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Substantial reduction of naïve and regulatory T cells following traumatic stress
Open accessAbstract
Posttraumatic stress disorder (PTSD) is associated with an enhanced susceptibility to various somatic diseases. However, the exact mechanisms linking traumatic stress to subsequent physical health problems have remained unclear. This study investigated peripheral T lymphocyte differentiation subsets in 19 individuals with war and torture related PTSD compared to 27 non-PTSD controls (n=14 trauma-exposed controls; n=13 non-exposed controls). Peripheral T cell subpopulations were classified by their characteristic expression of the lineage markers CD45RA and CCR7 into: naïve (CD45RA(+) CCR7(+)), central memory (T(CM): CD45RA(-) CCR7(+)) and effector memory (T(EM): CD45RA(-) CCR7(-) and T(EMRA): CD45RA(-) CCR7(-)) cells. Furthermore, we analyzed regulatory T cells (CD4(+)CD25(+)FoxP3(+)) and ex vivo proliferation responses of peripheral blood mononuclear cells after stimulation with anti-CD3 monoclonal antibody. Results show that the proportion of naïve CD8(+) T lymphocytes was reduced by 32% (p=0.01), whereas the proportions of CD3(+) central (p=0.02) and effector (p=0.01) memory T lymphocytes were significantly enhanced (+22% and +34%, respectively) in PTSD patients compared to non-PTSD individuals. To a smaller extent, this effect was also observed in trauma-exposed non-PTSD individuals, indicating a cumulative effect of traumatic stress on T cell distribution. Moreover, PTSD patients displayed a 48% reduction in the proportion of regulatory T cells (p<0.001). Functionally, these alterations were accompanied by a significantly enhanced (+34%) ex vivo proliferation of anti-CD3 stimulated T cells (p=0.05). The profoundly altered composition of the peripheral T cell compartment might cause a state of compromised immune responsiveness, which may explain why PTSD patients show an increased susceptibility to infections, and inflammatory and autoimmune diseases.
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“Individuals with PTSD also have reduced numbers of naive CD8(+) T lymphocytes and increases in the proportions of CD3(+) central and effector memory T lymphocytes compared with individuals without PTSD (Sommershof et al, 2009).”
From Inflammation in Fear- and Anxiety-Based Disorders: PTSD, GAD, and Beyond (2017) · cites this paper as Sommershof et al, 2009
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Cites
Hamilton, M. (1960) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.23.1.56 · Cited by 32,817
(1998) · The Journal of Clinical Psychiatry · Cited by 19,139
Diagnostic and Statistical Manual of Mental Disorders (DSM-IV)
Hu, R. J. (2003) · Elsevier eBooks · doi:10.1016/b0-12-226870-9/01070-4 · Cited by 9,168
Foxp3 programs the development and function of CD4+CD25+ regulatory T cells
Fontenot, J. D., Gavin, M. A., & Rudensky, A. Y. (2003) · Nature Immunology · doi:10.1038/ni904 · Cited by 7,745
Two subsets of memory T lymphocytes with distinct homing potentials and effector functions
Sallusto, F., Lenig, D., Förster, R., Lipp, M., & Lanzavecchia, A. (1999) · Nature · doi:10.1038/44385 · Cited by 5,846 · cited 9×
“According to this model, naïve T cells (CD45RA + CCR7 + ) become activated after antigen stimulation, then differentiate into memory cells, and partly develop into effector cells with a strong cytolytic capability (Hamann et al., 1999; Sallusto et al., 1999).”
InfluentialThe development of a Clinician-Administered PTSD Scale
Blake, D. D., Weathers, F. W., Nagy, L. M., Kaloupek, D. G., Gusman, F. D., Charney, D. S., & Keane, T. M. (1995) · Journal of Traumatic Stress · doi:10.1002/jts.2490080106 · Cited by 5,024
Vignali, D. A. A., Collison, L. W., & Workman, C. J. (2008) · Nature Reviews Immunology · doi:10.1038/nri2343 · Cited by 3,463
Central Memory and Effector Memory T Cell Subsets: Function, Generation, and Maintenance
Sallusto, F., Geginat, J., & Lanzavecchia, A. (2004) · Annual Review of Immunology · doi:10.1146/annurev.immunol.22.012703.104702 · Cited by 3,067
Accelerated telomere shortening in response to life stress
Epel, E. S., Blackburn, E. H., Lin, J., Dhabhar, F. S., Adler, N. E., Morrow, J. D., & Cawthon, R. M. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0407162101 · Cited by 3,002
An essential role for Scurfin in CD4+CD25+ T regulatory cells
Khattri, R., Cox, T., Yasayko, S.-A., & Ramsdell, F. (2003) · Nature Immunology · doi:10.1038/ni909 · Cited by 2,860
Chronic stress and age-related increases in the proinflammatory cytokine IL-6.
