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Glucocorticoids and the Th1/Th2 Balance
Abstract
A bstract: Evidence accumulated over the last 5‐10 years indicates that glucocorticoids (GCs) inhibit the production of interleukin (IL)‐12, interferon (IFN)‐γ, IFN‐α, and tumor necrosis factor (TNF)‐α by antigen‐presenting cells (APCs) and T helper (Th)1 cells, but upregulate the production of IL‐4, IL‐10, and IL‐13 by Th2 cells. Through this mechanism increased levels of GCs may systemically cause a selective suppression of the Th1‐cellular immunity axis, and a shift toward Th2‐mediated humoral immunity, rather than generalized immunosuppression. During an immune response and inflammation, the activation of the stress system, and thus increased levels of systemic GCs through induction of a Th2 shift, may actually protect the organism from systemic “overshooting” with Th1/pro‐inflammatory cytokines and other products of activated macrophages with tissue‐damaging potential. However, conditions associated with significant changes of GCs levels, such as acute or chronic stress or cessation of chronic stress, severe exercise, and pregnancy and postpartum, through modulation of the Th1/Th2 balance may affect the susceptibility to or the course of infections as well as autoimmune and atopic/allergic diseases.
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Cites
The Hypothalamic–Pituitary–Adrenal Axis and Immune-Mediated Inflammation
Chrousos, G. P. (1995) · New England Journal of Medicine · doi:10.1056/nejm199505183322008 · Cited by 2,579
Psychological Stress and Susceptibility to the Common Cold
Cohen, S., Tyrrell, D. A. J., & Smith, A. P. (1991) · New England Journal of Medicine · doi:10.1056/nejm199108293250903 · Cited by 1,712
Stress Hormones, Proinflammatory and Antiinflammatory Cytokines, and Autoimmunity
ELENKOV, I. J., & CHROUSOS, G. P. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb04229.x · Cited by 983
Self-citationKristo, C., Godang, K., Ueland, T., Lien, E., Aukrust, P., Froland, S., & Bollerslev, J. (2002) · European Journal of Endocrinology · doi:10.1530/eje.0.1460389 · Cited by 45
Cited by
Exploring the full spectrum of macrophage activation
Mosser, D. M., & Edwards, J. P. (2008) · Nature Reviews Immunology · doi:10.1038/nri2448 · Cited by 9,144
Immune regulation by glucocorticoids
Cain, D. W., & Cidlowski, J. A. (2017) · Nature Reviews Immunology · doi:10.1038/nri.2017.1 · Cited by 1,846
Annexin A1 and glucocorticoids as effectors of the resolution of inflammation
Perretti, M., & D'Acquisto, F. (2009) · Nature Reviews Immunology · doi:10.1038/nri2470 · Cited by 915
Dhabhar, F. S. (2009) · Neuroimmunomodulation · doi:10.1159/000216188 · Cited by 903
Stress and the hypothalamic pituitary adrenal axis in the developmental course of schizophrenia
Walker, E., Mittal, V., & Tessner, K. (2008) · Annual Review of Clinical Psychology · doi:10.1146/annurev.clinpsy.4.022007.141248 · Cited by 615
Pain and Stress in a Systems Perspective: Reciprocal Neural, Endocrine, and Immune Interactions
Chapman, C. R., Tuckett, R. P., & Song, C. W. (2008) · The Journal of Pain · doi:10.1016/j.jpain.2007.09.006 · Cited by 541
Exercise and the aging immune system
Simpson, R. J., Lowder, T. W., Spielmann, G., Bigley, A. B., LaVoy, E. C., & Kunz, H. (2012) · Ageing Research Reviews · doi:10.1016/j.arr.2012.03.003 · Cited by 281
PTSD is associated with an excess of inflammatory immune activities
Gill, J. M., Saligan, L., Woods, S., & Page, G. (2009) · Perspectives in Psychiatric Care · doi:10.1111/j.1744-6163.2009.00229.x · Cited by 271
Low cortisol, high DHEA, and high levels of stimulated TNF‐α, and IL‐6 in women with PTSD
Gill, J., Vythilingam, M., & Page, G. G. (2008) · Journal of Traumatic Stress · doi:10.1002/jts.20372 · Cited by 240
Marques, A. H., O'Connor, T. G., Roth, C., Susser, E., & Bjørke-Monsen, A.-L. (2013) · Frontiers in Neuroscience · doi:10.3389/fnins.2013.00120 · Cited by 226
Glucocorticoid Dysregulations and Their Clinical Correlates: From Receptors to Therapeutics
Marques, A. H., Silverman, M. N., & Sternberg, E. M. (2009) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2009.04987.x · Cited by 158
Glucocorticoid modulation of cytokine signaling
Rogatsky, I., & Ivashkiv, L. B. (2006) · Tissue Antigens · doi:10.1111/j.1399-0039.2006.00599.x · Cited by 150
The GRIP1:IRF3 interaction as a target for glucocorticoid receptor-mediated immunosuppression
Reily, M. M., Pantoja, C., Hu, X., Chinenov, Y., & Rogatsky, I. (2006) · The EMBO Journal · doi:10.1038/sj.emboj.7600919 · Cited by 149
Hernández, M. E., Mendieta, D., Martínez-Fong, D., Loría, F., Moreno, J., Estrada, I., Bojalil, R., & Pavón, L. (2008) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2008.08.001 · Cited by 140
Minireview: glucocorticoids in autoimmunity: unexpected targets and mechanisms
Flammer, J. R., & Rogatsky, I. (2011) · Molecular Endocrinology · doi:10.1210/me.2011-0068 · Cited by 140
Influence of prenatal psychosocial stress on cytokine production in adult women
Entringer, S., Kumsta, R., Nelson, E. L., Hellhammer, D. H., Wadhwa, P. D., & Wüst, S. (2008) · Developmental Psychobiology · doi:10.1002/dev.20316 · Cited by 127
Depressed and anxious mood and T-cell cytokine expressing populations in ovarian cancer patients
Lutgendorf, S. K., Lamkin, D. M., DeGeest, K., Anderson, B., Dao, M., McGinn, S., Zimmerman, B., Maiseri, H., Sood, A. K., & Lubaroff, D. M. (2008) · Brain, Behavior, and Immunity · doi:10.1016/j.bbi.2007.12.012 · Cited by 126
Are Maternal Cortisol Levels Related to Preterm Birth?
