Evidence map›Paper›PMID 39565824›Full record

ArticlePLoS neglected tropical diseases2024

Circulating extracellular vesicles in sera of chronic patients as a method for determining active parasitism in Chagas disease.

Noelia Lozano, Alexa Prescilla-Ledezma, Eva Calabuig, Maria Trelis, José Miguel Sahuquillo Arce, José Luis López Hontangas, Luis Miguel de Pablos, Mercedes Gomez-Samblas, Antonio Osuna

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.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
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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.

Noelia LozanoArea of Parasitology, Department of Pharmacy and Pharmaceutical Technology and Parasitology, University of Valencia, Burjassot, Valencia, Spain.
Alexa Prescilla-LedezmaDepartment of Human Microbiology, Faculty of Medicine, University of Panama, Panama.
Eva CalabuigInfectious Diseases Unit, Internal Medicine Department, Hospital Universitario y Politécnico La Fe, Martorell, Valencia, Spain.
Maria TrelisArea of Parasitology, Department of Pharmacy and Pharmaceutical Technology and Parasitology, University of Valencia, Burjassot, Valencia, Spain.
José Miguel Sahuquillo ArceDepartment of Clinical Microbiology and Parasitology, Hospital Universitario y Politécnico La Fe, Martorell, Valencia, Spain.
José Luis López HontangasDepartment of Clinical Microbiology and Parasitology, Hospital Universitario y Politécnico La Fe, Martorell, Valencia, Spain.
Luis Miguel de PablosDepartment of Parasitology, Biochemical and Molecular Parasitology Group CTS-183, and Institute of Biotechnology, University of Granada., Granada, Spain.
Mercedes Gomez-SamblasDepartment of Parasitology, Biochemical and Molecular Parasitology Group CTS-183, and Institute of Biotechnology, University of Granada., Granada, Spain.
Antonio OsunaDepartment of Parasitology, Biochemical and Molecular Parasitology Group CTS-183, and Institute of Biotechnology, University of Granada., Granada, Spain.ORCID 0000-0002-3818-1471

Funding

Fundación Ramón Areces
6 · The paper itself

Abstract

backgroundChagas disease, once restricted mainly to the Americas, Chagas disease has become a global health problem due to migration from endemic to non-endemic areas. In non-endemic regions, transmission is limited to vertical transmission from infected mothers to newborns or through blood and organ donations. A major challenge in the management of the disease lies in the diagnosis of chronic cases, as blood-borne parasites are often absent and antibodies persist for life, complicating the evaluation of treatment. METHODOLOGY AND MAIN

findingsThis study investigates whether detection of circulating extracellular vesicles (EVs) or their immunocomplexes with host IgGs in the serum of chronic patients with Chagas disease could serve as diagnostic tools and biomarkers of the active presence of the parasite. This method may prove valuable in cases where parasitaemia and other diagnostic tests are inconclusive, especially for assessing treatment efficacy and confirming mother-to-child transmission. Together with exovesicle purification by ultracentrifugation, which is the 'gold standard', an affordable and simplified method for the isolation of EVs or immunocomplexes was tested for use in less well-equipped diagnostic laboratories. EV detection was performed by enzyme-linked immunosorbent assay (ELISA) targeting Trypanosoma cruzi antigens. Positive results were demonstrated in Bolivian patients in Spain, covering asymptomatic and symptomatic cases (cardiac, gastrointestinal or both). The study also examined infected mothers and their newborns. These findings were further confirmed in Panamanian patients with inconclusive diagnostic results. Moreover, host IgG isotypes that formed immunocomplexes with parasite exovsicles were identified, with IgG2 and IgG4 being predominant.

conclusionsOur results confirm the usefulness of circulating EVs and their immunocomplexes as markers of metabolically active T. cruzi in chronic infections without detectable parasitaemia, as well as their efficacy in confirming vertical transmission and in cases of inconclusive diagnostic tests.

Indexed as

Chagas DiseaseEnzyme-Linked Immunosorbent AssayExtracellular VesiclesTrypanosoma cruziAdultAntibodies, ProtozoanAntigens, ProtozoanBiomarkersBoliviaChronic DiseaseFemaleHumansImmunoglobulin GInfectious Disease Transmission, VerticalMaleMiddle AgedAntibodies, ProtozoanAntigens, ProtozoanBiomarkersImmunoglobulin G

Identifiers

PMID39565824
PMCPMC11616892

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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.