Kiecolt-Glaser, J. K., Preacher, K. J., MacCallum, R. C., Atkinson, C., Malarkey, W. B., & Glaser, R. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1531903100 · Cited by 1,267 · cited 2×
“, 2004) and thus is consistent with other reports showing that psychological stress is associated with immunological aging (Bosch et al., 2009; Epel et al., 2004; Kiecolt-Glaser et al., 2003).”
Homeostasis and Self-Tolerance in the Immune System: Turning Lymphocytes off
Parijs, L. V., & Abbas, A. K. (1998) · Science · doi:10.1126/science.280.5361.243 · Cited by 958
National Collaborating Centre for Mental Health
Veale, D. M. (2006) · Research Portal (King's College London) · Cited by 941
Ziegler, S. F. (2005) · Annual Review of Immunology · doi:10.1146/annurev.immunol.24.021605.090547 · Cited by 921
Autonomic innervation and regulation of the immune system (1987–2007)
Nance, D. M., & Sanders, V. M. (2007) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2007.03.008 · Cited by 855
McEwen, B. S., Biron, C. A., Brunson, K. W., Bulloch, K., Chambers, W. H., Dhabhar, F. S., Goldfarb, R. H., Kitson, R. P., Miller, A. H., Spencer, R. L., et al. (1997) · Brain Research Reviews · doi:10.1016/s0165-0173(96)00012-4 · Cited by 837
Cutting Edge: Control of CD8+ T Cell Activation by CD4+CD25+ Immunoregulatory Cells
Piccirillo, C. A., & Shevach, E. M. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.3.1137 · Cited by 716
Permutation, Parametric and Bootstrap Tests of Hypotheses
(2005) · Springer Series in Statistics · doi:10.1007/b138696 · Cited by 707
Regulatory T cells: friend or foe in immunity to infection?
Mills, K. H. G. (2004) · Nature reviews. Immunology · doi:10.1038/nri1485 · Cited by 702
Posttraumatic stress disorder and physical illness: results from clinical and epidemiologic studies
BOSCARINO, J. A. (2004) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1314.011 · Cited by 691
(2000) · PubMed · Cited by 676
Shortage of circulating naive CD8+ T cells provides new insights on immunodeficiency in aging
Fagnoni, F. F., Vescovini, R., Passeri, G., Bologna, G., Pedrazzoni, M., Lavagetto, G., Casti, A., Franceschi, C., Passeri, M., & Sansoni, P. (2000) · Blood · doi:10.1182/blood.v95.9.2860.009k35_2860_2868 · Cited by 515
Neuner, F., Schauer, M., Karunakara, U. K., Klaschik, C., Robert, C., & Elbert, T. R. (2004) · BMC Psychiatry · doi:10.1186/1471-244x-4-34 · Cited by 466
Self-citationPosttraumatic Stress Symptoms, Intrusive Thoughts, Loss, and Immune Function after Hurricane Andrew
Ironson, G. H., Wynings, C., Schneiderman, N., Baum, A. E., Rodriguez, M. S., Greenwood, D., Benight, C. C., Antoni, M. H., LaPerriere, A. R., Huang, H.-S., et al. (1997) · Psychosomatic Medicine · doi:10.1097/00006842-199703000-00003 · Cited by 444
Neuner, F., Onyut, P. L., Ertl, V., Odenwald, M., Schauer, E., & Elbert, T. (2008) · Journal of Consulting and Clinical Psychology · doi:10.1037/0022-006x.76.4.686 · Cited by 395 · cited 2×
“In a recent study, we demonstrated that successful treatment – in this case by means of Narrative Exposure Therapy – also significantly reduced cough, diarrhoea, and fever (Neuner et al., 2008 ).”
