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Chronic immune barrier dysregulation among women with a history of violence victimization
Alison Swaims-Kohlmeier, Lisa B. Haddad, Zheng-Rong Tiger Li, Kathryn A. Brookmeyer, James M. Baker, Cathy Spatz Widom, James C. Lamousin, Kai-Hua Chi, Cheng Y. Chen, Ellen N. Kersh, Jeffrey A. Johnson, Melissa M. Herbst-Kralovetz, Matthew Hogben, Igho Ofotokun, Jacob E. Kohlmeier
Alison Swaims-Kohlmeier, Lisa B. Haddad, Zheng-Rong Tiger Li, Kathryn A. Brookmeyer, James M. Baker, Cathy Spatz Widom, James C. Lamousin, Kai-Hua Chi, Cheng Y. Chen, Ellen N. Kersh, Jeffrey A. Johnson, Melissa M. Herbst-Kralovetz, Matthew Hogben, Igho Ofotokun, Jacob E. Kohlmeier
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Research Article Immunology

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

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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.

Authors

Alison Swaims-Kohlmeier, Lisa B. Haddad, Zheng-Rong Tiger Li, Kathryn A. Brookmeyer, James M. Baker, Cathy Spatz Widom, James C. Lamousin, Kai-Hua Chi, Cheng Y. Chen, Ellen N. Kersh, Jeffrey A. Johnson, Melissa M. Herbst-Kralovetz, Matthew Hogben, Igho Ofotokun, Jacob E. Kohlmeier

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Figure 4

Stage of the menstrual cycle does not alter the impact of LTVH score on the dysregulation of memory T subsets in the FRT.

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Stage of the menstrual cycle does not alter the impact of LTVH score on ...
(A) CCR7, CD69, and CD103 expression frequency of CD4+ and CD8+ T cells from high- and low-scoring samples compared based on collections taken at the relative luteal or follicular phase of the menstrual cycle (samples depicted as box and whiskers, with box depicting the interquartile range with median bar and whiskers depicting minimum and maximum values; n = 54). Statistics calculated from longitudinal comparisons were analyzed using an unpaired 2-tailed Student’s t test, while samples compared based on high- or low-scoring LTVH were analyzed using an unpaired, 2-tailed Student’s t test. (B) Boolean analysis of CCR7, CD69, and CD103 coexpression frequency from CD4+ and CD8+ T cells measured from vaginal lavage collections taken at the relative luteal or follicular phase of the menstrual cycle and compared by low or high LTVH scores. *P < 0.05; **P < 0.01; ***P < 0.001; ****P < 0.0001. Asterisks represent a significant increase in CCR7+CD69–CD103– T cell populations (shown as red shading) in high-scoring compared with low-scoring groups at indicated phases of the menstrual cycle.

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