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"Child`s Health" Том 12, №7, 2017

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Development of the immune response in pneumonia due to Staphylococcus aureus (part 6)

Authors: Абатуров А.Е., Никулина А.А.
ГУ «Днепропетровская медицинская академия МЗ Украины», г. Днепр, Украина

Categories: Pediatrics/Neonatology

Sections: Specialist manual

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Summary

У статті на підставі літературних даних продемонстрована роль клітинних реакцій у розвитку імунної відповіді при пневмонії, спричиненої Staphylococcus aureus. Описані механізми взаємодії Staphylococcus aureus з тучними клітинами, нейтрофілами і дендритними клітинами респіраторного тракту. Надана порівняльна характеристика нейтрофільного та макрофагального фагоцитозу.

В статье на основании литературных данных продемонстрирована роль клеточных реакций в развитии иммунного ответа при пневмонии, вызванной Staphylococcus aureus. Описаны механизмы взаимодействия Staphylococcus aureus с тучными клетками, нейтрофилами и дендритными клетками респираторного тракта. Дана сравнительная характеристика нейтрофильного и макрофагального фагоцитоза.

The article on the basis of literature data demonstrates the role of cellular reactions in the development of the immune response in pneumonia caused by Staphylococcus aureus. Тhe mechanisms of interaction of Staphylococcus aureus with mast cells, neutrophils and dendritic cells of the respiratory tract are described. A comparative cha­racteristics of neutrophilic and macrophagal phagocytosis is given.


