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Issue 1071 coverPSYCHOBIOLOGY OF POSTTRAUMATIC STRESS DISORDER A Decade of Progress Volume 1071 published July 2006
Ann. N.Y. Acad. Sci. 1071: 167–183 (2006). doi: 10.1196/annals.1364.013
Copyright © 2006 by the New York Academy of Sciences
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Articles by ALTEMUS, M.
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Immune Function in PTSD

MARGARET ALTEMUSa, FIRDAUS S. DHABHARb AND RUIRONG YANGa

a Department of Psychiatry, Weill Medical College, Cornell University, New York, New York 10021, USA b Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, California 94305, USA

Key Words: PTSD • stress • skin • immune function • skin barrier function • immune cells

Address for correspondence: Margaret Altemus, M.D., Department of Psychiatry, Weill Medical College, Cornell University, Box 244, 1300 York Ave, New York, NY 10021. Voice: 212-746-3751; fax: 212-746-3870.  e-mail: maltemus{at}med.cornell.edu

Disturbed regulation of both the hypothalamic-pituitary-adrenal (HPA) axis and sympathoadrenomedullary system in posttraumatic stress disorder (PTSD) suggests that immune function, which is modulated by these systems, may also be dysregulated. Two dermatologic, in vivo measures of immune function, delayed-type hypersensitivity (DTH) and skin barrier function recovery, were examined in female subjects with PTSD and compared to measures in healthy female comparison subjects. In addition, at the time of DTH test placement, circulating numbers of lymphocyte subtypes were assessed. In separate studies, the effects of acute psychological stress on DTH and skin barrier function recovery were examined in healthy volunteer subjects. Both DTH and barrier function recovery were enhanced in women with PTSD. These findings contrast with the effects of acute stress in healthy control subjects, which was associated with suppression of DTH responses and skin barrier function recovery. There was no difference between subjects with PTSD and healthy control subjects in proportions of circulating lymphocyte subsets or in expression of the lymphocyte markers CD62, CD25, and CD45RO/CD45RA. These results suggest that cell-mediated immune function is enhanced in individuals with PTSD, a condition that imposes chronic physiologic and mental stress on sufferers. These findings contrast with suppression of DTH and skin barrier function recovery in healthy volunteers in response to acute psychological stress.






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