Kuyun L. O.

DIFFERENCES AND DYSFUNCTIONS IN SYSTEMIC AND LOCAL IMMUNE RESPONCES IN COPD PATIENTS


About the author:

Kuyun L. O.

Heading:

CLINICAL AND EXPERIMENTAL MEDICINE

Type of article:

Scentific article

Annotation:

Objective: to study differences and dysfunctions in systemic and local immune responses in COPD patients; develop a specific method for prophylaxis and treatment of this disease. Methods and materials. Materials used in the research were obtained from 50 COPD patients during the exacerbation stage. There were 48 healthy individuals in the control group. Analysis of the serum levels of immunoglobulins (Ig) A, M, and G was conducted using an immunoturbidimetric method. The population and subpopulations of the immune cells were identified using an immunofluorescence flow cytometry method. The same method was used to evaluate phagocytic activity of monocytes in the peripheral blood. The data obtained during the research was statistically processed. Results and their discussion. Analysis of materials taken from 50 COPD patients during the exacerbation stage showed changes in content of their immune cells in the peripheral blood compared to the data obtained from the specimens taken from 48 people in the control group. A significant increase of the percentage ratio was observed in CD3+ CD8+ (Т cytotoxic lymphocytes) and СD3+ CD8+ HLA-DR active Т cytotoxic lymphocytes in COPD patients compared to the ratio of these subpopulations in the control group, p<0,001. The number of NK cells in patients decreased significantly compared to the data obtained from the control group, p<0,001. The author’s immunohistochemical study of morphological changes in terminal bronchioles in COPD patients showed high numbers of goblet cells, small clusters of lung macrophages and relatively small peribronchial fibrosis. The immunohistochemical analysis of the immune cells in the peripheral blood of COPD patients was somewhat different from that obtained from the morphological analysis of lung tissue in terminal bronchioles. Chronic inflammation during COPD at the local level is realized through intensive migration of CD3+ Т-lymphocytes, Т-helpers CD3+ CD4 + and cytotoxic CD3+ CD8+ Т-cells into the wall of its own plate of terminal bronchioles. Alveolar macrophages in COPD patients are characterized by a phagocytosis defect, which leads to multiple exacerbations in patients with COPD. Immunoglobulin A serum levels increased significantly in COPD patients when compared to the control group, p<0,001.

Tags:

COPD, analysis of peripheral blood cells, local and systemic immune response, alveolar and interstitial macrophages, blood monocytes.

Bibliography:

  1. Kapellos TS, Bassler K, Aschenbrenner AC, Fujii W, Schultze JL. Dysregulated Functions of Lung Macrophage Populations in COPD. J. Immunol. Res. 2018 Feb;18:2349045.
  2.  Schyns J, Bureau F, Marichal T. Lung Interstitial Macrophages: Past, Present, and Future. J. Immunol. Res. 2018 Apr;30:5160794.
  3. Wang Y, Xu J, Meng Y, Adcock IM, Yao X. Role of inflammatory cells in airway remodeling in COPD. Int. J. Chron. Obstruct. Pulmon. Dis. 2018;13:3341-8.
  4. Singh D, Agusti A, Anzueto A, Barnes PJ, Bourbeau J, Celli BR, et al. Global Strategy for the Diagnosis, Management, and Prevention of Chronic Obstructive Lung Disease: the GOLD science committee report 2019. Eur. Respir. J. 2019 May;18:53(5).
  5. Villani AC, Satija R, Reynolds G, Sarkizova S, Shekhar K, Fletcher J, et al. Single-cell RNA-seq reveals new types of human blood dendritic cells, monocytes, and progenitors. Science. 2017 Apr 21;356(6335).
  6. Saetta M, Di Stefano A, Maestrelli P, Ferraresso A, Drigo R, Potena A, et al. Activated T-lymphocytes and macrophages in bronchial mucosa of subjects with chronic bronchitis. Am. Rev. Respir. Dis. 1993 Feb;147(2):301-6.
  7. Lundborg M, Dahlen SE, Johard U, Gerde P, Jarstrand C, Camner P. Aggregates of ultrafine particles impair phagocytosis of microorganisms by human alveolar macrophages. Environ. Res. 2006 Feb;100(2):197-204.
  8. Di Stefano A, Capelli A, Lusuardi M, Balbo P, Vecchio C, Maestrelli P, et al. Severity of airflow limitation is associated with severity of airway inflammation in smokers. Am. J. Respir. Crit. Care Med. 1998 Oct;158(4):1277-85.
  9. Dang X, Qu X, Wang W, Liao C, Li Y, Zhang X, et al. Bioinformatic analysis of microRNA and mRNA Regulation in peripheral blood mononuclear cells of patients with chronic obstructive pulmonary disease. Respir Res. 2017;18:4.
  10. Yang SR, Chida AS, Bauter MR, Shafiq N, Seweryniak K, Maggirwar SB, et al. Cigarette smoke induces proinflammatory cytokine release by activation of NF- kB and posttranslational modifications of histone deacetylase in macrophages. Am. J. Physiol. Lung Cell Mol. Physiol. 2006 Jul;291(1):L46-57.
  11. Sethi S, Evans N, Grant BJ, Murphy TF. New strains of bacteria and exacerbations of chronic obstructive pulmonary disease. N. Engl. J. Med. 2002 Aug 15;347(7):465-71.
  12. Chauhan S, Gupta MK, Goyal A, Dasgupta DJ. Alterations in immunoglobulin & complement levels in chronic obstructive pulmonary disease. Indian J. Med. Res. 1990 Aug;92:241-5.
  13. Wortham BW, Eppert BL, Motz GT, Flury GL, Orozco-Levi M, Hoebe K. NKG2D Mediates NK Cell Hyperresponsiveness and Influenza-Induced Pathologies in a Mouse Model of Chronic Obstructive Pulmonary Disease. J. Immunol. 2012 May 1;188(9):4468-75.
  14. Tschernig T, Rabung A, Voss M, Meier C, Bals R, Beisswenger C. Chronic inhalation of cigarette smoke reduces phagocytosis in peripheral blood leukocytes. BMC Res. Notes. 2015;8:705.

Publication of the article:

«Bulletin of problems biology and medicine» Issue 2 Part 1 (150), 2019 year, 144-147 pages, index UDK 616.24-007.271-036.12-097

DOI: