Evidence map›Paper›PMID 30840797›Full record

ArticleThe Korean journal of parasitology2019

Immune Response of BALB/c Mice toward Putative Calcium Transporter Recombinant Protein of Trichomonas vaginalis.

Tahali Mendoza-Oliveros, Victor Arana-Argáez, Leidi C Alvaréz-Sánchez, Julio Lara-Riegos, María Elizbeth Alvaréz-Sánchez, Julio C Torres-Romero

Open access · diamondAbstract read
In one paragraph

Article in The Korean journal of parasitology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Infinity war:Microbial cell (Graz, Austria) · 2023
    Review
  3. Clinical Manifestation and Epidemiological Finding ofIranian journal of public health · 2022
    Review
  4. 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

6 authors at 2 institutions in 1 country.

Tahali Mendoza-OliverosLaboratorio de Bioquímica y Genética Molecular, Facultad de Química de la Universidad Autónoma de Yucatán, Mérida 97069, México.
Victor Arana-ArgáezLaboratorio de Farmacología, Facultad de Química de la Universidad Autónoma de Yucatán, Mérida 97069, México.
Leidi C Alvaréz-SánchezLaboratorio de Virología, Centro de Investigaciones Regionales "Dr. Hideyo Noguchi" de la Universidad Autónoma de Yucatán, Mérida 97069, México.
Julio Lara-RiegosLaboratorio de Bioquímica y Genética Molecular, Facultad de Química de la Universidad Autónoma de Yucatán, Mérida 97069, México.
María Elizbeth Alvaréz-SánchezPosgrado en Ciencias Genómicas, Universidad Autónoma de la Ciudad de México (UACM), Ciudad de México 03100, México.
Julio C Torres-RomeroLaboratorio de Bioquímica y Genética Molecular, Facultad de Química de la Universidad Autónoma de Yucatán, Mérida 97069, México.
Autonomous University of Yucatán · MXUniversidad Autónoma de la Ciudad de México · MX

Funding

Consejo Nacional de Ciencia y Tecnología 237990
6 · The paper itself

Abstract

Trichomoniasis is a common sexually transmitted infection caused by Trichomonas vaginalis, which actually does not exist a vaccine for control or prevention. Thus, the identification of new and potent immunogens in T. vaginalis, which can contribute to the development of a vaccine against this parasite, is necessary. Therefore, the aim of this work was to evaluate the potential of a recombinant Transient Receptor Potential-like channel of T. vaginalis (TvTRPV), as a promising immunogen in BALB/c mice. First, TvTRPV was cloned and expressed as a recombinant protein in Escherichia coli BL21 cells and purified by nickel affinity. Next, BALB/c mice were immunized and the antibody levels in mice serum and cytokines from the supernatant of macrophages and from co-culture systems were evaluated. Recombinant TvTRPV triggered high levels of specific total IgG in sera from the immunized mice. Also, a statistically significant increase of cytokines: IL-1β, IL-6, and TNF-α after stimulation with the corresponding antigens in vitro, was identified. Moreover, co-cultures using CD4+ T cells from immunized mice were able to identify higher levels of IL-10 and IFN-γ. These results were useful to validate the immunogenicity of TvTRPV in BALB/c mice, where IL-10-IFN-γ-secreting cells could play a role in infection control, supporting the potential of TvTRPV as a promising target for vaccine against T. vaginalis.

Indexed as

AnimalsAntibodies, ProtozoanAntigens, ProtozoanCytokinesEscherichia coliFemaleGene ExpressionImmunoglobulin GMacrophagesMice, Inbred BALB CProtozoan VaccinesRecombinant ProteinsTrichomonas InfectionsTrichomonas vaginalisTRPV Cation ChannelsVaccines, SyntheticAntibodies, ProtozoanAntigens, ProtozoanCytokinesImmunoglobulin GProtozoan VaccinesRecombinant ProteinsTRPV Cation ChannelsVaccines, SyntheticBALB/c mouseimmune responserecombinant proteinTrichomonas vaginalisTRPV channel

Identifiers

PMID30840797
PMCPMC6409216
OpenAlexW2916387832

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.