A Network Analysis of Lifetime Stressor Exposure, Mental Health, Well-Being, and Immune Cell Mobilisation to Acute Stressors in Young Adults

Ella McLoughlin, Daniel Magistro, Roberto Vagnetti, George Slavich, James Turner, Rachel Arnold, Lee Moore, John Hough

Research output: Contribution to journalArticlepeer-review

Abstract

Many young adults experience mental ill-health which is increasing over time. From a theoretical perspective, the accumulation of stressors experienced over the lifespan may be an important factor in influencing the mental health and well-being of young adults. Although continued exposure to stressors can negatively impact aspects of immunity, researchers have yet to examine how lifetime stressor exposure (i.e., frequency and severity) influences mental ill-health and well-being, and how these states subsequently affected immune cell mobilisation in response to a laboratory-based social stressor in young adults. Eighty-six participants (Mage = 23.31 years, SD = 4.94) completed an online questionnaire which assessed their exposure to lifetime stressors, symptoms of depression and anxiety, and levels of well-being. Next, participants completed the Trier Social Stress Test while immunological (i.e., lymphocytes, monocytes and neutrophils) data were collected immediately pre and post the test. Results revealed that the more frequent and severe stressors experienced during early life rendered individuals more susceptible to stressors during adulthood, which positively influenced symptoms of depression and subsequent anxiety. These aspects then deterred well-being, which negatively affected immune cell mobilisation to the acute stressor. The results highlight the potential importance of assessing lifetime stressor exposure for researchers and clinicians aiming to study the social-environmental drivers of poor immune and clinical health.
Original languageEnglish
Article number101186
JournalBrain Behavior and Immunity - Health
Volume52
Early online date26 Jan 2026
DOIs
Publication statusE-pub ahead of print - 26 Jan 2026

Data Availability Statement

Data will be made available on request.

Funding

G.M.S. was supported by grant #OPR21101 from the California Governor’s Office of Planning and Research/California Initiative to Advance Precision Medicine. This work was supported by the EPSRC and NIHR funds (grant number EP/W031809/1, IMACTIVE). The findings and conclusions in this article are those of the authors and do not necessarily represent the views or opinions of these organisations, which had no role in designing or planning this study; in collecting, analysing, or interpreting the data; in writing the article; or in deciding to submit this article for publication.

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