Evidence map›Paper›PMID 41354964›Full record

ArticleParasites & vectors2025

Evaluation of four chimeric Trypanosoma cruzi recombinant antigens for serological diagnosis of chronic Chagas disease in dogs: a phase II study.

Natália Dantas Fontes, Fernanda Lopes Habib, Leonardo Maia Leony, Natalia Erdens Maron Freitas, Ângelo Antônio Oliveira Silva, Filipe Dantas-Torres, Kamila Gaudêncio da Silva Sales, Andréa Pereira da Costa, Thaliane França Costa, Nayara Mendes Louzeiro and 11 more

Abstract read
In one paragraph

Article in Parasites & vectors, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. Double-antigen sandwich ELISA based on chimeric antigens for detection of antibodies to Trypanosoma cruzi in human sera - A phase II study.European journal of clinical microbiology & infectious diseases : official publication of the European Society of Clinical Microbiology · 2026
    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

21 authors.

Natália Dantas FontesAdvanced Public Health Laboratory, Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Brazil.
Fernanda Lopes HabibAdvanced Public Health Laboratory, Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Brazil.
Leonardo Maia LeonyAdvanced Public Health Laboratory, Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Brazil.
Natalia Erdens Maron FreitasAdvanced Public Health Laboratory, Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Brazil.
Ângelo Antônio Oliveira SilvaAdvanced Public Health Laboratory, Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Brazil.
Filipe Dantas-TorresLaboratory of Immunoparasitology, Department of Immunology, Aggeu Magalhães Institute, Oswaldo Cruz Foundation, Recife, Brazil.
Kamila Gaudêncio da Silva SalesLaboratory of Immunoparasitology, Department of Immunology, Aggeu Magalhães Institute, Oswaldo Cruz Foundation, Recife, Brazil.
Andréa Pereira da CostaPostgraduate Program in Animal Science, State University of Maranhão, São Luís, Brazil.
Thaliane França CostaPostgraduate Program in Animal Science, State University of Maranhão, São Luís, Brazil.
Nayara Mendes LouzeiroPostgraduate Program in Animal Science, State University of Maranhão, São Luís, Brazil.
Sidilene Pereira CostaPostgraduate Program in Animal Science, State University of Maranhão, São Luís, Brazil.
Lileia Gonçalves DiotaiutiTriatomines and Epidemiology of Chagas Disease, René Rachou Institute, Oswaldo Cruz Foundation, Belo Horizonte, Brazil.
Carlota Josefovcz BelisarioTriatomines and Epidemiology of Chagas Disease, René Rachou Institute, Oswaldo Cruz Foundation, Belo Horizonte, Brazil.
Cláudia Moura de MeloPostgraduate Program in Health and Environment, Tiradentes University, Aracaju, Brazil.
Antônia Cláudia Jácome da CâmaraDepartment of Clinical and Toxicological Analysis, Health Sciences Center, Federal University of Rio Grande Do Norte, Natal, Brazil.
Vicente Toscano de Araújo-NetoPostgraduate Program in Pharmaceutical Sciences, Federal University of Rio Grande Do Norte, Natal, Brazil.
Luanna Soares de Melo EvangelistaDepartment of Parasitology and Microbiology, Health Sciences Center, Federal University of Piauí, Teresina, Brazil.
Deborah Bittencourt MothéLaboratory of Parasite-Host Interaction and Epidemiology, Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Brazil.
Paola Alejandra Fiorani CeledonInterdisciplinary Research Group in Biotechnology and Epidemiology of Infectious Diseases (GRUPIBE), Gonçalo Moniz Institute, Oswaldo Cruz Foundation (FIOCRUZ-BA), Salvador, Brazil.
Nilson Ivo Tonin ZanchinInterdisciplinary Research Group in Biotechnology and Epidemiology of Infectious Diseases (GRUPIBE), Gonçalo Moniz Institute, Oswaldo Cruz Foundation (FIOCRUZ-BA), Salvador, Brazil.
Fred Luciano Neves SantosAdvanced Public Health Laboratory, Gonçalo Moniz Institute, Oswaldo Cruz Foundation, Salvador, Brazil. fred.santos@fiocruz.br.

