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EVALUATION OF HUMORAL AND CELLULAR IMMUNITY LEVEL AMONG PERSONS LIVING IN THE CASPIAN NATURAL SANDY FOCUS TERRITORY AFTER ANTI-PLAGUE REVACCINATION

https://doi.org/10.15789/1563-0625-2018-2-241-250

Abstract

In view of increasing epidemic danger potential of some natural plague foci and performing measures to provide specific prevention of this infection, it becomes necessary to carefully monitor the state of immunity in vaccinated (revaccinated) individuals. The aim of the study was to assess humoral and cellular immunity levels in the persons after repeated anti-plague revaccination performed for appropriate epidemiological indications. Evaluation of immune responses to anti-plague revaccination was carried out according to studies of blood samples from 20 people aged 24 to 53 years living in the Caspian sandy natural plague focus located at the territory in Kalmykia Republic. Specific antibody titers to the F1 antigen of plague microbe were assessed in blood serum by immunoassay testing using an “ELISA-AT-F1 YERSINIA PESTIS” test system (Russian Research Anti-Plague Institute “Microbe”, Russia), along with spontaneous and concanavalin A-induced production of different cytokines, i.e., IFNγ, TNFα, IL-4, IL-10 (Vector-Best, Russia), IL-17A (Bender Medsystems, Austria). The studies were performed before vaccination, and 1, 6, 12 month after the booster vaccination.

The results of the study indicate that immunological reconstitution after revaccination with live plague vaccine occurs occurred mostly according to mixed Th1/Th2 type. Detection of antibodies to the F1 specific plague microbe antigen before and 1 month after revaccination (65 and 85%, respectively) was indicative of development of humoral response. The most informative cytokine markers (IFNγ and TNFα) for evaluation of an anti-plague cellular immune response have been identified. The threefold increase in IFNγ induced production before revaccination indicates to initial immunological competence of all the examined individuals. A high correlation between TNFα and other cytokine levels was determined. The fact of high correlation for the studied cytokines (TNFα, IFNγ, IL-10) indicated to a synchronism in the immunocompetent T helper cell reaction. By measuring the levels of spontaneous and induced cytokine production levels, one may indirectly judge on degree of anti-plague cell immunity in humans.

About the Authors

S. N. Klyueva
Russian Research Anti-Plague Institute “Microbe”
Russian Federation

PhD (Biology), Research Associate, Department of Immunology

410005, Russian Federation, Saratov, Universitetskaya str., 46. Phone: 7 (452) 26-21-31. Fax: 7 (452) 51-52-12



S. A. Bugorkova
Russian Research Anti-Plague Institute “Microbe”
Russian Federation
PhD, MD (Medicine), Head, Department of Immunology


T. N. Shchukovskaya
Russian Research Anti-Plague Institute “Microbe”
Russian Federation
PhD, MD (Medicine), Professor, Main Research Associate, Department of Immunology


D. N. Sandzhiev
Rospotrebnadzor Administration for the Republic of Kalmykia
Russian Federation

Head

Main State Sanitary Doctor of the Republic of Kalmykia



S. V. Konusheva
Rospotrebnadzor Administration for the Republic of Kalmykia
Russian Federation

Deputy Head

Deputy Main State Sanitary Doctor of the Republic of Kalmykia



S. P. Savchenko
Rospotrebnadzor Administration for the Republic of Kalmykia
Russian Federation
Head, Epidemiology Surveillance Department


B. A. Khasykova
Rospotrebnadzor Administration for the Republic of Kalmykia
Russian Federation
Deputy Head, Territorial Department “North-East”


S. A. Shcherbakova
Russian Research Anti-Plague Institute “Microbe”
Russian Federation
PhD, MD (Biology), Deputy Director


References

1. Балахонов С.В., Попова А.Ю., Мищенко А.И., Михайлов Е.П., Ежлова Е.Б., Демина Ю.В., Дени- сов А.В., Рождественский Е.Н., Базарова Г.Х., Щучинов Л.В., Зарубин И.В., Семенова Ж.Е., Маденова Н.М., Дюсенбаев Д.К., Ярыгина М.Б., Чипанин Е.В., Косилко С.А., Носков А.К., Корзун В.М. Случай заболевания человека чумой в Кош-Агачском районе республики Алтай в 2015 г. Сообщение 1. Клинико-эпидемиологические и эпизоотологические аспекты // Проблемы особо опасных инфекций, 2016. № 1. С. 55-60. [Balakhonov S.V., Popova A.Yu., Mishchenko A.I., Mikhaylov E.P., Ezhlova E.B., Demina Yu.V., Denisov A.V., Rozhdestvenskiy E.N., Bazarova G.Kh., Shchuchinov L.V., Zarubin I.V., Semenova Zh.E., Madenova N.M., Dyusenbaev D.K., Yarygina M.B., Chipanin E.V., Kosilko S.A., Noskov A.K., Korzun V.M. A Case of human infection with plague in the Kosh-Agach region of the republic of Altai in 2015. Communication 1. ClinicalEpidemiological and Epizootiological Aspects. Problemy osobo opasnykh infektsiy = Problems of Particularly Dangerous Infections, 2016, no. 1, pp. 55-60. (In Russ.)]

