DETERMINATION OF FcγRIIIb (CD16) EXPRESSION ON THE SURFACE OF BLOOD NEUTROPHILS IN ANTI-PLAGUE VACCINATED PEOPLE

DOI: https://doi.org/10.29296/24999490-2020-02-06

A.L. Kravtsov , S.A. Bugorkova, S.N. Klyueva, V.A. Kozhevnikov, O.M. Kudryavtseva Russian Research Anti-Plague Institute «Microbe», Universitetskaya str, 46, Saratov, 410005, Russian Federation E-mail: [email protected]

Aim. Comparative evaluation of FcγRIIIb (CD16) expression level on the surface of blood neutrophils in vaccinated and unvaccinated people before and after the interaction of сells in vitro with the plague microbe allergen (pestin). Materials and methods. Blood samples of 25 healthy donors not vaccinated against the plague were examined, as well as 40 volunteers who were vaccinated once and several times with the plague vaccine alive, before and during different periods (1, 6 months) after the vaccination. The expression of CD16 on the surface of neutrophil granulocytes was determined by flow cytometry before and after incubation of blood samples for 4 hours with pestin. Results. After vaccination in all subjects there was registered a significant increase in the expression level of the CD16 molecule on the surface of blood neutrophils. After in vitro contact with pestin, the expression level of the FcγRIIIb molecule (CD16) decreased on the surface of neutrophils only in blood samples of people vaccinated against the plague. Conclusion. The change in the neutrophil phenotype from CD16bright to CD16dim, revealed by in vitro interaction with blood pestin grafted against the plague of people, mimics the response of these cells in anaphylactic shock mediating with specific IgG, and apparently represent the result of the functioning of the FcγRIIIb (CD16) as a trigger for netosis.
Keywords: 
FcγRIIIb (CD16) expression, flow cytometry, anti-plague vaccination

