Dehydroepiandrosterone as a regulator of immune cell function

Age changes and sex differences in serum dehydroepiandrosterone sulfate concentrations throughout adulthood

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Altered regulation of IL-6 production with normal aging. Possible linkage to the age-associated decline in dehydroepiandrosterone and its sulfated derivative

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The aging immune system: primer and prospectus

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Association between premature mortality and hypopituitarism

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11β-Hydroxysteroid dehydrogenase type 1: a tissue specific regulator of glucocorticoid response

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Psychoneuroendocrine influences on immunocompetence and neoplasia

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Marked decline in serum concentrations of adrenal C19 sex steroid precursors and conjugated androgen metabolites during aging

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Dehydroepiandrosterone Replacement in Women with Adrenal Insufficiency

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Peroxisome Proliferator-activated Receptor α Activation Modulates Cellular Redox Status, Represses Nuclear Factor-κB Signaling, and Reduces Inflammatory Cytokine Production in Aging

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11β-Hydroxysteroid Dehydrogenase and the Syndrome of Apparent Mineralocorticoid Excess*

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Human innate immunosenescence: causes and consequences for immunity in old age

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Senescence in innate immune responses: reduced neutrophil phagocytic capacity and CD16 expression in elderly humans

Butcher, S. K., Chahal, H., Nayak, L., Sinclair, A., Henriquez, N. V., Sapey, E., O'Mahony, D., & Lord, J. M. (2001) · Journal of Leukocyte Biology · doi:10.1189/jlb.70.6.881 · Cited by 436 · see citing works

Long-term longitudinal measurements of plasma dehydroepiandrosterone sulfate in normal men

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Contrasting effects of glucocorticoids on the capacity of T cells to produce the growth factors interleukin 2 and interleukin 4

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Serum Dehydroepiandrosterone (DHEA) and DHEA Sulfate Are Negatively Correlated with Serum Interleukin-6 (IL-6), and DHEA Inhibits IL-6 Secretion from Mononuclear Cells in Man in Vitro: Possible Link between Endocrinosenescence and Immunosenescence

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Age and sex related differences in serum levels of unconjugated dehydroepiandrosterone and its sulphate in normal subjects

Šulcová, J., Hill, M., Hampl, R., & Stárka, L. (1997) · Journal of Endocrinology · doi:10.1677/joe.0.1540057 · Cited by 327 · see citing works

Regulation of murine lymphokine production in vivo II. Dehydroepiandrosterone is a natural enhancer of interleukin 2 synthesis by helper T cells

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In vivo production of interleukin‐10 by non–t cells in rheumatoid arthritis, sjöugren's syndrome, and systemic lupus erythematosus.

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Nongenomic Stimulation of Nitric Oxide Release by Estrogen Is Mediated by Estrogen Receptor α Localized in Caveolae

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Evidence for Adrenocortical Adaptation to Severe Illness*

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Dehydroepiandrosterone Activates Endothelial Cell Nitric-oxide Synthase by a Specific Plasma Membrane Receptor Coupled to Gαi2,3

Liu, D., & Dillon, J. S. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m200491200 · Cited by 285 · see citing works

Dehydroepiandrosterone enhances IL2 production and cytotoxic effector function of human T cells.

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Adrenal glands of mouse and rat do not synthesize androgens

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Dehydroepiandrosterone and androsterone levels in human plasma. Effect of age and sex: day-to-day and diurnal variations.

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The Biological Actions of Dehydroepiandrosterone Involves Multiple Receptors

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Cyp7b, a novel brain cytochrome P450, catalyzes the synthesis of neurosteroids 7α-hydroxy dehydroepiandrosterone and 7α-hydroxy pregnenolone

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The zona reticularis is the site of biosynthesis of dehydroepiandrosterone and dehydroepiandrosterone sulfate in the adult human adrenal cortex resulting from its low expression of 3 beta-hydroxysteroid dehydrogenase.

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Dehydroepiandrosterone Antagonizes the Suppressive Effects of Dexamethasone on Lymphocyte Proliferation*

Blauer, K. L., Poth, M., ROGERS, W. M., & Bernton, E. W. (1991) · Endocrinology · doi:10.1210/endo-129-6-3174 · Cited by 217 · see citing works

Oral dehydroepiandrosterone in physiologic doses modulates immune function in postmenopausal women

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Challenges for vaccination in the elderly

Aspinall, R., Giudice, G. D., Effros, R. B., Grubeck‐Loebenstein, B., & Sambhara, S. R. (2007) · Immunity & Ageing · doi:10.1186/1742-4933-4-9 · Cited by 205 · see citing works

Oral dehydroepiandrosterone for adrenal androgen replacement: pharmacokinetics and peripheral conversion to androgens and estrogens in young healthy females after dexamethasone suppression

Arlt, W., Justl, H.-G., Callies, F., Reincke, M., Hübler, D., Oettel, M., Ernst, M., Schulte, H. M., & Allolio, B. (1998) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.83.6.4850 · Cited by 199 · see citing works

