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Problems of Particularly Dangerous Infections

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Historical and Modern Views on the Problem of Specific Plague Prophylaxis

https://doi.org/10.21055/0370-1069-2013-3-63-69

Abstract

Objective of this review is to analyze diachronically paradigm shift as regards problems of specific plague prophylaxis and appreciate contribution of the present-day scientific discoveries in the sphere of plague agent investigations and peculiarities of its interaction with host organism to the solution of topical issues of vaccine development that will be safe and tangibly effective against this particularly dangerous disease. Outlined is the historical background of the conceptual evolution concerning specific plague prophylaxis and events that are landmarked with eminent scientific discoveries by A.Yersin, French researcher and microbiologist. Given are the data on the current state of plague immune-prophylaxis both in Russia and around the world. Through the prism of the latest researches that assume application of advanced technological resource of medical sciences (molecular biology, biotechnology, bioinformatics, molecular immunology) put forward is the prospective of search and construction of safe and effective anti-plague next generation vaccines.

About the Authors

S. A. Bugorkova
Russian Research Anti-Plague Institute “Microbe”
Russian Federation


Z. L. Devdariani
Russian Research Anti-Plague Institute “Microbe”
Russian Federation


T. N. Shchukovskaya
Russian Research Anti-Plague Institute “Microbe”
Russian Federation


V. V. Kutyrev
Russian Research Anti-Plague Institute “Microbe”
Russian Federation


References

1. Byvalov A.A., Evstigneev V.I., Darmov I.V., Pimenov E.M. [Antigen composition of plague chemical vaccine]. RF Patent 2190424.

2. Ganin V. [The war on “black death”: change from defense to offense]. Nauka i zhizn’. 2006; 7:17–24.

3. Dalvadyants S.M., Dubrovin M.Yu., Byvalov A.A., Dodonov N.P., Chicherin Yu.V., Evstigneev V.I., Pimenov E.V., Yeremin S.A, Dyatlov I.A, Kutyrev V.V. [A study of immunization against plague. Communication 3. Revaccination properties of the plague vaccine and the preparations of plague chemical vaccines for Hamadryas baboons]. Probl. Osobo Opasn. Infek. 2005; 89:62–7.

4. Dalvadyants S.M., Dyatlov I.A., Yeremin S.A., Schukovskaya T.N., Sayapina L.V., Sergheyeva G.M., Kutyrev V.V. [Plague immunization studies. Communication 4. An experience of volunteer revaccination with the “chemical” and live plague vaccines]. Probl. Osobo Opasn. Infek. 2006; 91:57–61.

5. Darmov I.V., Pogorel’sky I.P., Ezhov A.V., Mokhov D.A., Khonin A.Z. [Studies of immunobiological properties of a EV P2 Y. pestis-based dry live plague vaccine]. In: [Scientific Works Devoted to the 75th Anniversary of the Research Institute of Microbiology of the RF Ministry of Defense]. Kirov; 2003. P. 77.

6. Evstigneev V.I., Abdullin T.G. [Contribution of the Research Institute of Microbiology (the RF Ministry of Defense) to the development of the system providing for biological protection of RF military forces and population]. In: [Diagnostics, Treatment, and Prophylaxis of Infectious Diseases. Biotechnology. Veterinary]. Kirov, 1988. P. 3–10.

7. Korobkova E.I. [Live Anti-Plague Vaccine]. M.: Medgiz; 1956. 206 p.

8. Kutyrev V.V., Eroshenko G.A., Kukleva L.M., Shavina N.Yu., Vinogradova N.A. [Comparative genetic characteristics of the vaccine strain Yersinia pestis EV and its proposed ”virulent derivates”]. Zh. Mikrobiol. Epidemiol. Immunobiol. 2009; 3:50–6.

9. Lebedev K.A., Ponyakina I.D. [Immunology of Pattern Recognition Receptor (Integral Immunology)]. M.: “LIBROKOM”; 2009. 256 p.

10. Supotnitsky M.V., Supotnitskaya N.S. [Notes on the History of Plague]. M.: Vuzovskaya kniga; 2006. Vol. 1.468 p.

11. Airhart C.L., Rohde H.N., Hovde C.J., Bohach G.A., Deobald C.F., Lee S.S., Minnich S.A. Lipid A mimetics are potent adjuvants for an intranasal pneumonic plague vaccine. Vaccine. 2008; 26:5554–61.

12. Albrecht M.T., Eyles J.E., Baillie L.W., Keane-Myers A.M. Immunogenicity and efficacy of an anthrax/plague DNA fusion vaccine in a mouse model. FEMS Immunology & Medical Microbiology. 2012; 65(3):505–9.

13. Amedei A., Niccolai E., Marino L., D’Elios M. Role of immune response in Yersinia pestis infection. J. Infect. Dev. Ctries. 2011; 5(9):628–39.

