Evidence map›Paper›PMID 28294160›Full record

ArticleScientific reports2017

Immune complexes in chronic Chagas disease patients are formed by exovesicles from Trypanosoma cruzi carrying the conserved MASP N-terminal region.

Isabel María Díaz Lozano, Luis Miguel De Pablos, Silvia Andrea Longhi, María Paola Zago, Alejandro Gabriel Schijman, Antonio Osuna

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

37 citing papers in PubMed, 54 citations in OpenAlex.

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  17. Role of a 49 kDaPathogens (Basel, Switzerland) · 2023
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  19. Extracellular vesicles ofFrontiers in immunology · 2023
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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

6 authors at 3 institutions in 3 countries.

Isabel María Díaz LozanoDepartamento de Parasitología, Grupo de Bioquímica y Parasitología Molecular, Campus de Fuentenueva, Universidad de Granada, 18071 Granada, Spain.
Luis Miguel De PablosDepartamento de Parasitología, Grupo de Bioquímica y Parasitología Molecular, Campus de Fuentenueva, Universidad de Granada, 18071 Granada, Spain.
Silvia Andrea LonghiLabMeCh, INGEBI-CONICET, Buenos Aires, Argentina.
María Paola ZagoInstituto de Patología Experimental (IPE) CONICET-UNSa, Argentina.
Alejandro Gabriel SchijmanLabMeCh, INGEBI-CONICET, Buenos Aires, Argentina.
Antonio OsunaDepartamento de Parasitología, Grupo de Bioquímica y Parasitología Molecular, Campus de Fuentenueva, Universidad de Granada, 18071 Granada, Spain.
Consejo Nacional de Investigaciones Científicas y Técnicas · ARUniversidad de Granada · ESUniversity of York · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The exovesicles (EVs) are involved in pathologic host-parasite immune associations and have been recently used as biomarkers for diagnosis of infectious diseases. The release of EVs by Trypanosoma cruzi, the causative agent of Chagas disease, has recently been described, with different protein cargoes including the MASP multigene family of proteins MASPs are specific to this parasite and characterized by a conserved C-terminal (C-term) region and an N-terminal codifying for a signal peptide (SP). In this investigation, we identified immature MASP proteins containing the MASP SP in EVs secreted by the infective forms of the parasite. Those EVs are responsible for the formation of immune complexes (ICs) containing anti-MASP SP IgGs in patients with different (cardiac, digestive and asymptomatic) chronic Chagas disease manifestations. Moreover, purified EVs as well as the MASP SP inhibit the action of the complement system and also show a significant association with the humoral response in patients with digestive pathologies. These findings reveal a new route for the secretion of MASP proteins in T. cruzi, which uses EVs as vehicles for immature and misfolded proteins, forming circulating immune complexes. Such complexes could be used in the prognosis of digestive pathologies of clinical forms of Chagas disease.

Indexed as

AnimalsAntigen-Antibody ComplexAntigens, ProtozoanBiomarkersChagas DiseaseExtracellular VesiclesHost-Parasite InteractionsHumansMannose-Binding Protein-Associated Serine ProteasesProtein Sorting SignalsTrypanosoma cruziAntigen-Antibody ComplexAntigens, ProtozoanBiomarkersMannose-Binding Protein-Associated Serine ProteasesProtein Sorting Signals

Identifiers

PMID28294160
PMCPMC5353755
OpenAlexW2639265081

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.