Evidence map›Paper›PMID 38386594›Full record

ArticleImmunoHorizons2024

A Noninvasive Method to Sample Immune Cells in the Lower Female Genital Tract Using Menstrual Discs.

M Quinn Peters, Eva Domenjo-Vila, Marc Carlson, Blair Armistead, Paul T Edlefsen, Melanie Gasper, Smritee Dabee, Christopher Whidbey, Heather B Jaspan, Martin Prlic and 1 more

Abstract 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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Genital Tract and Circulating CD8+ T Cell Phenotypes Vary Across the Menstrual Cycle.American journal of reproductive immunology (New York, N.Y. : 1989) · 2026
    Article
  2. T-Cell Biology in the Female Reproductive Tract: Relevance to HIV Infection.American journal of reproductive immunology (New York, N.Y. : 1989) · 2026
    Review
  3. UnveilingiScience · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors.

M Quinn PetersCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.ORCID 0000-0001-9832-3219
Eva Domenjo-VilaVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.ORCID 0000-0003-0678-4478
Marc CarlsonResearch Scientific Computing, Enterprise Analytics, Seattle Children's Research Institute, Seattle, WA.
Blair ArmisteadCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.ORCID 0000-0001-9902-3955
Paul T EdlefsenVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
Melanie GasperCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.
Smritee DabeeCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.
Christopher WhidbeyDepartment of Chemistry, Seattle University, Seattle, WA.ORCID 0000-0002-2039-4284
Heather B JaspanCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.
Martin PrlicVaccine and Infectious Disease Division, Fred Hutchinson Cancer Center, Seattle, WA.
Whitney E HarringtonCenter for Global Infectious Disease Research, Seattle Children's Research Institute, Seattle, WA.ORCID 0000-0002-0121-978X

Funding

SDMC: HIV Vaccine Trials NetworkUM1AI068635 · NIAID · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Peter B. Gilbert, Yunda Huang · 2011 to 2026
$385.9M
The regulatory role of natural progesterone in barrier immunityR01AI172111 · NIAID · UNIVERSITY OF WASHINGTON · PI Florian Hladik, Jennifer M Lund · 2022 to 2026
$4.3M
The Effect of Maternal Cells on Infant ImmunityK08AI135072 · NIAID · SEATTLE CHILDREN'S HOSPITAL · PI HARRINGTON, WHITNEY ELIZABETH · 2018 to 2022
$854k
NIAID NIH HHS K08 AI135072NIAID NIH HHS R01 AI172111NIAID NIH HHS UM1 AI068635Wellcome Trust 1017213
6 · The paper itself

Abstract

T cells in the human female genital tract (FGT) are key mediators of susceptibility to and protection from infection, including HIV and other sexually transmitted infections. There is a critical need for increased understanding of the distribution and activation of T cell populations in the FGT, but current sampling methods require a healthcare provider and are expensive, limiting the ability to study these populations longitudinally. To address these challenges, we have developed a method to sample immune cells from the FGT utilizing disposable menstrual discs which are noninvasive, self-applied, and low in cost. To demonstrate reproducibility, we sampled the cervicovaginal fluid of healthy, reproductive-aged individuals using menstrual discs across 3 sequential days. Cervicovaginal fluid was processed for cervicovaginal cells, and high-parameter flow cytometry was used to characterize immune populations. We identified large numbers of live, CD45+ leukocytes, as well as distinct populations of T cells and B cells. Within the T cell compartment, activation and suppression status of T cell subsets were consistent with previous studies of the FGT utilizing current approaches, including identification of both tissue-resident and migratory populations. In addition, the T cell population structure was highly conserved across days within individuals but divergent across individuals. Our approach to sample immune cells in the FGT with menstrual discs will decrease barriers to participation and empower longitudinal sampling in future research studies.

Indexed as

HIV InfectionsAdultFemaleGenitalia, FemaleHumansReproducibility of ResultsT-Lymphocyte Subsets

Identifiers

PMID38386594
PMCPMC10916362

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.