14. Blisnick T., Ave P., Huerre M., Carniel E., Demeure C.E. Oral vaccination against bubonic plague using a live avirulent Yersinia pseudotuberculosis strain. Infect. Immun. 2008; 76(8):3808–16

15. Boyer J.L., Sofer-Podesta C., Ang J., Hackett N.R., Chiuchiolo M.J., Senina S., Perlin D., Crystal R.G. Protective immunity against a lethal respiratory Yersinia pestis challenge induced by V antigen or the F1 capsular antigen incorporated into adenovirus capsid. Hum Gene Ther. 2010; 21(7):891–901.

16. Branger C.G., Sun W., Torres-Escobar A., Perry R., Roland K.L., Fetherston J., Curtiss R., III. Evaluation of Psn, HmuR and a modified LcrV protein delivered to mice by live attenuated Salmonella as a vaccine against bubonic and pneumonic Yersinia pestis challenge. Vaccine. 2010; 29:274–82.

17. Caulfield A.J., Lathem W.W. Substrates of the plasminogen activator protease of Yersinia pestis. Adv. Exp. Med. Biol. 2012; 954:253–60.

18. Cooper A.M., Khader S. IL-12p40: an inherently agonistic cytokine. Trends Immunol. 2007; 28:33–8.

19. Covert B.A., Spencer J.S., Orme I.M., Belisle J.T. The application of proteomics in defining the T-cell antigens of Mycobacterium tuberculosis. Proteomic. 2001; 1(4):574–86.

20. Cowan C., Jones H.A., Kaya Y.H., Perry R.D., Straley S.C. Invasion of epithelial cells by Yersinia pestis: evidence for a Y. pestis-specific invasin. Infect Immun. 2000; 68(8):4523–30.

21. Dabbagh K., Dahl M.E., Stepick-Biek P., Lewis D.B. Toll-like receptor 4 is required for optimal development of Th2 immune responses: role of dendritic cells. J. Immunol. 2002; 168:4524–7.

22. Dziarski R. Innate immunity. Shaechter’s Mechanisms of Microbial Disease. 4th ed. Engelberg R., DiRita V., editors. Lippincott: Williams & Wilkins; 2006. P. 66–89.

23. Eisenbarth S.C., Piggott D.A., Huleatt J.W., Visintin I., Herrick C.A., Bottomly K. Lipopolysaccharide‐enhanced Toll‐like receptor 4-dependent T helper cell type 2 responses to inhaled antigen. J. Exp. Med. 2002; 196:1645–51.

24. Erova T.E., Rosenzweig J.A., Sha J., Suarez G., Sierra J.C., Kirtley M.L., van Lier C.S., Telepnev M.V., Motin V.L., Chopra A.K. Evaluation of protective potential of Yersinia pestis outer membrane protein antigens as possible candidates for a new-generation recombinant plague accine. Clin. Vaccine Immunol. 2013; 20(2):227–38.

25. Gelman A.E., Zhang J., Choi Y., Turka L.A. Toll-like receptor ligands directly promote activated CD4 T cell survival. J. Immunol. 2004; 172:6065–73.

26. Girard G., Robic J. Vaccination pesteuse par germs vivants (virus vaccine EV) Trois annees de l’application a Madagaskar. Bull. Acad. Med. 1938; 120:54–60.

27. Hines J., Skizypek E., Kajava A.V. Structure-function analysis of Yersinia pestis YopM’s interaction with α-thrombin to rule on its significance in systemic plague and to model YopM’s mechanism of binding host proteins. Microb. Pathog. 2001; 30(4):193–209.

28. Jones A., Bosio C., Duffy A., Goodyear A., Schriefer M., Dow S. Protection against pneumonic plague following oral immunization with a nonreplicating vaccine. Vaccine. 2010; 28:5924–9.

29. Khader S., Partida-Sanchez S., Bell G., Jelley-Gibbs D., Swain S., Pearl J., Ghilardi N., Desauvage F., Lund F., Cooper A. Interleukin 12p40 is required for dendritic cell migration and T cell priming after Mycobacterium tuberculosis infection. J. Exp. Med. 2006; 203:1805–15.

30. Kumar D., Kirimanjeswara G., Metzger D.W. Intranasal administration of an inactivated Yersinia pestis vaccine with interleukin-12 generates protective immunity against pneumonic plague. Clin. Vaccine Immunol. 2010; 18(11):1925–35.

31. Lahteemaki K., Kukkonen M., Korhonen T.K. Pia surface protease/adhesin of Yersinia pestis mediates bacterial invasion into human endothelial cells. FEMS Lett. 2001; 504(7):69–72.

32. Li B., Yang R. Interaction between Yersinia pestis and the host immune system. Infect. Immun. 2008; 76(5):1804–11.

33. Mellado-Sanchez G., Ramirez K., Drachenberg C.B., Diaz-McNair J., Rodriguez A.L., Galen J.E., Nataro J.P., Pasetti M.F. Characterization of systemic and pneumonic murine models of plague infection using a conditionally virulent strain. Comp. Immun. Microbiol. Infect. Dis. 2013; 36:113–28.

