Positive and negative emotion are associated with generalized transcriptional activation in immune cells
Creators
Abstract
Alterations in immune system gene expression have been implicated in psychopathology, but it remains unclear whether similar associations occur for intraindividual variations in emotion. The present study examined whether positive emotion and negative emotion were related to expression of pro-inflammatory and antiviral genes in circulating leukocytes from a community sample of 90 adolescents (M_(age) = 16.3 years, SD = 0.7; 51.1% female). Adolescents reported their positive emotion and negative emotion and provided blood samples twice, five weeks apart. Using a multilevel analytic framework, we found that within-individual increases in positive emotion were associated with reduced expression of both pro-inflammatory and Type I interferon (IFN) response genes, even after adjusting for demographic and biological covariates, and for leukocyte subset abundance. By contrast, increases in negative emotion were related to higher expression of pro-inflammatory and Type I IFN genes. When tested in the same model, only associations with positive emotion emerged as significant, and increases in overall emotional valence were associated with both lower pro-inflammatory and antiviral gene expression. These results are distinct from the previously observed Conserved Transcriptional Response to Adversity (CTRA) gene regulation pattern characterized by reciprocal changes in pro-inflammatory and antiviral gene expression and may reflect alterations in generalized immunologic activation. These findings highlight one biological pathway by which emotion may potentially impact health and physiological function in the context of the immune system, and future studies can investigate whether fostering positive emotion may promote adolescent health through changes in the immune system.
Additional Information
© 2023 Published by Elsevier Ltd. This work was supported by a grant from Hope Lab to A.J.F. and a consortium seed grant to D.R., S.M.T., and A.J.F. D.R. was supported by a Training Fellowship (1 F31 DA051181–01A1) and the Prevention and Methodology Training Program (PAMT; T32 DA017629) with funding from the National Institute on Drug Abuse of the National Institutes of Health, and S.M.T. was supported by a National Science Foundation Graduate Fellowship (2016207607). The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institute on Drug Abuse, the National Institutes of Health, or the National Science Foundation. CRediT authorship contribution statement: Danny Rahal: Conceptualization, Data curation, Formal analysis, Funding acquisition, Visualization, Writing – original draft. Sarah M. Tashjian: Funding acquisition, Writing – review & editing. Maira Karan: Writing – review & editing. Naomi Eisenberger: Writing – review & editing. Adriana Galván: Writing – review & editing. Andrew J. Fuligni: Funding acquisition, Writing – review & editing. Paul D. Hastings: Funding, Writing – review & editing. Steve W. Cole: Funding acquisition, Visualization, Writing – review & editing. Declarations of interest: None.Attached Files
Supplemental Material - 1-s2.0-S0306453023000811-mmc1.docx
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Additional details
Identifiers
- Eprint ID
- 121617
- Resolver ID
- CaltechAUTHORS:20230530-441700800.45
Funding
- Hope Lab
- NIH Postdoctoral Fellowship
- F31 DA051181-01A1
- NIH Predoctoral Fellowship
- T32 DA017629
- NSF Graduate Research Fellowship
- 2016207607
Dates
- Created
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2023-07-05Created from EPrint's datestamp field
- Updated
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2023-07-05Created from EPrint's last_modified field