Keywords

пневмонія; Staphylococcus aureus; фагоцитоз; нейтрофіли

пневмония; Staphylococcus aureus; фагоцитоз; нейтрофилы

pneumonia; Staphylococcus aureus; phagocytosis; neutrophils


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Bibliography

1. Aleyd E. IgA enhances NETosis and release of neutrophil extracellular traps by polymorphonuclear cells via Fcα receptor I / E. Aleyd, M.W. van Hout, S.H. Ganzevles et al. // J. Immunol. — 2014, Mar 1. — 192(5). — 2374-83. — doi: 10.4049/jimmunol.1300261.
2. Bekeredjian-Ding I. Plasmacytoid Dendritic Cells: Neglected Regulators of the Immune R esponse to Staphylococcus aureus / I. Beke–redjian-Ding, J. Greil, S. Ammann, M. Parcina // Front. Immunol. — 2014, May 23. — 5. — 238. — doi: 10.3389/fimmu.2014.00238. 
3. Bekeredjian-Ding I., Stein C., Uebele J. The Innate Immune Response Against Staphylococcus aureus // Curr. Top. Microbiol. Immunol. — 2015, Dec 15. — doi: 10.1007/82_2015_5004.
4. Bratton D.L., Henson P.M. Neutrophil clearance: when the party is over, clean-up begins // Trends Immunol. — 2011 Aug. — 32(8). — 350-7. — doi: 10.1016/j.it.2011.04.009.
5. Cui F., Meng J., Luo P, Chen P. IFN- alpha blocks IL-17 production by peripheral blood mononuclear cells in patients with chronic active hepatitis B Infection // BMC Infect. Dis. — 2014, Feb 1. — 14. — 55. — doi: 10.1186/1471-2334-14-55.
6. DeLeo F.R., Nauseef W.M. Granulocytic phagocytes // Bennet J.E., Dolin R., Blaser M.J., editors. Mandell, Douglas, and Bennett’s principles and practice of infectious diseases. 
8. This textbook chapter is a comprehensive review of the cell and molecular biology of human neutrophils. — Philadelphia, PA: Elsevier/Saunders, 2014.
7. Delgado-Rizo V. Neutrophil Extracellular Traps and Its Implications in Inflammation: An Overview / V. Delgado-Rizo, M.A. Martínez-Guzmán, L. Iñiguez-Gutierrez et al. // Front. Immunol. — 2017, Feb 6. — 8. — 81. — doi: 10.3389/fimmu.2017.00081.
8. Frodermann V. A modulatory interleukin-10 response to staphylo–coccal peptidoglycan prevents Th1/Th17 adaptive immunity to Staphylococcus aureus / V. Frodermann, T.A. Chau, S. Sayedyahossein et al. // J. Infect. Dis. — 2011, Jul 15. — 204(2). — 253-62. — doi: 10.1093/infdis/jir276.
9. Greenlee-Wacker M., DeLeo F.R., Nauseef WM. How methicillin-resistant Staphylococcus aureus evade neutrophil killing // Curr. Opin. Hematol. — 2015 Jan. — 22(1). — 30-5. — doi: 10.1097/MOH.0000000000000096.
10. Greenlee-Wacker M.C. Clearance of apoptotic neutrophils and resolution of inflammation // Immunol. Rev. — 2016 Sep. — 273(1). — 357-70. — doi: 10.1111/imr.12453.
11. Guilliams M. Dendritic cells, monocytes and macrophages: a unified nomenclature based on ontogeny / M. Guilliams, F. Ginhoux, C. Jakubzick et al. // Nat. Rev. Immunol. — 2014 Aug. — 14(8). — 571-8. — doi: 10.1038/nri3712.
12. Günther F. Host defence against Staphylococcus aureus biofilms infection: phagocytosis of biofilms by polymorphonuclear neutrophils (PMN) / F. Günther, G.H. Wabnitz, P. Stroh et al. // Mol. Immunol. — 2009 May. — 46(8–9). — 1805-13. — doi: 10.1016/j.molimm.2009.01.020.
13. Honda T. Neutrophil left shift and white blood cell count as markers of bacterial infection / T. Honda, T. Uehara, G. Matsumoto, S. Arai, M. Sugano // Clin. Chim. Acta. — 2016, Jun 1. — 457. — 46-53. — doi: 10.1016/j.cca.2016.03.017.
14. Hong S.J. Wall teichoic acid is an essential component of Staphylococcus aureus for the induction of human dendritic cell maturation / S.J. Hong, S.K. Kim, E.B. Ko et al. // Mol. Immunol. — 2017 Jan. — 81. — 135-142. — doi: 10.1016/j.molimm.2016.12.008.
15. Jin J.O. BDCA1-positive dendritic cells (DCs) represent a unique human myeloid DC subset that induces innate and adaptive immune responses to Staphylococcus aureus Infection / J.O. Jin, W. Zhang, J.Y. Du, Q. Yu // Infect. Immun. — 2014 Nov. — 82(11). — 4466-76. — doi: 10.1128/IAI.01851-14.