Funding

Coordination of Superior Level Staff Improvement-Brazil (CAPES) 88887.509223/2020-00Coordination of Superior Level Staff Improvement-Brazil (CAPES) 88887.637758/2021-00Coordination of Superior Level Staff Improvement-Brazil (CAPES) Finance Code 001Foundation for Research Support, Scientific and Technological Development of Maranhão (FAPEMA) 001186-2019Foundation for Support to Research and Technological Innovation of the State of Sergipe (FAPITEC) 88881.157704/2017-01-PROMOBInova Fiocruz/VPPCB VPPCB-008-FIO-18-2-20National Council for Scientific and Technological Development (CNPq) 304894/2023-0National Council for Scientific and Technological Development (CNPq) 306448/2023-8National Council for Scientific and Technological Development (CNPq) 420574/2018-2National Council for Scientific and Technological Development (CNPq) 423966/2016-2National Council for Scientific and Technological Development (CNPq) 476352/2008-8Research Support Foundation of the State of Bahia (FAPESB) BOL0298/2020Research Support Foundation of the State of Bahia (FAPESB) BOL0543/2020
6 · The paper itself

Abstract

backgroundDogs are recognized as epidemiologically significant reservoirs for Trypanosoma cruzi, the causative agent of Chagas disease (CD), owing to their close association with humans and their role in sustaining the domestic and peridomestic transmission cycle. Canine seropositivity often correlates with human CD prevalence. However, the lack of commercial, high-performance diagnostic assays for canine infections remains a significant barrier to effective surveillance. Previously, our group demonstrated the diagnostic potential of four chimeric T. cruzi antigens in a phase I study, yielding results comparable to those observed in humans. The present phase II study expands upon these findings by evaluating these antigens in a larger canine cohort using indirect enzyme-linked immunosorbent assay (ELISA). The objective of this study was to assess the diagnostic performance of four chimeric recombinant T. cruzi antigens (IBMP-8.1, IBMP-8.2, IBMP-8.3, and IBMP-8.4) in immunoassays for the detection of anti-T. cruzi IgG in dogs with chronic Chagas disease.

methodsImmunoassays were optimized by checkerboard titration. In this phase II study, the diagnostic performance of the IBMP antigens was evaluated using 1260 canine serum samples. Cross-reactivity was assessed in an additional 752 samples from dogs with unrelated infectious diseases. The performance of the chimeric antigens was compared with a commercial human-adapted assay (Gold ELISA Chagas).

resultsThe Instituto de Biologia Molecular do Paraná (IBMP) antigens demonstrated area under the curve (AUC) values ranging from 89.0% to 97.4%, with diagnostic accuracy between 87.4% and 96%. IBMP-8.2 exhibited the highest sensitivity (90.3%), while IBMP-8.1, IBMP-8.3, and IBMP-8.4 achieved sensitivities of 74.8%, 72.6%, and 79.6%, respectively. The highest specificity was observed for IBMP-8.4 (99.6%), followed by IBMP-8.3 (99.0%), IBMP-8.2 (96.5%), and IBMP-8.1 (90.6%). The Gold ELISA Chagas assay showed a sensitivity of 62.3%, specificity of 98.6%, and accuracy of 89.9%. IBMP-8.2 exhibited the lowest cross-reactivity index (0.9%), closely approximating an ideal diagnostic assay.

conclusionsThe IBMP chimeric antigens demonstrated strong diagnostic performance for detecting T. cruzi infection in dogs, significantly enhancing immunoassay accuracy and minimizing diagnostic failures due to cross-reactivity. The combined use of these antigens represents a promising strategy to further improve sensitivity and specificity in future diagnostic applications.

Indexed as

Antigens, ProtozoanChagas DiseaseDog DiseasesSerologic TestsTrypanosoma cruziAnimalsAntibodies, ProtozoanChronic DiseaseDogsEnzyme-Linked Immunosorbent AssayImmunoglobulin GRecombinant ProteinsSensitivity and SpecificityAntibodies, ProtozoanAntigens, ProtozoanImmunoglobulin GRecombinant ProteinsAnthropozoonosisCanine trypanosomiasisChagas diseaseDogsImmunodiagnosticsRecombinant chimeric antigensTrypanosoma cruzi

Identifiers

PMID41354964
PMCPMC12797350

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LicenceCC BY
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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.