Self-citationSareen, J., Cox, B. J., Clara, I., & Asmundson, G. J. G. (2005) · Depression and Anxiety · doi:10.1002/da.20072 · Cited by 389
Physical health and post-traumatic stress disorder: review and synthesis.
Schnurr, P. P., & Jankowski, M. K. (1999) · PubMed · Cited by 239
Health Care Costs Associated With Posttraumatic Stress Disorder Symptoms in Women
Walker, E. A., Katon, W. J., Russo, J. E., Ciechanowski, P. S., Newman, E., & Wagner, A. W. (2003) · Archives of General Psychiatry · doi:10.1001/archpsyc.60.4.369 · Cited by 234
CD25+CD4+ T cells contribute to the control of memory CD8+ T cells
Murakami, M., Sakamoto, A., Bender, J., Kappler, J. W., & Marrack, P. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.132254399 · Cited by 234
Suppression of Cellular Immunity in Men With a Past History of Posttraumatic Stress Disorder
Kawamura, N., Kim, Y., & Asukai, N. (2001) · American Journal of Psychiatry · doi:10.1176/appi.ajp.158.3.484 · Cited by 225
Weisberg, R. B., Bruce, S. E., Machan, J. T., Kessler, R. C., Culpepper, L., & Keller, M. B. (2002) · Psychiatric Services · doi:10.1176/appi.ps.53.7.848 · Cited by 198
Neurotransmitter alterations in PTSD: catecholamines and serotonin.
Southwick, S. M., Paige, S. R., Morgan, C. A., Bremner, J. D., Krystal, J. H., & Charney, D. S. (1999) · PubMed · Cited by 196
Lindauer, R., Olff, M., van Meijel, E. P. M., Carlier, I. V. E., & Gersons, B. P. R. (2005) · Biological Psychiatry · doi:10.1016/j.biopsych.2005.06.033 · Cited by 188
Faces and phases of human CD8+ T-cell development
Hamann, D., Roos, M. T. L., & van Lier, R. A. W. (1999) · Immunology Today · doi:10.1016/s0167-5699(99)01444-9 · Cited by 179
IPEX, FOXP3 and regulatory T-cells: a model for autoimmunity
Ochs, H. D., Gambineri, E., & Torgerson, T. R. (2007) · Immunologic Research · doi:10.1007/s12026-007-0022-2 · Cited by 176
Human regulatory T cells and autoimmunity
Costantino, C. M., Baecher‐Allan, C., & Hafler, D. A. (2008) · European Journal of Immunology · doi:10.1002/eji.200738104 · Cited by 158
Structural and Functional Neuroplasticity in Relation to Traumatic Stress
Kolassa, I., & Elbert, T. R. (2007) · Current Directions in Psychological Science · doi:10.1111/j.1467-8721.2007.00529.x · Cited by 141
Self-citationHug, A., Korporal, M., Schröder, I., Haas, J., Glatz, K., Storch-Hagenlocher, B., & Wildemann, B. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.171.1.432 · Cited by 139
Thymic function and peripheral T-cell homeostasis in rheumatoid arthritis
Goronzy, J. J., & Weyand, C. M. (2001) · Trends in Immunology · doi:10.1016/s1471-4906(00)01841-x · Cited by 137
Boscarino, J. A., & Chang, J. (1999) · Psychosomatic Medicine · doi:10.1097/00006842-199905000-00019 · Cited by 136
Age-associated changes in the frequency of naïve, memory and effector CD8+ T cells
Hong, M. S., Dan, J. M., Choi, J.-Y., & Kang, I. (2004) · Mechanisms of Ageing and Development · doi:10.1016/j.mad.2004.07.001 · Cited by 107
Bosch, J. A., Fischer, J. E., & Fischer, J. (2009) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2009.02.002 · Cited by 96
Control of homeostatic proliferation by regulatory T cells
Shen, S. S. (2005) · Journal of Clinical Investigation · doi:10.1172/jci25463 · Cited by 91
Phenotype of Blood Lymphocytes in PTSD Suggests Chronic Immune Activation
Wilson, S. N., van der Kolk, B. A., Burbridge, J. A., Fisler, R. E., & Kradin, R. L. (1999) · Psychosomatics · doi:10.1016/s0033-3182(99)71238-7 · Cited by 88