16. Kamenyeva O. Neutrophil recruitment to lymph nodes limits local humoral response to Staphylococcus aureus / O. Kamenyeva, C. Boularan, J. Kabat et al. // PLoS Pathog. — 2015, Apr 17. — 11(4). — 1004827. — doi: 10.1371/journal.ppat.1004827.
17. Kolaczkowska E., Kubes P. Neutrophil recruitment and function in health and inflammation // Nat. Rev. Immunol. — 2013 Mar. — 13(3). — 159-75. — doi: 10.1038/nri3399.
18. Kurokawa K., Takahashi K., Lee B.L. The staphylococcal surface-glycopolymer wall teichoic acid (WTA) is crucial for complement activation and immunological defense against Staphylococcus aureus infection // Immunobiology. — 2016 Oct. — 221(10). — 1091-101. — doi: 10.1016/j.imbio.2016.06.003. 
19. Lund L.D., Ingmer H., Frøkiær H. D-Alanylation of Teichoic Acids and Loss of Poly-N-Acetyl Glucosamine in Staphylococcus aureus during Exponential Growth Phase Enhance IL-12 Production in Murine Dendritic Cells // PLoS One. — 2016, Feb 12. — 11(2). — 0149092. — doi: 10.1371/journal.pone.0149092.
20. McGuinness W.A., Kobayashi S.D., DeLeo F.R. Evasion of Neutrophil Killing by Staphylococcus aureus // Pathogens. — 2016, Mar 17. — 5(1). — 32. — doi: 10.3390/pathogens5010032.
21. Michea P. Epithelial control of the human pDC response to extracellular bacteria / P. Michea, P. Vargas, M.H. Donnadieu et al. // Eur. J. Immunol. — 2013 May. — 43(5). — 1264-73. — doi: 10. 1002/eji.201242990.
22. Navegantes K.C. Immune modulation of some autoimmune diseases: the critical role of macrophages and neutrophils in the innate and adaptive immunity / K.C. Navegantes, R. de Souza Gomes, P.A. Pereira et al. // J. Transl. Med. — 2017, Feb 15. — 15(1). — 36. — doi: 10.1186/s12967-017-1141-8.
23. Nguyen Q.T. Role of Interleukin-12 in Protection against Pulmonary Infection with Methicillin-Resistant Staphylococcus aureus / Q.T. Nguyen, Y. Furuya, S. Roberts, D.W. Metzger // Antimicrob. Agents Chemother. — 2015 Oct. — 59(10). — 6308-16. — doi: 10.1128/AAC.00968-15.
24. Nordenfelt P., Tapper H. Phagosome dynamics during phagocytosis by neutrophils // J. Leukoc. Biol. — 2011 Aug. — 90(2). — 271-84. — doi: 10.1189/jlb.0810457.
25. Parcina M. Pathogen-triggered activation of plasmacytoid dendritic cells induces IL-10-producing B cells in response to Staphylococcus aureus / M. Parcina, M.A. Miranda-Garcia, S. Durlanik et al. // J. Immunol. — 2013, Feb 15. — 190(4). — 1591-602. — doi: 10.4049/jimmunol.1201222. 
26. Parker D. Innate Immune Signaling Activated by MDR Bacteria in the Airway / D. Parker, D. Ahn, T. Cohen, A. Prince // Physiol. Rev. — 2016 Jan. — 96(1). — 19-53. — doi: 10.1152/physrev.00009.2015.
27. Patel V.I., Metcalf J.P. Identification and characterization of human dendritic cell subsets in the steady state: a review of our current knowledge // J. Investig. Med. — 2016 Apr. — 64(4). — 833-47. — doi: 10.1136/jim-2016-000072.
28. Pilsczek F.H. A novel mechanism of rapid nuclear neutrophil extracellular trap formation in response to Staphylococcus aureus / F.H. Pilsczek, D. Salina, K.K. Poon et al. // J. Immunol. — 2010, Dec 15. — 185(12). — 7413-25. — doi: 10.4049/jimmunol.1000675.
29. Puga I. B cell-helper neutrophils stimulate the diversification and production of immunoglobulin in the marginal zone of the spleen / I. Puga, M. Cols, C.M. Barra et al. // Nat. Immunol. — 2011, Dec 25. — 13(2). — 170-80. — doi: 10.1038/ni.2194.
30. Rankin S.M. The bone marrow: a site of neutrophil clea–rance // J. Leukoc. Biol. — 2010 Aug. — 88(2). — 241-51. — doi: 10.1189/jlb.0210112.
31. Rigby K.M., DeLeo F.R. Neutrophils in innate host defense against Staphylococcus aureus infections // Semin. Immunopathol. — 2012 Mar. — 34(2). — 237-59. — doi: 10.1007/s00281-011-0295-3.
32. Robertson C.M. Neutrophil depletion causes a fatal defect in murine pulmonary Staphylococcus aureus clearance / C.M. Robertson, E.E. Perrone, K.W. McConnell et al. // J. Surg. Res. — 2008 Dec. — 150(2). — 278-85. — doi: 10.1016/j.jss.2008.02.009.
33. Rönnberg E. Mast cells are activated by Staphylococcus aureus in vitro but do not influence the outcome of intraperitoneal S. aureus infection in vivo / E. Rönnberg, C.F. Johnzon, G. Calounova et al. // Immunology. — 2014 Oct. — 143(2). — 155-63. — doi: 10.1111/imm.12297.
