Vaginal immune activity increases after first-time intercourse

Vaginal immune activity increases after first-time intercourse
Concentration of immune mediators in cervicovaginal lavage samples relative to day of first sex. Each symbol depicts the concentration in a single sample. Black lines show the slopes from mixed-effect models with days since first sex as fixed effect and participant as random effects with linear splines using a knot at day 0. Concentrations are shown in pg/mL on a log10 scale. The sample size is 80 pre-first sex samples from 59 participants and 60 post-first sex samples from 49 participants. Credit: eLife (2022). DOI: 10.7554/eLife.78565

The immune system ramps up in the vagina after young women begin having intercourse, suggests an observational study published today in eLife.

The changes detected may have important implications for sexually transmitted infection (STI) risk. But the authors do not yet know if the changes increase or decrease the risk of acquiring an STI.

Girls and between the ages of 15 and 24 have a higher risk of acquiring an STI than . However, it has not been determined if riskier behavioral choices or physiological factors may explain the increased risk.

"We measured immune changes in young women before and after initiating sex to determine if immune changes may play a role in increased STI vulnerability," says lead author Sean Hughes, a research scientist in the Department of Obstetrics and Gynecology at the University of Washington School of Medicine in Seattle, US.

Hughes and colleagues compared vaginal samples collected from 95 adolescent women in Kenya before or after they began having . They found a sharp increase in proteins that control the , including IL-1β, IL-2, and CXCL8, during the first year after the participants became sexually active. These changes were confirmed to not be due to pregnancy or having an STI.

The team reviewed data collected in two other studies to verify the result. One included 93 young women in Belgium, and another included 19 participants in the US. The combined data from those two studies also showed elevated levels of immune-controlling proteins, including IL-1β, IL-2, and CXCL8, after participants became sexually active.

"The initiation of sexual activity was associated with higher levels of immune mediators, but we don't know for sure if the start of sexual activity caused the changes," says co-senior Florian Hladik, professor in the Vaccine and Infectious Disease Division at Fred Hutchinson Cancer Center, Seattle, Washington. "Other factors associated with the timing of sex initiation, such as , could have contributed to immune system changes."

The consequences of this immune activation are also not clear. The immune changes detected in the study may help boost fertility or may be a protective defense against sexually transmitted infections. If it is an attempt at defense, it may inadvertently increase young women's vulnerability to HIV infection by recruiting the CD4 T immune cells targeted by the virus to the vagina.

More studies are needed to confirm the connection between the start of sexual activity and these immune changes and understand their consequences for young women's sexual health.

"More research on the immune changes associated with the initiation of sexual activity may help us understand the elevated STI risk in young women," says co-senior author Alison Roxby, Associate Professor of Infectious Disease and Global Health at the University of Washington School of Medicine. "It may also help us identify new ways to prevent STIs in this vulnerable population."

More information: Sean M Hughes et al, Starting to have sexual intercourse is associated with increases in cervicovaginal immune mediators in young women: a prospective study and meta-analysis, eLife (2022). DOI: 10.7554/eLife.78565

Journal information: eLife

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Citation: Vaginal immune activity increases after first-time intercourse (2022, October 25) retrieved 27 January 2023 from https://medicalxpress.com/news/2022-10-vaginal-immune-first-time-intercourse.html
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