The specific features of cellular immunity in pregnant women with systemic lupus erythematosus and their newborn infants


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

Subjects and methods. This prospective study enrolled 34 pregnant women with grade I-IIISLE and their neonates (a study group). The women took cytostatics and corticosteroids during pregnancy. A control group consisted of 21 women with the physiological course of pregnancy and labor, without autoimmune diseases, as well as their neonates. The count of main lymphocyte subpopulations and that of regulatory T cells CD4 +CD25 hlghCD127 low/ ) were measured in the maternal peripheral blood obtained at the end of the third trimester before labor and in the neonatal umbilical cord blood. The lymphocytes were phenotyped by flow cytometry using fluorescently labeled monoclonal antibodies to differentiated lymphocyte antigens. Results. There were considerable changes in the subpopulation composition of peripheral blood lymphocytes in pregnant women with SLE, which manifested themselves as an increase in the count of activated T lymphocytes (CD3 +HLA-DR +) and regulatory T cells (CD4 +CD25 hlgl/CD127 low/ ) and a decrease in that of natural cytotoxic cells (CD56/16 +). There were no significant differences in the subpopulation composition of neonatal umbilical cord blood lymphocytes in the study and control groups. Conclusion. During pregnancy, the cellular bases of fetal adaptive immunity may normally form and develop in pregnant women with SLE running during therapy with glucocorticosteroids and cytostatics.

Full Text

Restricted Access

About the authors

N. K Matveeva

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia

Email: matveeva_nk@mail.ru
candidate of biological science, senior researcher of clinical immunology laboratory

L. V Vanko

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia

Email: lvanko@mail.ru
MD, professor, leading research worker of clinical immunology laboratory

E. V Fedorova

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia

Email: KatrinaFedorova7@gmail.com
postgraduate of the 1st obstetric pregnancy pathology department

A. S Belyaeva

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia

Email: skazka_morozko@mail.ru
junior research worker of clinical immunology laboratory

N. I Klimenchenko

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia

Email: natalite@list.ru
PhD, head of the 1st obstetric pregnancy pathology department

M. A Nikolaeva

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia

Email: nikolaeva_ma@mail.ru
doctor of biological science, leading researcher of clinical immunology laboratory

V. G Safronova

Institute of Cell Biophysics, Russian Academy of Sciences

Email: safronova@icb.psn.ru
candidate of biological science, head of cellular neurobiology laboratory, Institute of Cell Biophysics

N. M Kosheleva

Academician V.A. Nasonova Research Institute of Rheumatology, Russian Academy of Medical Sciences

Email: nadkosheleva@yandex.ru
PhD, senior researcher of the 4th rheumatologic department

L. V Krechetova

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia

Email: k_l_v_@mail.ru
hD, head of clinical immunology laboratory

G. T Sukhikh

Academician V.I. Kulakov Research Center of Obstetrics, Gynecology and Perinatology, Ministry of Health of Russia