34. Roquilly A. CpG-ODN and MPLA prevent mortality in a murine model of post-hemorrhage-Staphyloccocus aureus pneumonia / A. Roquilly, L. Gautreau, J.P. Segain et al. // PLoS One. — 2010, Oct 7. — 5(10). — 13228. — doi: 10.1371/journal.pone.0013228.
35. Sadik C.D., Kim N.D., Luster A.D. Neutrophils casca–ding their way to inflammation // Trends Immunol. — 2011 Oct. — 32(10). — 452-60. — doi: 10.1016/j.it.2011.06.008.
36. Scapini P. Human neutrophils in the saga of cellular heterogeneity: insights and open questions / P. Scapini, O. Marini, C. Tecchio, M.A. Cassatella // Immunol. Rev. — 2016 Sep. — 273(1). — 48-60. — doi: 10.1111/imr.12448.
37. Schindler D. Dendritic cells are central coordinators of the host immune response to Staphylococcus aureus bloodstream infection / D. Schindler, M.G. Gutierrez, A. Beineke et al. // Am. J. Pathol. — 2012 Oct. — 181(4). — 1327-37. — doi: 10.1016/j.ajpath.2012.06.039.
38. Selders G.S. An overview of the role of neutrophils in innate immunity, inflammation and host-biomaterial integration / G.S. Selders, A.E. Fetz, M.Z. Radic, G.L. Bowlin // Regen. Biomater. — 2017 Feb. — 4(1). — 55-68. — doi: 10.1093/rb/rbw041.
39. Spaan A.N. Neutrophils versus Staphylococcus aureus: a biological tug of war / A.N. Spaan, B.G. Surewaard, R. Nijland, J.A. van Strijp // Ann. Rev. Microbiol. — 2013. — 67. — 629-50. — doi: 10.1146/annurev-micro-092412-155746.
40. Strydom N., Rankin S.M. Regulation of circulating neutrophil numbers under homeostasis and in disease // J. Innate Immun. — 2013. — 5(4). — 304-14. — doi: 10.1159/000350282.
41. Swiecki M., Colonna M. The multifaceted biology of plasmacytoid dendritic cells // Nat. Rev. Immunol. — 2015 Aug. — 15(8). — 471-85. — doi: 10.1038/nri3865.
42. Thammavongsa V. Staphylococcal manipulation of host immune responses / V. Thammavongsa, H.K. Kim, D. Missiakas, O. Schneewind // Nat. Rev. Microbiol. — 2015 Sep. — 13(9). — 529-43. — doi: 10.1038/nrmicro3521.
43. Thurlow L.R. Staphylococcus aureus biofilms prevent macrophage phagocytosis and attenuate inflammation in vivo / L.R. Thurlow, M.L. Hanke, T. Fritz et al. // J. Immunol. — 2011, Jun 1. — 186(11). — 6585-96. — doi: 10.4049/jimmunol.1002794.
44. Tong S.Y. Staphylococcus aureus infections: epidemio–logy, pathophysiology, clinical manifestations, and management / S.Y. Tong, J.S. Davis, E. Eichenberger et al. // Clin. Microbiol. Rev. — 2015 Jul. — 28(3). — 603-61. — doi: 10.1128/CMR.00134-14.
45. Tsuda Y. Three different neutrophil subsets exhibited in mice with different susceptibilities to infection by methicillin-resistant Staphy–lococcus aureus / Y. Tsuda, H. Takahashi, M. Kobayashi et al. // Immunity. — 2004 Aug. — 21(2). — 215-26. — doi: 10.1016/j.immuni.2004.07.006.
46. van Kessel K.P., Bestebroer J., van Strijp J.A. Neutrophil-Mediated Phagocytosis of Staphylococcus aureus // Front. Immunol. — 2014, Sep 26. — 5. — 467. — doi: 10.3389/fimmu.2014.00467. 
47. Waters E.M. Convergence of Staphylococcus aureus Persister and Biofilm Research: Can Biofilms Be Defined as Communities of Adherent Persister Cells? / E.M. Waters, S.E. Rowe, J.P. O’Gara, B.P. Conlon // PLoS Pathog. — 2016, Dec 29. — 12(12). — 1006012. — doi: 10.1371/journal.ppat.1006012.
48. Worbs T. Dendritic cell migration in health and disease / T. Worbs, S.I. Hammerschmidt, R. Förster et al. // Nat. Rev. Immunol. — 2017 Jan. — 17(1). — 30-48. — doi: 10.1038/nri.2016.116.
49. Wu X., Xu F. Dendritic cells during Staphylococcus aureus infection: subsets and roles // J. Transl. Med. — 2014, Dec 18. — 12. — 358. — doi: 10.1186/s12967-014-0358-z.
50. Yang F. The Diverse Biological Functions of Neutrophils, Beyond the Defense Against Infections / F. Yang, C. Feng, X. Zhang, J. Lu, Y. Zhao // Inflammation. — 2017 Feb. — 40(1). — 311-323. — doi: 10.1007/s10753-016-0458-4.

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