Social-evaluative threat and proinflammatory cytokine regulation: an experimental laboratory investigation.

TitleSocial-evaluative threat and proinflammatory cytokine regulation: an experimental laboratory investigation.
Publication TypeJournal Article
Year of Publication2009
AuthorsDickerson SS, Gable SL, Irwin MR, Aziz N, Kemeny ME
JournalPsychol Sci
Volume20
Issue10
Pagination1237-44
Date Published2009 Oct
ISSN1467-9280
KeywordsAdult, Analysis of Variance, Blood Pressure, Cytokines, Emotions, Female, Glucocorticoids, Humans, Mathematics, Self Concept, Social Behavior, Speech, Stress, Psychological, Surveys and Questionnaires, Task Performance and Analysis, Tumor Necrosis Factor-alpha, Young Adult
Abstract

This study experimentally tested whether a stressor characterized by social-evaluative threat (SET), a context in which the self can be judged negatively by others, would elicit increases in proinflammatory cytokine activity and alter the regulation of this response. This hypothesis was derived in part from research on immunological responses to social threat in nonhuman animals. Healthy female participants were assigned to perform a speech and a math task in the presence or absence of an evaluative audience (SET or non-SET, respectively). As hypothesized, stimulated production of the proinflammatory cytokine tumor necrosis factor-alpha (TNF-alpha) increased from baseline to poststressor in the SET condition, but was unchanged in the non-SET condition. Further, the increases in TNF-alpha production correlated with participants' cognitive appraisals of being evaluated. Additionally, the ability of glucocorticoids to shut down the inflammatory response was decreased in the SET condition. These findings underscore the importance of social evaluation as a threat capable of eliciting proinflammatory cytokine activity and altering its regulation.

DOI10.1111/j.1467-9280.2009.02437.x
Alternate JournalPsychol Sci
PubMed ID19754527
PubMed Central IDPMC2761517
Grant ListM01 RR000865-328463 / RR / NCRR NIH HHS / United States
M01-RR00865 / RR / NCRR NIH HHS / United States