Giurgescu, C. (2009) · Journal of Obstetric, Gynecologic & Neonatal Nursing · doi:10.1111/j.1552-6909.2009.01034.x · Cited by 116
Martino, M., Rocchi, G., Escelsior, A., & Fornaro, M. (2012) · Current Neuropharmacology · doi:10.2174/157015912800604542 · Cited by 111
Stress and coping in women with breast cancer:unravelling the mechanisms to improve resilience
Borgi, M., Collacchi, B., Ortona, E., & Cirulli, F. (2020) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2020.10.011 · Cited by 90
Host Competence: An Organismal Trait to Integrate Immunology and Epidemiology
Martin, L. B., Burgan, S. C., Adelman, J. S., & Gervasi, S. S. (2016) · Integrative and Comparative Biology · doi:10.1093/icb/icw064 · Cited by 83
Effects of Maternal Prenatal Stress on Infant Outcomes: A Synthesis of the Literature
Ruiz, R. J., & Avant, K. C. (2005) · Advances in Nursing Science · doi:10.1097/00012272-200510000-00006 · Cited by 79
Craddock, T. J. A., Fritsch, P., Rice, M. A., del Rosario, R. M., Miller, D. B., Fletcher, M. A., Klimas, N. G., & Broderick, G. (2014) · PLoS ONE · doi:10.1371/journal.pone.0084839 · Cited by 75
Telomere shortening and immune activity in war veterans with posttraumatic stress disorder
Jergović, M., Tomičević, M., Vidović, A., Bendelja, K., Savić, A., Vojvoda, V., Rac, D., Lovrić-Čavar, D., Rabatić, S., Jovanovic, T., et al. (2014) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2014.06.010 · Cited by 67
Harpaz, I., Abutbul, S., Nemirovsky, A., Gal, R., Cohen, H., & Monsonego, A. (2013) · European Journal of Immunology · doi:10.1002/eji.201242613 · Cited by 64
Viveros-Paredes, J. M., Puebla-Pérez, A. M., Gutiérrez-Coronado, O., Sandoval-Ramírez, L., & Villaseñor-García, M. M. (2006) · International Immunopharmacology · doi:10.1016/j.intimp.2005.11.011 · Cited by 62
Fornaro, M., Rocchi, G., Escelsior, A., Contini, P., & Martino, M. (2013) · Journal of Affective Disorders · doi:10.1016/j.jad.2012.08.007 · Cited by 59
Cortisol awakening response is linked to disease course and progression in multiple sclerosis
Kern, S., Krause, I., Horntrich, A., Thomas, K., Aderhold, J., & Ziemssen, T. (2013) · PLoS ONE · doi:10.1371/journal.pone.0060647 · Cited by 50
The effects of an anticipated challenge on diurnal cortisol secretion
Wetherell, M. A., Lovell, B., & Smith, M. A. (2015) · Stress · doi:10.3109/10253890.2014.993967 · Cited by 50
Plasma interleukin-6 and executive function in crack cocaine-dependent women.
Levandowski, M. L., Hess, A. R. B., Grassi-Oliveira, R., & de Almeida, R. M. M. (2016) · Neuroscience Letters · doi:10.1016/j.neulet.2016.06.023 · Cited by 45
Miljković, Ž., Momčilović, M., Miljković, D., & Mostarica-Stojković, M. (2009) · Journal of Neuroinflammation · doi:10.1186/1742-2094-6-37 · Cited by 35
Glucocorticoids and natural killer cells: A suppressive relationship
Muscari, I., Fierabracci, A., Adorisio, S., Moretti, M., Cannarile, L., Thi Minh Hong, V., Ayroldi, E., & Delfino, D. V. (2022) · Biochemical Pharmacology · doi:10.1016/j.bcp.2022.114930 · Cited by 32
Merk, V. M., Phan, T. S., & Brunner, T. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.672808 · Cited by 27
Kurczewska, E., Ferensztajn-Rochowiak, E., Jasińska-Mikołajczyk, A., Chłopocka-Woźniak, M., & Rybakowski, J. K. (2019) · Pharmacopsychiatry · doi:10.1055/a-0695-9138 · Cited by 17
Xiang, L., Rehm, K. E., Sunesara, I., Griswold, M., & Marshall, G. D. (2015) · Journal of Psychosomatic Research · doi:10.1016/j.jpsychores.2014.11.004 · Cited by 6
Metadata
- Authors
- ELENKOV, I. J.
- Venue
- Annals of the New York Academy of Sciences
- Publisher
- Wiley
- Published
- 2004-06
- Volume
- 1024
- Issue
- 1
- Pages
- 138-146
- ISSN
- 0077-8923 (ISSN-L)
- 1749-6632
- OpenAlex
- W2167012568
- Cited by
- 612
- References
- 4
- FWCI
- 7.64
- Type
- journal article
- Language
- en
- Open access
- closed
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