Evidence map›Paper›PMID 41843302›Full record

ArticleActa parasitologica2026

Estudo Abrangente do Resveratrol Associado à Sulfadiazina em Linfócitos Infectados com Toxoplasma gondii: Envolvimento da Sinalização Purinérgica na Resposta Imunológica.

Nathieli Bianchin Bottari, Priscila Marquezan Copetti, Bianca Fagan Bissacotti, Taís Vidal, Anielen Dutra Da Silva, Mateus Fracasso, Karine Paula Reichert, Jelson Nauderer, Vera Maria Melchiors Morsch, Cinthia Melazzo and 2 more

Erratum issuedAbstract read
In one paragraph

Article in Acta parasitologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Nathieli Bianchin BottariDepartment of Biochemistry and Molecular Biology, Federal University of Santa Maria (UFSM), Avenida Roraima, nº1000, Camobi District, Santa Maria, RS, 97105900, Brazil. nathieli_bb@hotmail.com.
Priscila Marquezan CopettiDepartment of Biochemistry and Molecular Biology, Federal University of Santa Maria (UFSM), Avenida Roraima, nº1000, Camobi District, Santa Maria, RS, 97105900, Brazil.
Bianca Fagan BissacottiDepartment of Biochemistry and Molecular Biology, Federal University of Santa Maria (UFSM), Avenida Roraima, nº1000, Camobi District, Santa Maria, RS, 97105900, Brazil.
Taís VidalDepartment of Biochemistry and Molecular Biology, Federal University of Santa Maria (UFSM), Avenida Roraima, nº1000, Camobi District, Santa Maria, RS, 97105900, Brazil.
Anielen Dutra Da SilvaDepartment of Biochemistry and Molecular Biology, Federal University of Santa Maria (UFSM), Avenida Roraima, nº1000, Camobi District, Santa Maria, RS, 97105900, Brazil.
Mateus FracassoDepartment of Biochemistry and Molecular Biology, Federal University of Santa Maria (UFSM), Avenida Roraima, nº1000, Camobi District, Santa Maria, RS, 97105900, Brazil.
Karine Paula ReichertDepartment of Biochemistry and Molecular Biology, Federal University of Santa Maria (UFSM), Avenida Roraima, nº1000, Camobi District, Santa Maria, RS, 97105900, Brazil.
Jelson NaudererDepartment of Biochemistry and Molecular Biology, Federal University of Santa Maria (UFSM), Avenida Roraima, nº1000, Camobi District, Santa Maria, RS, 97105900, Brazil.
Vera Maria Melchiors MorschDepartment of Biochemistry and Molecular Biology, Federal University of Santa Maria (UFSM), Avenida Roraima, nº1000, Camobi District, Santa Maria, RS, 97105900, Brazil.
Cinthia MelazzoDepartment of Biochemistry and Molecular Biology, Federal University of Santa Maria (UFSM), Avenida Roraima, nº1000, Camobi District, Santa Maria, RS, 97105900, Brazil.
Aleksandro Schafer Da SilvaDepartment of Biochemistry and Molecular Biology, Federal University of Santa Maria (UFSM), Avenida Roraima, nº1000, Camobi District, Santa Maria, RS, 97105900, Brazil.
Maria Rosa Chitolina SchetingerDepartment of Biochemistry and Molecular Biology, Federal University of Santa Maria (UFSM), Avenida Roraima, nº1000, Camobi District, Santa Maria, RS, 97105900, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toxoplasma gondii is a highly successful intracellular pathogen. Its success is largely achieved by the parasite's ability to avoid the host immune response. During T. gondii infection lymphocytes play an active role in host defense and purinergic signaling has been shown to contribute to parasite control. Several studies have demonstrated the importance of ATP (adenosine triphosphate) signaling via purinergic receptor, as a component of the inflammatory response against T. gondii. Here, we hypothesized whether RSV, a natural polyphenol, could be involved in T. gondii control triggered by purinergic signaling, during acute infection in lymphocytes. Thus, the outcomes of this study were lymphocyte viability, modulation of ectonucleotidase activity, purinergic receptor expression and inflammatory mediators. T. gondii infection diminished lymphocytes viability 24h after RH-tachyzoites exposition. RSV treatment promote an increment of ATP, ADP hydrolysis by NTPDase (CD39) and adenosine deamination by ADA enzyme in infected lymphocytes. In addition, RSV upregulated P1 and P2 receptors in T. gondii-infected lymphocytes. There is an involvement of P2X

Indexed as

LymphocytesReceptors, PurinergicResveratrolSignal TransductionSulfadiazineToxoplasmaAdenosine TriphosphateAnimalsAntigens, CDApyraseCell SurvivalCytokinesHumansToxoplasmosisAdenosine TriphosphateAntigens, CDApyraseCD39 antigenCytokinesReceptors, PurinergicResveratrolSulfadiazineAdenosine receptorsCytokinesP2X7 receptorResveratrolT. gondii

Identifiers

PMID41843302
PMCPMC12995952

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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.