Evidence map›Paper›PMID 38276916›Full record

ArticleImmunoHorizons2024

Antibody Response to the Sneathia vaginalis Cytopathogenic Toxin A during Pregnancy.

Zion T McCoy, Myrna G Serrano, Laahirie Edupuganti, Katherine M Spaine, David J Edwards, Gregory A Buck, Kimberly K Jefferson

Open access · goldAbstract read
In one paragraph

Article in ImmunoHorizons, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Review
  2. 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

7 authors at 1 institution in 1 country.

Zion T McCoyDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA.
Myrna G SerranoDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA.
Laahirie EdupugantiDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA.
Katherine M SpaineDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA.
David J EdwardsCenter for Microbiome Engineering and Data Analysis, Virginia Commonwealth University, Richmond, VA.
Gregory A BuckDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA.
Kimberly K JeffersonDepartment of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA.
Virginia Commonwealth University · US

Funding

A Multi-'omic Analysis of the Vaginal Microbiome during PregnancyU54HD080784 · NICHD · VIRGINIA COMMONWEALTH UNIVERSITY · PI BUCK, GREGORY ALLEN, JEFFERSON, KIMBERLY KAY · 2014 to 2015
$8.2M
"Role of the cytotoxin, CptA, from the emerging bacterial pathogen Sneathia vaginalis, in pathogenesis"R21AI166168 · NIAID · VIRGINIA COMMONWEALTH UNIVERSITY · PI JEFFERSON, KIMBERLY KAY · 2023 to 2024
$427k
NIAID NIH HHS R21 AI166168NICHD NIH HHS U54 HD080784
6 · The paper itself

Abstract

Sneathia vaginalis is a Gram-negative vaginal species that is associated with pregnancy complications. It produces cytopathogenic toxin A (CptA), a pore-forming toxin. To determine whether CptA is expressed in vivo and to examine the mucosal Ab response to the toxin, we examined human midvaginal swab samples obtained during pregnancy for IgM, IgA, and IgG Abs with CptA affinity. This subcohort study included samples from 93 pregnant people. S. vaginalis relative abundance was available through 16S rRNA survey. There were 22 samples from pregnancies that resulted in preterm birth in which S. vaginalis relative abundance was <0.005%, 22 samples from pregnancies that resulted in preterm birth with S. vaginalis ≥0.005%, 24 samples from pregnancies that resulted in term birth with S. vaginalis <0.005%, and 25 samples from pregnancies that resulted in term birth with S. vaginalis ≥0.005%. IgM, IgA, and IgG with affinity for CptA were assessed by ELISA. The capacity for the samples to neutralize CptA was quantified by hemolysis assay. All three Ab isotypes were detectable within different subsets of the samples. There was no significant association between relative abundance of S. vaginalis and the presence of any Ab isotype. The majority of vaginal swab samples containing detectable levels of anti-CptA Abs neutralized the hemolytic activity of CptA, with the strongest correlation between IgA and neutralizing activity. These results demonstrate that S. vaginalis produces CptA in vivo and that CptA is recognized by the host immune defenses, resulting in the production of Abs with toxin-neutralizing ability.

Indexed as

EthylaminesPremature BirthAntibody FormationFemaleHumansImmunoglobulin AImmunoglobulin GImmunoglobulin MInfant, NewbornPregnancyRNA, Ribosomal, 16S2-(4-chlorophenylthio)triethylamineEthylaminesImmunoglobulin AImmunoglobulin GImmunoglobulin MRNA, Ribosomal, 16S

Identifiers

PMID38276916
PMCPMC10832334
OpenAlexW4391263712

What OpenQuestion holds

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LicenceCC BY-NC
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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.