Evidence map›Paper›PMID 27007679›Full record

ArticleMucosal immunology2016

Medroxyprogesterone acetate and levonorgestrel increase genital mucosal permeability and enhance susceptibility to genital herpes simplex virus type 2 infection.

N E Quispe Calla, R D Vicetti Miguel, P N Boyaka, L Hall-Stoodley, B Kaur, W Trout, S D Pavelko, T L Cherpes

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in Mucosal immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02011711 (Modulation of Mucosal and Systemic Immunity by Hormonal Contraceptives), which is not on this map. Cited by 64 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed, 1 pooled it
8.7field-weighted citation impact, top 2% 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.

NCT02011711 completednot on this map

Modulation of Mucosal and Systemic Immunity by Hormonal Contraceptives

TypeobservationalSponsorThomas L. CherpesRan2013 to 2016Enrolled90ConditionsContraception
3 · Its place in the literature

Who cites it

64 citing papers in PubMed, 1 synthesis or guideline pooled it, 84 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Genital inflammatory status and the innate immune response to contraceptive initiation.American journal of reproductive immunology (New York, N.Y. : 1989) · 2022
    Trial
  4. Trial
  5. Trial
  6. Trial
  7. Toxicants in sexual health products: highlighting a critical research gap.Journal of exposure science & environmental epidemiology · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Frontiers in immunology · 2024
    Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

4 more citing papers are in PubMed but not listed here.

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

8 authors at 2 institutions in 1 country.

N E Quispe CallaDepartment of Microbial Infection and Immunity, Columbus, Ohio, USA.
R D Vicetti MiguelDepartment of Microbial Infection and Immunity, Columbus, Ohio, USA.
P N BoyakaDepartment of Veterinary Biosciences, The Ohio State University College of Veterinary Medicine, Columbus, Ohio, USA.
L Hall-StoodleyDepartment of Microbial Infection and Immunity, Columbus, Ohio, USA.
B KaurDepartment of Neurological Surgery, James Comprehensive Cancer Center, The Ohio State University Medical Center, Columbus, Ohio, USA.
W TroutDepartment of Obstetrics and Gynecology, The Ohio State University College of Medicine, Columbus, Ohio, USA.
S D PavelkoDepartment of Microbial Infection and Immunity, Columbus, Ohio, USA.
T L CherpesDepartment of Microbial Infection and Immunity, Columbus, Ohio, USA.
The Ohio State University · USNeurological Surgery · US

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
The Tumor Microenvironmental Barrier to Effective Viral OncolysisP01CA163205 · NCI · OHIO STATE UNIVERSITY · PI MICHAEL A CALIGIURI · 2013 to 2026
$26.0M
Enhancing Viral Oncolysis with Vasculostatin Gene DeliveryR01CA150153 · NCI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KAUR, BALVEEN · 2011 to 2020
$4.0M
OV Therapy Induced Changes in Tumor Secretome and Their Impact on TherapyR01NS064607 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KAUR, BALVEEN · 2008 to 2018
$3.2M
Modulation of Hormonal and Systemic Immunity by Hormonal Contraceptive UseR01HD072663 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TROUT, WAYNE C · 2012 to 2016
$2.1M
NCI NIH HHS P01 CA163205NCI NIH HHS P30 CA016058NCI NIH HHS R01 CA150153NICHD NIH HHS R01 HD072663NINDS NIH HHS R01 NS064607
6 · The paper itself

Abstract

Depot-medroxyprogesterone acetate (DMPA) is a hormonal contraceptive especially popular in areas with high prevalence of HIV and other sexually transmitted infections (STI). Although observational studies identify DMPA as an important STI risk factor, mechanisms underlying this connection are undefined. Levonorgestrel (LNG) is another progestin used for hormonal contraception, but its effect on STI susceptibility is much less explored. Using a mouse model of genital herpes simplex virus type 2 (HSV-2) infection, we herein found that DMPA and LNG similarly reduced genital expression of the desmosomal cadherin desmoglein-1α (DSG1α), enhanced access of inflammatory cells to genital tissue by increasing mucosal epithelial permeability, and increased susceptibility to viral infection. Additional studies with uninfected mice revealed that DMPA-mediated increases in mucosal permeability promoted tissue inflammation by facilitating endogenous vaginal microbiota invasion. Conversely, concomitant treatment of mice with DMPA and intravaginal estrogen restored mucosal barrier function and prevented HSV-2 infection. Evaluating ectocervical biopsy tissue from women before and 1 month after initiating DMPA remarkably revealed that inflammation and barrier protection were altered by treatment identically to changes seen in progestin-treated mice. Together, our work reveals DMPA and LNG diminish the genital mucosal barrier; a first-line defense against all STI, but may offer foundation for new contraceptive strategies less compromising of barrier protection.

Indexed as

Disease SusceptibilityAnimalsContraceptive Agents, FemaleDisease Models, AnimalEstrogensFemaleHerpes GenitalisHerpesvirus 2, HumanLevonorgestrelMedroxyprogesterone AcetateMiceMucous MembranePermeabilityVaginaContraceptive Agents, FemaleEstrogensLevonorgestrelMedroxyprogesterone Acetate

Identifiers

PMID27007679
PMCPMC5035233
OpenAlexW2311480849

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.