Список литературы: 
  1. Nesterova I.V., Kolesnikova N.V., Chudilova G.A., Lomtatidze L.V., Kovaleva S.V., Evglevskij A.A. Nejtrofil'nye granulotsity: novyj vzgljad na «staryh igrokov» na immunologicheskom pole. Immunologija. 2015; 36 (4): 257–65. [Nesterova I.V., Kolesnikova N.V., Chudilova G.A., Lomtatidze L.V., Kovaleva S.V., Evglevskii A.A. Neutrophilic granulocytes: a new look at «old players» on the immunological field. Im- munologiya. 2015; 36 (4): 257–65 (in Russian)]
  2. Eisele N., Lee-Lewis H., Besch-Williford C., Brown C.R., Anderson D.M. Chemokine receptor CXCR2 mediates bacterial clear- ance rather than neutrophil recruitment in a murine model of pneumonic plague. Am. J. Pathol. 2011; 178 (3): 1190–200. https://doi.org/10.1016/j.ajpath.2010.11.067.
  3. MsDonald B., Urrutia R., Yipp B.G., Jenne C.N., Kubes P. Intravascular neutrophil extracellular traps capture bacteria from bloodstream during sepsis. Cell Host Microbe. 2012; 12 (3): 324–33. https://doi. org/10.1016/j.chom.2012.06.011.
  4. Aleman O.R., Mora N., Cortes-Vieyra R., Uribe-Querol E., Rosales C. Differential use of human Fcγ-receptors for inducing neutrophil extracellular traps formation. J. Immunology Research. 2016; 17 pages, ID 2908034, http:// dx.doi.org./10.1155/2016/2908034.
  5. Williams T.E., Nagavajan S., Selvaraj P., Zhu C. Concurrent and independent binding of Fcγ receptors IIa and IIIb to surface-bound IgG. Biophysical J. 2000; 79 (4): 1867–75.
  6. Elghetany M.T. Surface antigen changes during normal neutrophilic development: a critical review. Blood Cell. Mol. Dis. 2002; 28: 260–74.
  7. Nesterova I.V., Chudilova G.A., Lom- tatidze L.V., Kovaleva S.V., Kolesni- kova N.V., Avdeeva M.G., Rusinova E.V. Differentsirovannost' variantov subpopuljatsij transformirovannogo fenotipa CD16+CD11b+ nejtrofil'nyh granulotsitov pri ostroj virusnoj i ostroj bakterial'noj infektsijah. Immu- nologija. 2016; 37 (4): 199–204. https://doi. org/10.18821/0206-4952-2016-37-4-199-204. [Nesterova I.V., Chudilova G.A., Lomtatidze L.V., Kovaleva S.V., Kolesnikova N.V., Avdeeva M.G., Rusinova E.V. Differentiationof variants subpopulations transformed phenotype CD16+CD11b+ neutrophils in acute viral and acute bacterial infec- tions. Immunologiya 2016; 37 (4): 199–204. https://doi.org/10.18821/0206-4952-2016- 37-4-199-204 (in Russian)]
  8. Dudte S.C., Hinnebusch B.J., Shannon J.G. Characterization of Yersinia pestis interactions with human neutrophils in vitro. Front Cell Infect. Microbiology. 2017; 7: 358. https://doi.org/10.3389/fcimb.2017.00358.
  9. Landoni V.I., Chiarella P., Martire-Greco D., Schierloh P., van-Rooijen N., Rearte B., Palermo M.S., Isturiz M.A., Fernandez G.C. Tol- erance to lipopolysaccharide promotes an enhanced neutrophil extracellular traps for- mation leading to a more efficient bacterial clearance in mice. Clinical and Experimental Immunology. 2012; 168: 153–63. https://doi. org/10.1111/j.1365-2249.2012.04560.x.
  10. Fradkin V.A. Diagnostika allergii reaktsijami nejtrofilov krovi. M.: Me- ditsina, 1985; 176. [Fradkin V.A. Diagnostic of allergy by blood neutrophil reactions. M.: Medicina, 1985; 176 (in Russian)]
  11. Korobkova E.I. Kozhnaja allergicheskaja reaktsija kak pokazatel' immuniteta pri chume. Zhurnal mikrobiologii, epidemi- ologii i immunobiologii. 1955; 4: 40–7. [Korobkova E.I. Skin allergic reaction as an indicator of immunity in plague. Zhurnal mikrobiologii, epidemiologii i immunobi- ologii 1955; 4: 40–7 (in Russian)]
  12. Bugorkova S.A., Schukovskaja T.N., Mikshis N.I., Kljueva S.N., Kudrjavtseva O.M., Kravtsov A.L., Goncharova A.Ju., Kozhevni- kov V.A., Sandzhiev D.N., Konusheva S.V., Savchenko S.P., Scherbakova S.A., Kutyrev V.V. Kompleksnoe immunologicheskoe issledovanie vaktsinirovannyh zhivoj chumnoj vaktsinoj lits, prozhivajuschih na territorii Prikaspijskogo peschanogo ochaga chumy v Respublike Kalmykija. Epidemiologija i vaktsinoprofilak- tika. 2018; 17 (3): 38–50. https://doi. org/10.31631/2073-3046-2018-17-3-38-50. [Bugorkova S. A., Shchukovskaya T. N., Mikshis N. I., Klyueva S.N., Kudryavtseva O.M., Kravtsov A.L., Goncharova A.Yu., Kozhevnikov V.A., Sandzhiev D.N., Konusheva S.V., Savchenko S.P., Shcherbakova S.A., Kutyrev V.V.Comprehensive immuno- logical study of persons vaccinated with live plague vaccine living on the territory of the Pre-Caspian sand foci of the plague in the republic of Kalmykia. Epidemiologiya i vaktsinoprofilaktika 2018; 17 (3): 38–50. https://doi.org/10.31631/2073-3046-2018- 17-3-38-50 (in Russian)]
  13. Tosi M.F., Berger M. Functional differences between the 40 kDa and 50 to 70 kDa IgG Fc-receptors on human neutrophils revealed by elastase treatment and anti- receptor antibodes. J. Immunology. 1988; 141 (6): 2097–103.
  14. Pham C.T. Neutrophil serine proteases fine-tune the inflammatory response. Int. J. Biochem. Cell Biol. 2008; 40 (6–7): 1317–33.
  15. Papayannopoulos V., Metzier K.D., Hakkim A., Zychlinsky A. Neutrophil elastase and myeloperoxidase regulate the formation of neutrophil extracellular traps. J. Cell Biol. 2010; 191: 677–91.
  16. Khodoun M.V., Strait R., Armstrong L., Yanase N., Finkelman F.D. Identification of markers that distinguish IgE- from IgG-mediated anaphylaxis. PNAS. 2011; 108 (30): 12413–8. https:/doi.org/10.1073/pnas. 1105695108.
  17. Branzk N., Lubojemska A.. Hardison S.E., Wang Q., Guttierrez M.G., Broun G.D., Papa- yannopoulos V. Neutrophil sense microbial size and selectively release neutrophil extra- cellular traps in response to large patho- gens. Nat. Immunol. 2014; 15 (11): 1017–25. https://doi.org/10.1038/ni.2987.
  18. Monteseirin J., Bonilla I., Camacho M.J., Chason P., Vega A., Chaparro A., Conde J., Sobrino F. Specific allergens enhance elastase release in stimulated neutrophils from asthmatic patients. Int. Arch. Allergy Immunology. 2003; 131 (3): 174–81.
  19. Kravtsov A.L., Shmel'kova T.P., Schukovskaja T.N. Vlijanie protivochumnoj vaktsinatsii na funktsional'nuju aktivnost' kletok vrozh- dennogo immuniteta cheloveka. Problemy osobo opasnyh infektsij. 2011; 107: 77–80. [Kravtsov A.L., Shmel’kova T.P., Shchukovs- kaya T.N. Effect of anti-plague vaccination on the functional activity of the human in- nate immune cells. Problemy osobo opas- nykh infektsii 2011; 107: 77–80