IMPAIRED IMMUNE MECHANISMS DUE TO PERINATAL STRESS: EXPERIMENTAL AND CLINICAL FINDINGS


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Abstract

The stress reaction becomes a nonspecific cause of many pathological conditions in which the impaired immune protection mechanisms are of fundamental importance. Objective. To analyze the data available in the literature on studies of immune disorders due to the prenatal stress experienced.ц Subject and methods. The key words, such stress, glucocorticoids, immunity, adrenals, were used to search for data in international and Russian databases. A total of 39 sources on suitable themes were selected. Results. The mechanisms of adaptive responses are interlinked in a complex manner and may be multidirectional with the possibility of changing from protective to destructive ones. They become a basis for the development of pathological processes that depend on the number, intensity, and duration of stress factors and on the specific features of the body and its predisposition to different pathological processes. Conclusion. Impaired immune protection mechanisms are of prime importance in the development of these complications.

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About the authors

Anna Drastamatovna Khudaverdyan

Yerevan State Medical University

Email: anna.khudaverdyan2@mail.ru
MD, PhD, senior lecturer, Department of Obstetrics and Gynecology #2 Armenia, Yerevan 0025, Koryun str. 2

Adelina Levanovna Torgomyan

Yerevan State Medical University

MD, PhD, senior lecturer, Department of Physiology Armenia, Yerevan 0025, Koryun str. 2

Drastamat Nagapetovich Khudaverdyan

Yerevan State Medical University

MD, PhD, professor Head of Physiology department Armenia, Yerevan 0025, Koryun str. 2

