Blood levels of T-Cell Receptor Excision Circles (TRECs) provide an index of exposure to traumatic stress in mice and humans

• Published in: Translational psychiatry 2022-10, Vol.12 (1), p.423-423, Article 423
• Main Authors: McCullough, Kenneth M., Katrinli, Seyma, Hartmann, Jakob, Lori, Adriana, Klengel, Claudia, Missig, Galen, Klengel, Torsten, Langford, Nicole A., Newman, Emily L., Anderson, Kasey J., Smith, Alicia K., Carroll, F. Ivy, Ressler, Kerry J., Carlezon, William A.
• Format: Article
• Language: English
• Subjects: 631/443; 64; 64/60; 692/53; Animals; Behavioral Sciences; Biological Psychology; Biomarkers; Biomarkers - analysis; Blood; Child; Depressive Disorder, Major - genetics; DNA, Circular; Humans; Male; Mammals - genetics; Medicine; Medicine & Public Health; Mice; Neurosciences; Pharmacotherapy; Physiology; Psychiatry; Receptors, Antigen, T-Cell - genetics; Stress; T-Lymphocytes; Thymus gland
• ISSN: 2158-3188; 2158-3188
• DOI: 10.1038/s41398-022-02159-7

Exposure to stress triggers biological changes throughout the body. Accumulating evidence indicates that alterations in immune system function are associated with the development of stress-associated illnesses such as major depressive disorder and post-traumatic stress disorder, increasing interest in identifying immune markers that provide insight into mental health. Recombination events during T-cell receptor rearrangement and T-cell maturation in the thymus produce circular DNA fragments called T-cell receptor excision circles (TRECs) that can be utilized as indicators of thymic function and numbers of newly emigrating T-cells. Given data suggesting that stress affects thymus function, we examined whether blood levels of TRECs might serve as a quantitative peripheral index of cumulative stress exposure and its physiological correlates. We hypothesized that chronic stress exposure would compromise thymus function and produce corresponding decreases in levels of TRECs. In male mice, exposure to chronic social defeat stress (CSDS) produced thymic involution, adrenal hypertrophy, and decreased levels of TRECs in blood. Extending these studies to humans revealed robust inverse correlations between levels of circulating TRECs and childhood emotional and physical abuse. Cell-type specific analyses also revealed associations between TREC levels and blood cell composition, as well as cell-type specific methylation changes in CD4T + and CD8T + cells. Additionally, TREC levels correlated with epigenetic age acceleration, a common biomarker of stress exposure. Our findings demonstrate alignment between findings in mice and humans and suggest that blood-borne TRECs are a translationally-relevant biomarker that correlates with, and provides insight into, the cumulative physiological and immune-related impacts of stress exposure in mammals.