, INFYNITY BIOMARKERS SAS, Lyon, France.
Hans PottelFaculty of Medicine, University of Leuven (KULAK), Kortrijk, Belgium.
Clareci Silva CardosoFederal University of São João del-Rey, Research Group in Epidemiology and New Technologies in Health-campus CCO, São João del-Rei, Brazil.
Claudia Di Lorenzo OliveiraFederal University of São João del-Rey, Research Group in Epidemiology and New Technologies in Health-campus CCO, São João del-Rei, Brazil.
Lea Campos de OliveiraInstituto de Medicina Tropical e Faculdade de Medicina (FMUSP) da Universidade de São Paulo, São Paulo, Brazil.
Tzong-Hae LeeBlood Systems Research Institute and University of California, San Francisco, California, United States of America.
Ariela Mota FerreiraGraduate Program in Health Sciences, State University of Montes Claros (Universidade Estadual de Montes Claros), Montes Claros, Minas Gerais, Brazil.
Antonio Luiz P RibeiroHospital das Clínicas and School of Medicine, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Michael P BuschBlood Systems Research Institute and University of California, San Francisco, California, United States of America.
Ester Cerdeira SabinoInstituto de Medicina Tropical e Faculdade de Medicina (FMUSP) da Universidade de São Paulo, São Paulo, Brazil.
Federal University of São João del-Rei · BRHospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo · BRUniversity of California, San Francisco · USHospital das Clínicas da Universidade Federal de Minas Gerais · BRKU Leuven · BEUniversidade Estadual de Montes Claros · BR

Funding

Sao Paulo-Minas Gerais Tropical Medicine Research Center for Chagas Disease Biomarker DiscoveryU19AI098461 · NIAID · FUNDACAO FACULDADE DE MEDICINA · PI SABINO, ESTER CERDEIRA · 2017 to 2021
$2.1M
Sao Paulo- MInas Gerais Neglected Tropical Disease Research Center for BiomarkerP50AI098461 · NIAID · FUNDACAO FACULDADE DE MEDICINA · PI CUNHA-NETO, EDECIO · 2012 to 2016
$1.5M
NIAID NIH HHS P50 AI098461NIAID NIH HHS U19 AI098461
6 · The paper itself

Abstract

backgroundTrypanosoma cruzi parasite, the causative agent of Chagas disease, infects about six million individuals in more than 20 countries. Monitoring parasite persistence in infected individuals is of utmost importance to develop and evaluate treatments to control the disease. Routine screening for infected human individuals is achieved by serological assays; PCR testing to monitor spontaneous or therapy-induced parasitological cure has limitations due to the low and fluctuating parasitic load in circulating blood. The aim of the present study is to evaluate a newly developed antibody profiling assay as an indirect method to assess parasite persistence based on waning of antibodies following spontaneous or therapy-induced clearance of the infection. METHODOLOGY/PRINCIPAL

findingsWe designed a multiplex serology assay, an array of fifteen optimized T. cruzi antigens, to evaluate antibody diversity in 1654 serum samples from chronic Chagas patients. One specific antibody response (antibody 3, Ab3) showed a strong correlation with T. cruzi parasite persistence as determined by T. cruzi PCR positive results. High and sustained Ab3 signal was strongly associated with PCR positivity in untreated patients, whereas significant decline in Ab3 signals was observed in BZN-treated patients who cleared parasitemia based on blood PCR results. CONCLUSION/SIGNIFICANCE: Ab3 is a new surrogate biomarker that strongly correlates with parasite persistence in chronic and benznidazole-treated Chagas patients. We hypothesize that Ab3 is induced and maintained by incessant stimulation of the immune system by tissue-based and shed parasites that are not consistently detectable by blood based PCR techniques. Hence, a simple immunoassay measurement of Ab3 could be beneficial for monitoring the infectious status of seropositive patients.

Indexed as

AnimalsAntibodies, ProtozoanAntigens, ProtozoanBiomarkersBrazilChagas DiseaseDNA, ProtozoanHumansImmunoassayNitroimidazolesParasite LoadParasitemiaPolymerase Chain ReactionSensitivity and SpecificitySerologic TestsTrypanosoma cruziAntibodies, ProtozoanAntigens, ProtozoanbenzonidazoleBiomarkersDNA, ProtozoanNitroimidazoles

Identifiers

PMID29425201
PMCPMC5823467
OpenAlexW2785563596

What OpenQuestion holds

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Registered trials

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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.