References

  1. Петров Р.В. Иммунология и иммуногенетика. М.; 1976. 414с.
  2. Checkley S. Neuroendocrine mechanisms and the precipitation of depression by life events. Br. J. Psychiatry. 1992; 160(15, Suppl.): 7-17.
  3. Glaser R., Kiecolt-Glaser J.K. Stress-induced immune dysfunction: implications for health. Nat. Rev. Immunol. 2005; 5(3): 243-51.
  4. Glaser R., MacCallum R.C., Laskowski B.F., Malarkey W.B., Sheridan J.F., Kiecolt-Glaser J.K. Evidence for a shift in the Th-1 to Th-2 cytokine response associated with chronic stress and aging. J. Gerontol. A Biol. Sci. Med. Sci. 2001; 56(8): M477-82.
  5. Elenkov I.J., Chrousos G.P. Stress hormones, Th1/Th2 patterns, Pro/Antiinflammatory cytokines and susceptibility to disease. Trends Endocrinol. Metab. 1999; 10(9): 359-68.
  6. Elenkov I.J. Glucocorticoids and the Th1/Th2 balance. Ann. N. Y. Acad. Sci. 2004; 1024: 138-46.
  7. Segerstrom S.C., Miller G.E. Psychological stress and the human immune system: a meta-analytic study of 30 years of inquiry. Psychol. Bull. 2004; 130(4): 601-30.
  8. Stefanski V., Raabe C., Schulte M. Pregnancy and social stress in female rats: influences on blood leukocytes and corticosterone concentrations. J. Neuroimmunol. 2005; 162(1-2): 81-8.
  9. Kay G., Tarcic N., Poltyrev T., Weinstock M. Prenatal stress depresses immune function in rats. Physiol. Behav. 1998; 63(3): 397-402.
  10. Klein S.L., Rager D.R. Prenatal stress alters immune function in the offspring of rats. Dev. Psychobiol. 1995; 28(6): 321-36.
  11. Reul J.M., Stec I., Wiegers G.J., Labeur M.S., Linthorst A.C., Arzt E., Holsboer F. Prenatal immune challenge alters the hypothalamic-pituitary-adrenocortical axis in adult rats. J. Clin. Invest. 1994; 93(6): 2600-7.
  12. Llorente E., Brito M.L., Machado P., Gonzalez M.C. Effect of prenatal stress on the hormonal response to acute and chronic stress and on immune parameters in the offspring. J. Physiol. Biochem. 2002; 58(3): 143-9.
  13. Entringer S., Epel E.S., Kumsta R., Lin J., Hellhammer D.H., Blackburn E.H. et al. Stress exposure in intrauterine life is associated with shorter telomere length in young adulthood. Proc. Natl. Acad. Sci. USA. 2011; 108(33): E513-8.
  14. Hodyl N.A., Krivanek K.M., Lawrence E., Clifton V.L., Hodgson D.M. Prenatal exposure to a pro-inflammatory stimulus causes delays in the development of the innate immune response to LPS in the offspring. J. Neuroimmunol. 2007; 190(1-2): 61-71.
  15. Götz A.A., Wittlinger S., Stefanski V. Maternal social stress during pregnancy alters immune function and immune cell numbers in adult male Long-Evans rat offspring during stressful life-events. J. Neuroimmunol. 2007;185(1-2): 95-102.
  16. Götz A.A., Wolf M., Stefanski V. Psychosocial maternal stress during pregnancy: effects on reproduction for F0 and F1 generation laboratory rats. Physiol. Behav. 2008; 93(4-5): 1055-60.
  17. Vanbesien-Mailliot C.C., Wolowczuk I., Mairesse J., Viltart O., Delacre M., Khalife J. et al. Prenatal stress has pro-inflammatory consequences on the immune system in adult rats. Psychoneuroendocrinology. 2007; 32(2): 114-24.
  18. Reul J.M., Stec I., Wiegers G.J., Labeur M.S., Linthorst A.C., Arzt E., Holsboer F. Prenatal immune challenge alters the hypothalamic-pituitary-adrenocortical axis in adult rats. J. Clin. Invest. 1994; 93(6): 2600-7.
  19. Pincus-Knackstedt M.K., Joachim R.A., Blois S.M., Douglas A.J., Orsal A.S., Klapp B.F. et al. Prenatal stress enhances susceptibility of murine adult offspring toward airway inflammation. J. Immunol. 2006; 177(12): 8484-92.
  20. Couret D., Jamin A., Kuntz-Simon G., Prunier A., Merlot E. Maternal stress during late gestation has moderate but long-lasting effects on the immune system of the piglets. Vet. Immunol. Immunopathol. 2009; 131(1-2): 17-24.
  21. Couret D., Prunier A., Mounier A.M., Thomas F., Oswald I.P., Merlot E. Comparative effects of a prenatal stress occurring during early or late gestation on pig immune response. Physiol. Behav. 2009; 98(4): 498-504.
  22. Tuchscherer M., Kanitz E., Otten W., Tuchscherer A. Effects of prenatal stress on cellular and humoral immune responses in neonatal pigs. Vet. Immunol. Immunopathol. 2002; 86(3-4): 195-203.
  23. Coe C.L., Crispen H.R. Social stress in pregnant squirrel monkeys (Saimiri boliviensis peruviensis) differentially affects placental transfer of maternal antibody to male and female infants. Health Psychol. 2000; 19(6): 554-9.
  24. Coe C.L., Kramer M., Kirschbaum C., Netter P., Fuchs E. Prenatal stress diminishes the cytokine response of leukocytes to endotoxin stimulation in juvenile rhesus monkeys. J. Clin. Endocrinol. Metab. 2002; 87(2): 675-81.
  25. Coe C.L., Lubach G.R., Karaszewski J.W. Prenatal stress and immune recognition of self and nonself in the primate neonate. Biol. Neonate. 1999; 76(5): 301-10.
  26. Coe C.L., Lubach G.R. Prenatal origins of individual variation in behavior and immunity. Neurosci. Biobehav. Rev. 2005; 29(1): 39-49.
  27. Wright R.J., Visness C.M., Calatroni A., Grayson M.H., Gold D.R., Sandel M.T. et al. Prenatal maternal stress and cord blood innate and adaptive cytokine responses in an inner-city cohort. Am. J. Respir. Crit. Care Med. 2010; 182(1): 25-33.
  28. Entringer S., Epel E.S., Kumsta R., Lin J., Hellhammer D.H., Blackburn E.H. et al. Stress exposure in intrauterine life is associated with shorter telomere length in young adulthood. Proc. Natl. Acad. Sci. USA. 2011; 108(33): E513-8.
  29. Entringer S., Kumsta R., Nelson E.L., Hellhammer D.H., Wadhwa P.D., Wüst S. Influence of prenatal psychosocial stress on cytokine production in adult women. Dev. Psychobiol. 2008; 50(6): 579-87.
  30. Mosmann T.R., Sad S. The expanding universe of T-cell subsets: Th1, Th2 and more. Immunol. Today. 1996; 17(3): 138-46.
  31. Marshall G.D. Jr.,Agarwal S.K., Lloyd C., Cohen L., Henninger E.M., Morris G.J. Cytokine dysregulation associated with exam stress in healthy medical students. Brain Behav. Immun. 1998; 12(4): 297-307.
  32. Wadhwa P.D. Psychoneuroendocrine processes in human pregnancy influence fetal development and health. Psychoneuroendocrinology. 2005; 30(8): 724-43.
  33. Wadhwa P.D. Prenatal stress and life-span development. In: Friedman H.S., ed. Encyclopedia of mental health. San Diego: Academic Press; 1998; vol.3: 265-80.
  34. Sawyer R., Hendrickx A., Osburn B., Terrell T., Anderson J. Abnormal morphology of the fetal monkey (Macaca mulatta) thymus exposed to a corticosteroid. J. Med. Primatol. 1977; 6(3): 145-50.
  35. Knackstedt M.K., Hamelmann E., Arck P.C. Mothers in stress: consequences for the offspring. Am. J. Reprod. Immunol. 2005; 54(2): 63-9.
  36. Prescott S.L., Macaubas C., Smallacombe T., Holt B.J., Sly P.D., Holt P.G. Development of allergen specific T-cell memory in atopic and normal children. Lancet. 1999; 353(9148): 196-200.
  37. Coussons-Read M.E., Okun M.L., Nettles C.D. Psychosocial stress increases inflammatory markers and alters cytokine production across pregnancy. Brain Behav. Immun. 2007; 21(3): 343-50.
  38. Munck A., Guyre P.M., Holbrook N.J. Physiological functions of glucocorticoids in stress and their relation to pharmacological actions. Endocr. Rev. 1984; 5(1): 25-44.
  39. Holsboer F. The hypothalamic-pituitary-adrenocorticalsystem.In: Paykel E.S., ed. Handbook of affective disorders. Edinburgh: Churchill Livingstone; 1992; 267-87

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