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. 2022 Jan;25(1):347-356.
doi: 10.1080/10253890.2022.2148100.

Immune cell dynamics in response to an acute laboratory stressor: a within-person between-group analysis of the biological impact of early life adversity

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Immune cell dynamics in response to an acute laboratory stressor: a within-person between-group analysis of the biological impact of early life adversity

Laura Etzel et al. Stress. 2022 Jan.

Abstract

Early life adversity (ELA) is a risk factor for early onset morbidities and mortality, a relationship that may be driven in part by immune system dysregulation. One mechanism of dysregulation that has yet to be fully examined in the context of ELA is alterations to immune cell dynamics in response to acute stress. Using a within-person between-group experimental design, we investigated stress-induced changes in immune cell populations, and how these changes may be altered in individuals with a history of ELA. Participants were young adults (N = 34, aged 18-25 years, 53% female, 47% with a history of ELA). Complete immune cell counts were measured at four time-points over a 5-hour window across two sessions (Trier Social Stress Test [TSST] vs. no-stress) separated by a week. Across all participants, total white blood cells increased over time (F(3,84)=38.97, p < .001) with a greater increase in response to the TSST compared to the no-stress condition at 240 minutes post-test (b = 0.43±.19; t(179)=2.22, p = .027). This pattern was mirrored by neutrophil counts. Lymphocyte counts were initially depressed by TSST exposure (b =-205±.67; t(184)=-3.07, p = .002) but recovered above baseline. ELA status was associated with higher stress-induced immune cell counts, a difference likely driven by increases in neutrophils (F(1,22)=4.45, p = .046). Overall, these results indicate differential immune cell dynamics in response to acute stress in individuals with a history of ELA. This points to altered immune system functioning in the context of stress, a finding that may be driving increased morbidity and mortality risk for ELA-exposed individuals.

Keywords: Early life adversity; acute stress; immune cell dynamics; psychosocial stress.

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Conflict of interest statement

Disclosure statement

No potential conflict of interest was reported by the author(s).

Figures

Figure 1.
Figure 1.
Study design for both sessions (TSST and no-stress condition). Sessions were separated by one week. Time is denoted as minutes measured from the 15-minute long TSST or resting condition (0 = midway point in session).
Figure 2.
Figure 2.
Total white blood cell counts (Est ± SE) across time within the ELA group vs. control group in the TSST and no-stress sessions. Time is denoted as minutes measured from the 15-minute long TSST or resting condition (0 = midway point of session).
Figure 3.
Figure 3.
Immune cell counts (Est ± SE) across time for ELA-group vs. control-group within the TSST and no-stress conditions. Time is denoted as minutes measured from the 15-minute long TSST or resting condition (0 = midway point of session).

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References

    1. Anda R, Tietjen G, Schulman E, Felitti V, & Croft J (2010). Adverse childhood experiences and frequent headaches in adults. Headache, 50(9), 1473–1481. 10.1111/j.1526-4610.2010.01756.x - DOI - PubMed
    1. Batten SV, Aslan M, Maciejewski PK, & Mazure CM (2004). Childhood maltreatment as a risk factor for adult cardiovascular disease and depression. J Clin Psychiatry, 65(2), 249–254. 10.4088/JCP.v65n0217 - DOI - PubMed
    1. Baumeister D, Akhtar R, Ciufolini S, Pariante CM, & Mondelli V (2016). Childhood trauma and adulthood inflammation: A meta-analysis of peripheral C-reactive protein, interleukin-6 and tumour necrosis factor-α. Molecular Psychiatry, 21(5), 642–649. 10.1038/mp.2015.67 - DOI - PMC - PubMed
    1. Benschop RJ, Rodriguez-Feuerhahn M, & Schedlowski M (1996). Catecholamine-induced leukocytosis: Early observations, current research, and future directions. Brain, Behavior, and Immunity, 10(2), 77–91. 10.1006/brbi.1996.0009 - DOI - PubMed
    1. Born J, Lange T, Hansen K, Molle M, & Fehm HL (1997). Effects of sleep and circadian rhythm on human circulating immune cells. Journal of Immunology, 158(9), 4454–4464. - PubMed

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