Email: g_sukhikh@oparina4.ru
MD, professor

References

  1. Насонов Е.Л., Насонова В.А., ред. Ревматология. Национальное руководство. М.: ГЭОТАР-Медиа; 2010. 720 с. [Nasonov E.L., Nasonova V.A., eds. Rheumatology. National Guide. M.: GEOTAR-Media; 2010. 720 p. (In Russian)]
  2. Созина А.В., Неустроева Ю.А., Тихомирова Т.А., Лапин С.В. Сочетанная встречаемость аутоантител у больных с диффузными болезнями соединительной ткани. Медицинская иммунология. 2007; 9(1): 69-76. [Sozina A.V., Neustroeva YU.A., Tihomirova T.A., Lapin S.V. Combined incidence of autoantibodies in patients with diffuse connective tissue disease. Meditsinskaya immunologiya. 2007; 9(1): 69-76. (In Russian)]
  3. Suen J.L., Chiang B.L. CD4(+)FoxP3(+) regulatory T-cells in human systemic lupus erythematosus. J. Formos. Med. Assoc. 2012; 111(9): 465-70.
  4. Gualtierotti R., Biggioggero M., Penatti A.E., Meroni P.L. Updating on the pathogenesis of systemic lupus erythematosus. Autoimmun. Rev. 2010; 10(1): 3-7.
  5. Dörner T., Jacobi A.M., Lee J., Lipsky P.E. Abnormalities of B cell subsets in patients with systemic lupus erythematosus. J. Immunol. Methods. 2011; 363(2): 187-97.
  6. Odendahl M., Jacobi A., Hansen A., Feist E., Hiepe F., Burmester G.R. et al. Disturbed peripheral B lymphocyte homeostasis in systemic lupus erythematosus. J. Immunol. 2000; 165(10): 5970-9.
  7. Jacobi A.M., Mei H., Hoyer B.F., Mumtaz I.M., Thiele K., Radbruch A. et al. HLA-DRhigh/CD27high plasmablasts indicate active disease in patients with systemic lupus erythematosus. Ann. Rheum. Dis. 2010; 69(1): 305-8.
  8. Jacobi A.M., Reiter K., Mackay M., Aranow C., Hiepe F., Radbruch A. et al. Activated memory B cell subsets correlate with disease activity in systemic lupus erythematosus: delineation by expression of CD27, IgD, and CD95. Arthritis Rheum. 2008; 58(6): 1762-73.
  9. Iikuni N., Lourenço E. V., Hahn B.H., La Cava A. Cutting edge: regulatory T cells directly suppress B cells in systemic lupus erythematosus. J. Immunol. 2009; 183(3): 1518-22.
  10. Crispin J.C., Martinez A., Alcocer-Varela J. Quantification of regulatory T cells in patients with systemic lupus erythematosus. J. Autoimmun. 2003; 21: 273-6.
  11. Liu M.F., Wang C.R., Fung L.L., Wu C.R. Decreased CD4+CD25+ T cells in peripheral blood of patients with systemic lupus erythematosus. Scand. J. Immunol. 2004; 59: 198-202.
  12. Fathy A., Mohamed R.W., Tawfik G.A., Omar A.S. Diminished CD4+CD25+ T-lymphocytes in peripheral blood of patients with systemic lupus erythematosus. Egypt. J. Immunol. 2005; 12: 25-31.
  13. Zhang B., Zhang X., Tang F., Zhu L., Liu Y. Reduction of forkhead box P3 levels in CD4+CD25high T cells in patients with new-onset systemic lupus erythematosus. Clin. Exp. Immunol. 2008; 153(2): 182-7.
  14. Doria A., Iaccarino L., Sarzi-Puttini P., Ghirardello A., Zampieri S., Arienti S. et al. Estrogens in pregnancy and systemic lupus erythematosus. Ann. N.Y. Acad. Sci. 2006; 1069: 247-56.
  15. Grant C.H. Progesterone and autoimmune disease. Autoimmun. Rev. 2012; 11(6-7): A502-14.
  16. Doria A., Tincani A., Lockshin M. Challenges of lupus pregnancies. Rheumatology. 2008; 47(Suppl. 3): iii9-12.
  17. Somerset D.A., Zheng Y., Kilby M.D., Sansom D.M., Drayson M.T. Normal human pregnancy is associated with an elevation in the immune suppressive CD25+ CD4+ regulatory T-cell subset. Immunology. 2004; 112(1): 38-43.
  18. Toldi G., Saito S., Shima T., Haimos A., Veresh Z., Vásárhelyi B., Rigó J., Molvarec A. The frequency of peripheral blood CD4+ CD25high FoxP3+ and CD4+ CD25- FoxP3+ regulatory T cells in normal pregnancy and pre-eclampsia. Am. J. Reprod. Immunol. 2012; 68(2): 175-80.
  19. Федорова Е.В., Матвеева Н.К., Ванько Л.В., Клименченко Н.И., Беляева А.С., Кошелева Н.М., Матьянова Е.В., Сухих Г.Т. Клинико-иммунологическая характеристика беременных женщин с системной красной волчанкой. Акушерство и гинекология. 2013; 12: 46-51. [Fedorova E.V., Matveeva N.K., Vanko L.V., Klimenchenko N.I., Belyaeva A.S., Kosheleva N.M., Matyanova E.V., Sukhikh G.T. Clinical and immunological characteristics of pregnant women with systemic lupus erythematosus. Akusherstvo i ginekologiya/ Obstetrics and Gynecology. 2013; 12: 46-51. (In Russian)]
  20. Seddiki N., Santner-Nanan B., Martinson J., Zaunders J., Sasson S., Landay A. et al. Expression of interleukin (IL)-2 and IL-7 receptors discriminates between human regulatory and activated T cells. J. Exp. Med. 2006; 203(7): 1693-700.
  21. Alvarado-Sanchez B., Hernandez-Castro B., Portales-Perez B., Baranda L., Layseca-Espinosa E., Abud-Mendoza C. et al. Regulatory T cells in patients with systemic lupus erythematosus. J. Autoimmun. 2006; 27: 110-8.
  22. Venigalla R.K., Tretter Ch., Krienke T.S., Max R., Eckstein V., Blank N. et al. Reduced CD4+, CD25- T cell sensitivity to the suppressive function of CD4+, CD25high,CD127 -/low regulatory T cells in patients with active systemic lupus erythematosus. Arthritis Rheum. 2008; 58(7): 2120-30.
  23. Motta M., Ciardelli L., Marconi M., Tincani A., Gasparoni A., Lojacono A., Chirico G. Immune system development in infants born to mothers with autoimmune disease, exposed in utero to immunosuppressive agents. Am. J. Perinatol. 2007; 24(8): 441-7.

Supplementary files

Supplementary Files
Action
1. JATS XML

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies