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The impact of Immunomodulators on Reactivity the immune System cells in Model Vaccinal process against Tularemia

https://doi.org/10.31631/2073-3046-2016-15-3-94-101

Abstract

Investigated is the effect of azoximer bromide (polioxidonium - PO) and dalargin (DA) on the immune system cell reactivity in the anti-tularemia vaccine prosess modeling in Balb/c mice. The animals were immunized subcutaneously with a dose of 104 live microbial cells of vaccine strain Francisella tularensis 15 NIIEG. PO or DA subcutaneously administered 60 min before vaccination, respectively, in doses of 4 mg and 2 mg. On 3rd and 21st days of immunogenesis the peripheral organs of the immune system and the contents of the abdominal cavity were investigated. Cell response to vaccination and investigated immunomodulators evaluated by flow cytometry (CyAn ADP) for two light scatter parameters and for changing the proliferating and apoptotic cell number. Additionally, for the characterization of changes in the functional status of lymphocytes nuclei the light microscopy was used and titers of specific antibodies were determined. Installed is the different response of intact mice lymphocytes and phagocytes to PO and DA introduction. As distinct from PO, DA stimulated the lymphocete proliferation and macrophage apoptosis by acting on their cytoplasmic granules. PO activated the migration of phagocytes with high cytoplasmic granules from mice abdominal cavity in the spleen. Only when using the PO as an immunomodulator in anti-tularemia vaccine process modeling recorded a significant increase in specific antibody titers against the background of a long-term functional splenocyte activation and macrophages reduced macrophage damage intensity in the spleen and abdomen.

About the Authors

A. L. Kravtsov
Federal State institution of public Health «Russian Scientific Research Institute «Microbe» Federal Service for Surveillance on consumer Rights Protection and Human Wellbeing
Russian Federation


S. N. Klyueva
Federal State institution of public Health «Russian Scientific Research Institute «Microbe» Federal Service for Surveillance on consumer Rights Protection and Human Wellbeing
Russian Federation


S. A. Bugorkova
Federal State institution of public Health «Russian Scientific Research Institute «Microbe» Federal Service for Surveillance on consumer Rights Protection and Human Wellbeing
Russian Federation


References

1. Sayapina L.V., Solov,ev E.A., Goryaev A.A., Bondarev V.P. Studies of of immunological properties in Francisella tularensis vaccine strain 15 NIIEG under extended storage conditions. Problems particularly dangerous infections. 2015; 2: 87 – 91 (in Russian).

2. Karalnik B.V., Ponomareva T.S., Deryabin P.N., Denisova T.G., Mel,nikova N.N., Tugambaev T.I. The impact of immunomodulation on immunogenic and protective activity of alive plague. Zhurnal mikrobiol., epidemiol. i immunobiol.2014; 6: 108 – 112 (in Russian).

3. Klyueva S.N., Schukovskaya T.N. Effect of a new generation of adjuvants in vitro cytokine production by blood cells of vaccinated individuals against plague. Russian Immunological Journal. 2015; 9 (2): 201 – 208 (in Russian).

4. Ljapina A.M., Poljanina T.I., Ul’janova O.V., Eliseev Ju.Ju., Telepnev M.V., Motin V.L., Fedorova V.A. Application polioksidonija to produce specific antibodies to bacterial antigens. Modern problems of science and education. 2012. № 2. http: www.science-education.ru/102-5729 (in Russian).

5. Kiseleva E.P. New concepts of anti-infective immunity. Infection and Immunity. 2011; 1: 9 – 14 (in Russian).

6. Silva M.T. When two is better than one: macrophages and neutrophils work in concert in innate immunity as complementary and cooperative partners of a myeloid phagocyte system. J. Leukocyte Biology. 2010; 87: 1 – 14.

7. Pham C.T. Neutrophil serine proteases fine-tune the inflammatory response. Int. J. Biochem. Cell Biol. 2008; 40 (6 – 7): 1317 – 1333.

8. Pinegin B.V., Nekrasov A.V., Haitov R.M. Immunomodulator polyoxidonium: mechanisms of action and aspects of clinical application. Cytokines and inflammation. 2004; 3: 41 – 47 (in Russian).

9. Balachevskiy B.V., Kurzanov A.N., Slavinskiy A.A. Dalargin-induced modulation of the functional-metabolic activity of neutrophils. The success of modern science. 2008; 5: 75 – 77 (in Russian).

10. Silva T.M., do Vale A., dos Santos N.M. Secondary necrosis in multicellular animals: an outcome of apoptosis with pathogenic implications. Apoptosis. 2008; 13: 463 – 482.

11. Mares C.A., Ojeda S.S., Morris E.G., Li Q., Teale J.M. Initial delay in the immune response to Francisella tularensis is followed by hypercytokinemia characteristic of severe sepsis and correlating with upregulation and release of demage-associated molecular patterns. Infec. Immunity.2008; 76: 3001 – 3010.

12. Frimel X. Immunological methods. Moscow. Medicine; 1987: 472 (in Russian).

13. Sibiryak S.V., Khaidukov S.V., Zurochka A.V. Evaluation of apoptosis in immunological research. Clinical application. Chelyabinsk. Paper Yard; 2008:195 (in Russian).

14. Bi Y., Du Z., Yang H. Guo Z., Tan Y., Zhu Z., Yang R. Reduced apoptosis of mouse macrophages induced by yscW mutant of Yersinia pestis results from the reduced secretion of YopJ and relates to caspase-3 signal pathway. Scand. J. Immunol. 2009; 70 (4):358 – 367.

15. Iritani B.M., Eisenman R.N. C-Myc enhances protein synthesis and cell size during B lymphocyte development. PNAS. 1999; 96(23): 13180 – 13185.

16. Sklar L.A., Oades Z.G., Finnay D.A. Neutrophil degranulation detected by right angle light scattering: spectroscopic methods suitable for simultaneous analysis of degranulation or shape change, elastase realease, and cell aggregation. J. Immunology. 1984; 133 (3): 1483 – 1487.

17. Korzhevskij D.Je., Giljarov A.V. Basics of histologic techniques. St. Petersburg: Ltd. Publishing SpetsLit; 201: 96 (in Russian).

18. Howell W.M., Black D.A. Controlled silver staining of nucleolus organizer regions with a protective colloidal developer: a one-step method. Experientia. 1980; 36: 1014 – 1015.

19. Bugorkova S.A., Schukovskaja T.N., Kurylina A.F. Nucleolar apparatus of lymphocytes - as an indicator of the functional activity of lymphoid organs in the preclinical evaluation of vaccines. Problems particularly dangerous infections. 2015; 2: 75 – 78 (in Russian).

20. Kombarova T.I. Selection algorithm and preliminary evaluation of candidates for vaccine strains of tularemia microbe. Doctorate of biol. sci. diss. Obolensk; 2013 (in Russian).

21. Houghton A.M., Hartzell W.O., Robbins C.S., Gomis-Rüth F.X., Shapiro S.D. Macrophage elastase kills bacteria within murine macrophages. Nature Letters. 2009; 460: 637 – 642.

22. Steen H.B., Boye E. Escherichia coli growth studied by dual parameter flow cytophotometry. J. Bacteriology. 1981; 145 (2): 1091 – 1094.

23. Marohn M.E., Barry E.M. Live attenuated tularemia vaccines: recent developments and future goals. Vaccine. 2013; 2; 31(35):3485 – 3491. doi: 10.1016/j.

24. Firstova V.V., Pavlov V.M., Gorbatov A.A., Kombarova T.I., Karaulov A.V., Dyatlov I.A. The development of cellular and humoral immune responses, induced in mice by Francisella tularensis 15 NIIEG. Immunology. 2014; 35 (3): 147 – 150 (in Russian).


Review

For citations:


Kravtsov A.L., Klyueva S.N., Bugorkova S.A. The impact of Immunomodulators on Reactivity the immune System cells in Model Vaccinal process against Tularemia. Epidemiology and Vaccinal Prevention. 2016;15(3):94-101. (In Russ.) https://doi.org/10.31631/2073-3046-2016-15-3-94-101

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ISSN 2073-3046 (Print)
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