Publication

Chronic immune barrier dysregulation among women with a history of violence victimization

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Last modified
  • 05/14/2025
Type of Material
Authors
    Alison Swaims-Kohlmeier, Centers for Disease Control and PreventionLisa Haddad, Emory UniversityZgeng-Rong Tiger Li, Emory UniversityKathryn A. Brookmeyer, Centers for Disease Control and PreventionJames M. Baker, University of ArizonaCathy Spatz Widom, City University of New YorkJames C. Lamousin, South Mississippi State HospitalKai-Hua Chi, Centers for Disease Control and PreventionChen Y. Chen, Centers for Disease Control and PreventionEllen N. Kersh, Centers for Disease Control and PreventionJeffery A. Johnson, Centers for Disease Control and PreventionMelissa M. Herbst-Kralovetz, University of ArizonaMatthew Hogben, Centers for Disease Control and PreventionIghovwerha Ofotokun, Emory UniversityJacob Kohlmeier, Emory University
Language
  • English
Date
  • 2019-05-16
Publisher
  • American Society for Clinical Investigation
Publication Version
Copyright Statement
  • © 2019 American Society for Clinical Investigation
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 2379-3708
Volume
  • 4
Issue
  • 10
Grant/Funding Information
  • This study was supported by the US CDC and Emory University and in part by NIH grants R01HL122559 (to JEK); 1R15AI113457-01A1 (to MMHK); and K23HD078153-01A1 (to LBH); the Emory University Center for AIDS research (P30AI050409); and the Atlanta Clinical and Translational Sciences Institute (KLR2TR000455, UL1TR000454).
Supplemental Material (URL)
Abstract
  • We explored the association between violence victimization and increased risk for acquiring sexually transmitted infections (STIs) in women by measuring cellular immune barrier properties from the female reproductive tract. STI-negative participants reporting repeated prior victimization occurrences through the lifetime trauma and victimization history (LTVH) instrument were more likely to exhibit alterations in barrier homeostasis and the composition of critical immune mediators irrespective of demographic parameters or presence of bacterial vaginosis. By combining cellular data with mixed-effect linear modeling, we uncovered differences in local T cells, MHCII+ antigen-presenting cells, and epithelial cells indicative of altered trafficking behavior, increased immunosuppressive function, and decreased barrier integrity at sites of STI exposure that correlate most strongly with LTVH score. These data evidence a biological link between a history of violence victimization and risk of STI acquisition through immune dysregulation in the female reproductive tract.
Author Notes
  • Jacob E. Kohlmeier, Department of Microbiology and Immunology, Emory University School of Medicine, Atlanta, Georgia 30322, USA. Phone: 404.727.7023; Email: jkohlmeier@emory.edu.
Keywords
Research Categories
  • Health Sciences, Obstetrics and Gynecology
  • Health Sciences, Immunology
  • Health Sciences, Mental Health

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