Evidence map›Paper›PMID 32444843›Full record

ArticleScientific reports2020

The impact of cervical cytobrush sampling on cervico-vaginal immune parameters and microbiota relevant to HIV susceptibility.

A Mohammadi, S Bagherichimeh, M C Perry, A Fazel, E Tevlin, S Huibner, W Tharao, B Coburn, R Kaul

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 18 citations in OpenAlex.

  1. Trial
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  4. Review
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  12. Interactions between microbiota and cervical epithelial, immune, and mucus barrier.Frontiers in cellular and infection microbiology · 2023
    Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Mucosal Immunity and HIV Acquisition in Women.Current opinion in physiology · 2021
    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

9 authors at 2 institutions in 1 country.

A MohammadiDepartment of Medicine, University of Toronto, Toronto, Canada. Avid.mohammadi@mail.utoronto.ca.
S BagherichimehDepartment of Medicine, University of Toronto, Toronto, Canada.
M C PerryDepartment of Immunology, University of Toronto, Toronto, Canada.
A FazelDepartment of Medicine, University of Toronto, Toronto, Canada.
E TevlinWomen's Health in Women's Hands Community Health Center, Toronto, Canada.
S HuibnerDepartment of Medicine, University of Toronto, Toronto, Canada.
W TharaoWomen's Health in Women's Hands Community Health Center, Toronto, Canada.
B CoburnDepartment of Immunology, University of Toronto, Toronto, Canada.
R KaulDepartment of Medicine, University of Toronto, Toronto, Canada. Rupert.kaul@utoronto.ca.
University of Toronto · CAWomen's Health In Women's Hands · CA

Funding

CIHR
6 · The paper itself

Abstract

The immunology and microbiota of the female genital tract (FGT) are key determinants of HIV susceptibility. Cervical cytobrush sampling is a relatively non-invasive method permitting the longitudinal assessment of endocervical immune cells, but effects on FGT immunology are unknown. Blood, cervico-vaginal secretions and cervical cytobrushes were collected from sexually transmitted infection (STI)-free women at baseline and after either 6 hours or 48 hours. Endocervical immune cell subsets were assessed by flow cytometry, and pro-inflammatory cytokines by multiplex ELISA. The density of Lactobacillus species and key bacterial vaginosis-associated bacterial taxa were determined by qPCR. Paired changes were assessed before and after cytobrush sampling. After 6 hours there were significant increases in CD4 + T cell, antigen presenting cell (APC) and neutrophil numbers; APC elevations persisted at 48 hours, while neutrophil and CD4 + T cell numbers returned to baseline. In addition, pro-inflammatory cytokine levels were increased at 6 hours and returned to baseline by 48 hours. No significant changes were observed in the absolute abundance of Lactobacillus species or BV-associated bacteria at either time point. Overall, cytobrush sampling altered genital immune parameters at 6 hours, but only APC number increases persisted at 48 hours. This should be considered in longitudinal analyses of FGT immunology.

Indexed as

AdolescentAdultCanadaCervix UteriCytokinesFemaleHIVHIV InfectionsHumansMicrobiotaProspective StudiesSpecimen HandlingVaginaVaginosis, BacterialViral LoadYoung AdultCytokines

Identifiers

PMID32444843
PMCPMC7244754
OpenAlexW3026857847

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.