2. Фирстова В.В., Калмантаева О.В., Горбатов А.А., Кравченко Т.Б., Тюрин Е.А., Бондаренко Н.Л., Дятлов И.А., Караулов А.В. Оценка специфического гуморального и клеточного иммунитета у людей, периодически вакцинирующихся против чумы // Иммунопатология, аллергология, инфектология, 2015. №3. С. 62-68. [Firstova V.V., Kalmantaeva O.V., Gorbatov A.A., Kravchenko T.B., Tyurin E.A., Bondarenko N.L., Dyatlov I.A., Karaulov A.V. Specific humoral and cellular immunity in humans periodically vaccinated against plague. Immunopatologiya, allergologiya, infektologiya = International Journal of Immunopathology, Allergology, Infectology, 2015, no. 3, pp. 62-68. (In Russ.)]

3. Bi Y., Zhou J., Yang H., Wang X., Zhang X., Wang Q., Wu X., Han Y., Song Y., Tan Y., Du Z., Yang H., Zhou D., Cui Y., Zhou L., Yan Y., Zhang P., Guo Z., Wang X., Liu G., Yang R. IL-17A produced by neutrophils protects against pneumonic plague through orchestrating IFNg-activated macrophage programming. J. Immunol., 2014, Vol. 192, pp. 704-713.

4. Eriksson M., Sartono E., Martins C.L., Balé C., Garly M.L., Whittle H., Aaby P., Pedersen B.K., Yazdanbakhsh M., Erikstrup C., Benn C.S. A comparison of ex vivo cytokine production in venous and capillary blood. Clin. Exp. Immunol., 2007, Vol. 150, no. 3, pp. 469-476.

5. Levy Y., Flashner Y., Tidhar A., Zauberman A., Aftalion M., Lazar S., Gur D., Shafferman A., Mamroud E. T cells play an essential role in anti-F1 mediated rapid protection against bubonic plague. Vaccine, 2011, Vol. 29, no. 40, pp. 6866-6873.

6. Li B., Yang R. Interaction between Yersinia pestis and the host immune system. Infect. Immun., 2008, Vol. 76, no. 5, pp. 1804-1811.

7. Li B., Zhou L., Guo J., Wang X., Ni B., Ke Y., Zhu Z, Guo Z, Yang R. High-throughput identification of new protective antigens from a Yersinia pestis live vaccine by enzyme-linked immunospot assay. Infect. Immun., 2009, Vol. 77, no. 10, pp. 4356-4361.

8. Li B., Du C., Zhou Lei, Bi Y., Wang X., Wen L., Guo Z., Song Z., Yang R. Humoral and cellular immune responses to Yersinia pestis infection in long-term recovered plague patients. Clin. Vaccine Immunol., 2012, Vol. 19, no. 2, pp. 228-234.

9. Philipovskiy A.V., Smiley S.T. Vaccination with live Yersinia pestis primes CD4 and CD8 T Cells that synergistically protect against lethal pulmonary Y. pestis infection. Infection and Immunity, 2007, Vol. 75, no. 2, pp. 878-885.

10. Plotkin S.A. Correlates of Protection Induced by Vaccination. Clin. Vaccine Immunol., 2010, Vol. 17, no. 7, pp. 1055-1065.

11. Rajerison M., Dartevelle S., Ralafiarisoa L.A., Bitam I., Tuyet Dinh Thi Ngoc, Andrianaivoarimanana V., Nato F., Rahalison L. Development and evaluation of two simple, rapid immunochromatographic tests for the detection of Yersinia pestis antibodies in humans and reservoirs. PLoS Negl. Trop. Dis., 2009, Vol. 3, no. 4, e421. doi: 10.1371/journal.pntd.0000421.

12. Szaba F.M., Kummer L.W., Duso D.K., Koroleva E.P., Tumanov A.V., Cooper A.M., Bliska J.B., Smiley S.T., Lin J.S. TNFα and IFNγ but Not Perforin Are Critical for CD8 T Cell-Mediated Protection against Pulmonary Yersinia pestis Infection. PLoS Pathog., 2014. Vol. 10, no. 5, e1004142. doi:10.1371/journal.ppat.1004142.

13. Wang X., Wang Z., Guo Z., Wei B., Tian F., Yu S., Wang H., Wang H., Yang R. Serum cytokine responses in primary pneumonic plague patients. Clin. Vaccine Immunol., 2011, Vol. 18, no. 1, pp.184-186.

14. Williamson E.D., Flick-Smith H.C., LeButt C., Rowland C.A., Jones S.M., Waters E.L., Gwyther R.J., Miller J., Packer P.J., Irving M. Human immune response to a plague vaccine comprising recombinant F1 and V antigens. Infection and Immunity, 2005, Vol. 73, no. 6, pp. 3598-3608.

15. Williamson E.D. The role of immune correlates and surrogate markers in the development of vaccines and immunotherapies for plague. Advances in Preventive Medicine, 2012. Article ID 365980, 7 p. doi: 10.1155/2012/365980.


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For citations:


Klyueva S.N., Bugorkova S.A., Shchukovskaya T.N., Sandzhiev D.N., Konusheva S.V., Savchenko S.P., Khasykova B.A., Shcherbakova S.A. EVALUATION OF HUMORAL AND CELLULAR IMMUNITY LEVEL AMONG PERSONS LIVING IN THE CASPIAN NATURAL SANDY FOCUS TERRITORY AFTER ANTI-PLAGUE REVACCINATION. Medical Immunology (Russia). 2018;20(2):241-250. (In Russ.) https://doi.org/10.15789/1563-0625-2018-2-241-250

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