scholarly journals Formation of Cellular Responses in the Adaptive Immune Response of 40–60-Year-Old Women Living in Northern Russia

Author(s):  
Mohammad S. Kabbani ◽  
◽  
Oksana E. Filippova ◽  
Elizaveta Yu. Shashkova ◽  
Marina V. Men’shikova ◽  
...  

Sustainable development of Russian Arctic territories requires creating favourable living conditions and preserving public health. Living in high latitudes, one is exposed to adverse environmental factors, which can lead to changes in the activity of life functions, including the immune response. The study of the lymphoid population ratio allows us to reveal the age-related formation of the adaptive immune response in women born and living in the Russian North, which is especially important given the increasing retirement age. The purpose of this work was to determine the ratio of lymphoid populations in the adaptive immune response in women between the ages of 40 and 60 born and living in the North of the Russian Federation. Two groups of women – aged 40–49 and 50–60 years – living in the town of Nadym (Yamalo-Nenets Autonomous Okrug) and Pinega settlement (Arkhangelsk Region) were examined using the method of indirect immunoperoxidase reaction with monoclonal antibodies (Sorbent, Moscow). The analysis on the immune status included determining lymphocytes with CD3+ (mature lymphoid cells), CD4+ (T helper cells), CD8+ (cytotoxic T lymphocytes), CD16+ (natural killers), and HLA-DR+ (activated В cells with major histocompatibility complex class II receptors) markers in the peripheral blood. We found that the adaptive immune response is formed in 40–49-year-old women as a result of cell-mediated cytotoxic activity of the T-cell component (CD8+) in 68.0 % and due to natural killers (CD16+) in 72.0 % of cases; in women aged 50–60 years, as a result of a pronounced deficiency of mature and functionally active T cells (CD3+) in 96.3 %, low helper activity (CD4+) in 18.5 %, and decreased activation of lymphocytes with major histocompatibility complex class II receptors (HLA-DR+) reflecting B-cell activity in 25.9 % of cases.

1996 ◽  
Vol 134 (4) ◽  
pp. 449-453 ◽  
Author(s):  
Arthur B Parkes ◽  
Christopher Darke ◽  
Sakinah Othman ◽  
Melanie Thomas ◽  
Neil Young ◽  
...  

Parkes AB, Darke C, Othman S, Thomas M, Young N, Richards CJ, Hall R, Lazarus JH. Major histocompatibility complex class II and complement polymorphisms in postpartum thyroiditis. Eur J Endocrinol 1996;134:449–53. ISSN 0804–4643 The objective was to re-evaluate the association between class II HLA-DR and DQ MHC antigens and postpartum thyroiditis (PPT) and to determine the prevalence of the class III complement allotypes of Properdin factor B (Bf), C4A and C4B in this condition. Two hundred and sixty-five (of 2897) pregnant women screened positive for thyroid autoantibody activity took part. Further blood samples were obtained for HLA class II (185) and complement (193) typing. The severity of the ensuing PPT was assessed by measuring thyroid function during the postpartum year. The HLA-DR and DQ phenotypes were assigned from restriction fragment length polymorphism analysis, and Bf, C4A and C4B allotypes were determined by immunofixation with anti-Bf or anti-C4 antibodies after electrophoresis. A weak association between the HLA class II antigens and PPT, as indicated by a reduced frequency of DR15 and DQ6 together with an increased frequency of DR5 and DQ7. was confirmed. However, only the change in DR5 frequency remained significant after correction (corrected p < 0.05). Postpartum thyroiditis was also associated with frequency disturbances in Bf and C4A allotypes but not C4B allotypes. Whilst this study has not provided evidence of a strong marker gene for PPT, it does not preclude the involvement of the MHC in this condition. These data show disturbances in complement allotype frequencies, suggesting that the class III region may provide a useful focus for further study of this pathology. AB Parkes, Autoimmunology Research Unit, Section of Endocrinology, Metabolism and Diabetes, Department of Medicine, University of Wales College of Medicine, Heath Park, Cardiff CF4 4XN, UK


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