The presence of a dehydroepiandrosterone-specific receptor binding complex in murine T cells

Meikle, A. W., Dorchuck, R. W., Araneo, B. A., Stringham, J. D., Evans, T. G., Spruance, S. L., & Daynes, R. A. (1992) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/0960-0760(92)90132-3 · Cited by 186 · see citing works

Protection against acute lethal viral infections with the native steroid dehydroepiandrosterone (DHEA)

Loria, R. M., Inge, T. H., Cook, S. S., Szakal, A. K., & Regelson, W. (1988) · Journal of Medical Virology · doi:10.1002/jmv.1890260310 · Cited by 180 · see citing works

11β-Hydroxysteroid Dehydrogenase Type 1 Is Induced in Human Monocytes upon Differentiation to Macrophages

Thieringer, R., LeGrand, C. B., Carbin, L., Cai, T., Wong, B., Wright, S. D., & Hermanowski‐Vosatka, A. (2001) · The Journal of Immunology · doi:10.4049/jimmunol.167.1.30 · Cited by 177 · see citing works

Infection in Hospitalized Trauma Patients: Incidence, Risk Factors, and Complications

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24-Hour Secretory Pattern of Dehydroisoandrosterone and Dehydroisoandrosterone Sulfate

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Increased number of circulating Leu 11+ (CD 16) large granular lymphocytes and decreased NK activity during human ageing.

Facchini, A., Mariani, E., Mariani, A. R., Papa, S., Vitale, M., & Manzoli, F. A. (1987) · PubMed Central · Cited by 170 · see citing works

Dehydroepiandrosterone treatment of women with mild‐to‐moderate systemic lupus erythematosus: A multicenter randomized, double‐blind, placebo‐controlled trial

Chang, D., Lan, J., Lin, H., & Luo, S. (2002) · Arthritis & Rheumatism · doi:10.1002/art.10615 · Cited by 164 · see citing works

Raised cortisol:DHEAS ratios in the elderly after injury: potential impact upon neutrophil function and immunity

Butcher, S. K., Killampalli, V. V., Lascelles, D., Wang, K., Alpar, E. K., & Lord, J. M. (2005) · Aging Cell · doi:10.1111/j.1474-9726.2005.00178.x · Cited by 162 · see citing works

Activation of Immune Function by Dehydroepiandrosterone (DHEA) in Age-Advanced Men

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Biotransformation of Oral Dehydroepiandrosterone in Elderly Men: Significant Increase in Circulating Estrogens

Arlt, W., Haas, J., Callies, F., Reincke, M., Hübler, D., Oettel, M., Ernst, M. E., Schulte, H. M., & Allolio, B. (1999) · The Journal of Clinical Endocrinology & Metabolism · doi:10.1210/jcem.84.6.5789 · Cited by 158 · see citing works

An open study of dehydroepiandrosterone in systemic lupus erythematosus

van Vollenhoven, R., Engleman, E. G., & McGuire, J. L. (1994) · Arthritis & Rheumatism · doi:10.1002/art.1780370906 · Cited by 157 · see citing works

The Actions of Exogenous Dehydroepiandrosterone in Experimental Animals and Humans

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Stress responses and innate immunity: aging as a contributory factor

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Aging Alters Zonation in the Adrenal Cortex of Men

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Effects of prasterone on disease activity and symptoms in women with active systemic lupus erythematosus

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Conversion of dehydroepiandrosterone to downstream steroid hormones in macrophages

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Androstenediol and dehydroepiandrosterone protect mice against lethal bacterial infections and lipopolysaccharide toxicity

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Estradiol binding to cell surface raises cytosolic free calcium in T cells

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In vitro potentiation of lymphocyte activation by dehydroepiandrosterone, androstenediol, and androstenetriol.

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Serial estimation of interleukin 6 as a measure of systemic disease in rheumatoid arthritis.

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Immune response to influenza vaccination of elderly people. A randomized double-blind placebo-controlled trial

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Dehydroepiandrosterone stimulates nitric oxide release in vascular endothelial cells: evidence for a cell surface receptor

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Dehydroepiandrosterone protects mice from endotoxin toxicity and reduces tumor necrosis factor production

Danenberg, H. D., Alpert, G., Lustig, S., & Ben‐Nathan, D. (1992) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.36.10.2275 · Cited by 129 · see citing works

Reversal of the Immunosenescent Phenotype by Dehydroepiandrosterone: Hormone Treatment Provides an Adjuvant Effect on the Immunization of Aged Mice with Recombinant Hepatitis B Surface Antigen

Araneo, B. A., Woods, M. L., & Daynes, R. A. (1993) · The Journal of Infectious Diseases · doi:10.1093/infdis/167.4.830 · Cited by 123 · see citing works

Protection from glucocorticoid induced thymic involution by dehydroepiandrosterone

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Association of humoral markers of inflammation and dehydroepiandrosterone sulfate or cortisol serum levels in patients with chronic inflammatory bowel disease

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Dehydroepiandrosterone metabolism

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Dehydroepiandrosterone

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Administration of Dehydroepiandrosterone Suppresses Experimental Allergic Encephalomyelitis in SJL/J Mice

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The Expression of 11β-Hydroxysteroid Dehydrogenase Type I by Lymphocytes Provides a Novel Means for Intracrine Regulation of Glucocorticoid Activities

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Hormonal and pregnancy relationships to rheumatoid arthritis: Convergent effects with immunologic and microvascular systems

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Adrenal Hormone Modulation of Type 1 and Type 2 Cytokine Production by Spleen Cells: Dexamethasone and Dehydroepiandrosterone Suppress Interleukin-2, Interleukin-4, and Interferon-γ Productionin Vitro

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Dehydroepiandrosterone Stimulates Endothelial Proliferation and Angiogenesis through Extracellular Signal-Regulated Kinase 1/2-Mediated Mechanisms

Liu, D., Iruthayanathan, M., Homan, L. L., Wang, Y., Yang, L., Wang, Y., & Dillon, J. S. (2007) · Endocrinology · doi:10.1210/en.2007-1125 · Cited by 90 · see citing works

Dehydroepiandrosterone functions as more than an antiglucocorticoid in preserving immunocompetence after thermal injury

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Dehydroepiandrosterone inhibits the amplification of glucocorticoid action in adipose tissue

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Up-regulation of high-affinity dehydroepiandrosterone binding activity by dehydroepiandrosterone in activated human T lymphocytes

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Hepatocarcinogenicity of dehydroepiandrosterone in the rat.

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Dysregulation of IL-10 production with aging: Possible linkage to the age-associated decline in DHEA and its sulfated derivative

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Metabolism of Dehydroepiandrosterone

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DEHYDROEPIANDROSTERONE RESTORES IMMUNE FUNCTION FOLLOWING TRAUMA-HAEMORRHAGE BY A DIRECT EFFECT ON T LYMPHOCYTES

Catania, R. A., Angele, M. K., Ayala, A., Cioffi, W. G., Bland, K. I., & Chaudry, I. H. (1999) · Cytokine · doi:10.1006/cyto.1998.0458 · Cited by 85 · see citing works

Low serum levels of dehydroepiandrosterone may cause deficient IL-2 production by lymphocytes in patients with systemic lupus erythematosus (SLE)

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Dehydroepiandrosterone decreases mortality rate and improves cellular immune function during polymicrobial sepsis

Oberbeck, R., Dahlweid, M., Koch, R., van Griensven, M., Emmendörffer, A., Tscherne, H., & Pape, H. (2001) · Critical Care Medicine · doi:10.1097/00003246-200102000-00029 · Cited by 82 · see citing works

Dehydroepiandrosterone modulation of lipopolysaccharide-stimulated monocyte cytotoxicity

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Dehydroepiandrosterone 7α-hydroxylation in human tissues: Possible interference with type 1 11β-hydroxysteroid dehydrogenase-mediated processes

Hennebert, O., Chalbot, S., Alran, S., & Morfin, R. (2007) · The Journal of Steroid Biochemistry and Molecular Biology · doi:10.1016/j.jsbmb.2007.03.026 · Cited by 79 · see citing works

Dehydroepiandrosterone (DHEA) treatment reverses the impaired immune response of old mice to influenza vaccination and protects from influenza infection

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Androstenediol regulates systemic resistance against lethal infections in mice

Loria, R. M., & Padgett, D. A. (1992) · Archives of Virology · doi:10.1007/bf01309578 · Cited by 79 · see citing works

Inter-conversion of 7α- and 7β-hydroxy-dehydroepiandrosterone by the human 11β-hydroxysteroid dehydrogenase type 1

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Administration of Dehydroepiandrosterone to Burned Mice Preserves Normal Immunologic Competence

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Immune up-regulation and tumor apoptosis by androstene steroids

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DHEA Induces 11β-HSD2 by Acting on CCAAT/Enhancer-Binding Proteins

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Expression of 11β-hydroxysteroid dehydrogenase type 1 permits regulation of glucocorticoid bioavailability by human dendritic cells

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Prevention of immune dysfunction and vitamin E loss by dehydroepiandrosterone and melatonin supplementation during murine retrovirus infection

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Low blood and synovial fluid levels of sulpho-conjugated steroids in rheumatoid arthritis.

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Dehydroepiandrosterone Sulfate Enhances Natural Killer Cell Cytotoxicity in Humans Via Locally Generated Immunoreactive Insulin-Like Growth Factor I1

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Characteristics of the hepatocarcinogenesis caused by dehydroepiandrosterone, a peroxisome proliferator, in male F-344 rats

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Immunological studies of aging. IX. Impaired proliferation of T lymphocytes detected in elderly humans by flow cytometry.

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