34. Montminy S.W., Khan N., McGrath S., Walkowicz M.J., Sharp F., Conlon J.E., Fukase K., Kusumoto S., Sweet C., Miyake K., Akira S., Cotter R.J., Goguen J.D., Lien E. Virulence factors of Yersinia pestis are overcome by a strong lipopolysaccharide response. Nat. Immunol. 2006; 7(10):1066–73.

35. Navarro L., Alto N.M., Dixon J.E. Functions of the Yersinia effector proteins in inhibiting host immune responses. Curr. Opin. Microbiol. 2005; 8(1):21–7.

36. Parent M.A., Berggren K.N,. Kummer L.W., Wilhelm L.B., Szaba F.M., Mullarky I.K., Smiley S.T. Cell-mediated protection againstpulmonary Yersinia pestis infection. Infect. Immun. 2005; 73:7304–10.

37. Parent M.A., Wilhelm L.B., Kummer L.W., Szaba F.M., Mullarky I.K., Smiley S.T. Gamma interferon, tumor necrosis factor alpha, and nitric oxide synthase 2, key elements of cellular immunity, perform critical protective functions during humoral defense against lethal pulmonary Yersinia pestis infection. Infect. Immun. 2006; 74:3381–6.

38. Quenee L.E., Hermanas T.M., Ciletti N., Louvel H., Miller N.C., Elli D., Blaylock B., Mitchell A., Schroeder J., Krausz T., Kanabrocki J., Schneewind O. Hereditary hemochromatosis restores the virulence of plague vaccine strains. J. Infect. Dis. 2012; 7:1050–58.

39. Reisner B.S., Straley S.C. Yersinia pestis YopM: thrombin binding and overexpression. Infect. Immun. 1992; 60:5242–52.

40. Robinson W.H. Antigen arrays for antibody profiling. Curr. Opin. Chem. Biol. 2006; 10(1):67–72.

41. Robinson R.T., Khader S.A., Locksley R.M., Lien E., Smiley S.T.,Cooper A.M. Yersinia pestis evades TLR4-dependent induction of IL-12(p40)2 by dendritic cells and subsequent cell migration. J. Immunol. 2008; 181:5560–7.

42. Sebbane F., Jarrett C.O., Gardner D., Long D., Hinnebusch B.J. Role of the Yersinia pestis plasminogen activator in the incidence of distinct septicemic and bubonic forms of flea-borne plague. Proc. Natl. Acad. Sci. USA. 2006; 103:5526–30.

43. Spinner J.L., Cundiff J.A., Kobayashi S.D. Yersinia pestis type III secretion system-dependent inhibition of human polymorphonuclear leukocyte function. Infect Immun. 2008; 76(8): 3754–60.

44. Sun W., Roland K.L., Kuang X., Branger C.G., Curtiss R. III. Yersinia pestis with regulated delayed attenuation as a vaccine candidate to induce protective immunity against plague. Infect. Immun. 2010; 78:1304–13.

45. Sun W., Roland K.L., Curtiss R. 3rd. Developing live vaccines against Yersinia pestis. J. Infect. Dev. Ctries. 2011; 5:614–27.

46. Telepnev M.V., Klimpel G.R., Haithcoat J., Knirel Y.A., Anisimov A.P., Motin V.L. Tetraacylated lipopolysaccharide of Yersinia pestis can inhibit multiple Toll-like receptor-mediated signaling pathways in human dendritic cells. J. Infect. Dis. 2009; 200:1694–702.

47. Viboud G.I., Bliska J.B. Yersinia outer proteins: role in modulation of host cell signaling responses and pathogenesis. Annu Rev. Microbiol. 2005; 59:69–89.

48. Wang Z., Zhou L., Qi Z., Zhang Q., Dai R., Yang Y., Cui B., Wang H., Yang R., Wang X. Long-term observation of subunit vaccine F1-rV270 against Yersinia pestis in mice. Clin. Vaccine Immunol. 2010; 17(1):199–201.

49. Zauberman A., Cohen S., Mamroud E., Flashner Y., Tidhar A., Ber R., Elhanany E., Shafferman A., Velan B. Interaction of Yersinia pestis with macrophages: limitations in YopJ-dependent apoptosis. Infect. Immun. 2006; 74(6):3239–50.

50. Zauberman A., Tidhar A., Levy Y., Bar-Haim E., Halperin G., Flashner Y., Cohen S., Shafferman A., Mamroud E. Yersinia pestis Endowed with increased cytotoxicity is avirulent in a bubonic plague model and induces rapid protection against pneumonic plague. PLoS ONE. 2009; 4(6):e5938.

51. Zhou D., Han Y., Yang R. Molecular and physiological insights into plague transmission, virulence and etiology. Microbes Infect. 2006; 8:273–84.

52. Yersin A. La peste bubonigue a Hong Kong. Ann. Inst. Pasteur (Paris). 1894; 8:662–7.


Review

For citations:


Bugorkova S.A., Devdariani Z.L., Shchukovskaya T.N., Kutyrev V.V. Historical and Modern Views on the Problem of Specific Plague Prophylaxis. Problems of Particularly Dangerous Infections. 2013;(3):63-69. (In Russ.) https://doi.org/10.21055/0370-1069-2013-3-63-69

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