Laudenslager, M. L., Aasal, R., Adler, L. E., Berger, C. L., Montgomery, P. T., Sandberg, E., Wahlberg, L., Wilkins, R. T., Zweig, L., & Reite, M. L. (1998) · Brain Behavior and Immunity · doi:10.1006/brbi.1997.0513 · Cited by 83
Altemus, M. M., Dhabhar, F. S., & Yang, R. (2006) · Annals of the New York Academy of Sciences · doi:10.1196/annals.1364.013 · Cited by 67
Vidović, A., Vilibić, M., Sabioncello, A., Gotovac, K., Rabatić, S., Folnegović-Šmalc, V., & Dekaris, D. (2007) · PubMed Central · Cited by 53
Duszczyszyn, D. A., Beck, J., Antel, J. P., Bar‐Or, A., Lapierre, Y., Gadag, V. G., & Haegert, D. G. (2005) · Clinical & Experimental Immunology · doi:10.1111/j.1365-2249.2005.02990.x · Cited by 51
Kimerling, R. E. (2004) · PubMed · Cited by 41
No PTSD-related differences in diurnal cortisol profiles of genocide survivors
Eckart, C., Engler, H., Riether, C., Kolassa, S., Elbert, T. R., & Kolassa, I. (2008) · Psychoneuroendocrinology · doi:10.1016/j.psyneuen.2008.10.012 · Cited by 37
Self-citationGlover, D. A., Steele, A. C., Stuber, M. L., & Fahey, J. L. (2004) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2004.08.002 · Cited by 32
The mental health disaster in conflict settings: Can scientific research help?
Neuner, F., & Elbert, T. R. (2007) · BMC Public Health · doi:10.1186/1471-2458-7-275 · Cited by 27
Self-citationEndocrine and inflammatory alterations in post-traumatic stress disorder
Wessa, M., & Rohleder, N. (2006) · Expert Review of Endocrinology & Metabolism · doi:10.1586/17446651.2.1.91 · Cited by 26
Effect of age on thymic development, T cell immunity, and helper T cell function
Shen, S. S., Kim, J. S., & Weksler, M. E. (2005) · Springer eBooks · doi:10.1007/bfb0033650 · Cited by 18
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Metadata
- Authors
- Sommershof, A., Aichinger, H., Engler, H., Adenauer, H., Catani, C., Boneberg, E.-M., Elbert, T., Groettrup, M., & Kolassa, I.-T.
- Affiliations
- University of Konstanz (DE)
- Essen University Hospital (DE)
- Bielefeld University (DE)
- Venue
- Brain, Behavior, and Immunity
- Publisher
- Elsevier BV
- Published
- 2009-11
- Volume
- 23
- Issue
- 8
- Pages
- 1117-1124
- ISSN
- 0889-1591 (ISSN-L)
- OpenAlex
- W1982301384
- Semantic Scholar
- 23eda2aa2cfa505a1b93574b87c419c3c31454ba
- Cited by
- 172
- References
- 55
- Citations by year
- 2026: 5 · 2025: 7 · 2024: 8 · 2023: 10 · 2022: 15 · 2021: 7 · 2020: 11 · 2019: 7 · 2018: 15 · 2017: 12 · 2016: 15 · 2015: 11 · 2014: 9 · 2013: 11 · 2012: 8
- FWCI
- 10.24
- Type
- journal article
- Language
- en
- Open access
- green
- nbn-resolving.de
- Locations
- Brain Behavior and Immunity (publishedVersion)
- PubMed (publishedVersion)
- KOPS (University of Konstanz) (submittedVersion)
- Funders
- Deutsche Forschungsgemeinschaft (FOR751)
- European Refugee Fund
- Topics
- Social Sciences › Psychology › Clinical Psychology › Posttraumatic Stress Disorder Research
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Keywords
- post-traumatic stress disorder, traumatic stress, T cell differentiation, naive T cells, regulatory T cells, central memory T cells, effector memory T cells, CD45RA, CCR7, T cell proliferation, immune dysfunction, trauma-exposed individuals
- MeSH terms
- Adult, Analysis of Variance, Cell Count, Combat Disorders, Female, Flow Cytometry, Humans, Immunologic Memory, Lymphocyte Activation, Male, Middle Aged, Psychological Tests, Stress Disorders, Post-Traumatic, T-Lymphocytes, Cell Lineage, Cell Proliferation
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