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Immunoadjuvant activity of marine bacteria exopolysaccharides in normal and immunosuppressive conditions

https://doi.org/10.37489/0235-2990-2021-66-5-6-17-22

Abstract

Aim. To assess the mechanisms of immunoadjuvant activity of marine bacteria exopolysaccharides (PS) in normal and immunosuppressive conditions in vivo. Material and methods. Experimental studies were carried out on male ВALB/c mice, immunized with compositions of PS or aluminum hydroxide and ovalbumin (OVA). Immunosuppression was induced by triple intraperitoneal administration of dexamethasone (2 mg/kg). Serum levels of specific antibodies (IgG, IgG1, and IgG2a) and cytokines (IFN-γ, IL-2, IL-10) were determined. Results. The inclusion of PS to the immune compositions led to the formation of an enhanced specific IgG, IgG1, and IgG2a to OVA, comparable to the effect of aluminum hydroxide. The studied PS also contributed to an increase in the level of both pro- and anti-inflammatory cytokines. Conclusion. PS from marine bacteria act as adjuvants in normal and immunosuppressive conditions, stimulating a mixed Th1 (IgG2a, INF-γ) and Th2 (IgG1, IL-10) immune response to OVA.

About the Authors

T. A. Kuznetsova
G. P. Somov Research Institute of Epidemiology and Microbiology
Russian Federation

Tatyana A. Kuznetsova — D. Sc. in medicine

ResearcherID: I-8399-2018; eLIBRARY SPIN code: 2359-1132; Scopus Author ID: 7202571979

1 Selskaya, G. P. Somov Research Institute of Epidemiology and Microbiology, Vladivostok



E. V. Persiyanova
G. P. Somov Research Institute of Epidemiology and Microbiology
Russian Federation

Elena V. Persiyanova — Ph. D. in biology

ResearcherID: I-3513-2018; eLIBRARY SPIN: 8385-7621; Scopus Author ID: 56311963200

Vladivostok



L. A. Ivanushko
G. P. Somov Research Institute of Epidemiology and Microbiology
Russian Federation

Lyudmila A. Ivanushko — Ph. D. in medicine

ResearcherID: K-2879-2018; eLIBRARY SPIN: 1535-7665; Scopus Author ID: 6507058048

Vladivostok



T. P. Smolina
G. P. Somov Research Institute of Epidemiology and Microbiology
Russian Federation

Tatyana P. Smolina — Ph. D. in biology

ResearcherID: J-4344-2018; eLIBRARY SPIN code: 3503-8898; Scopus Author ID: 6603763859

Vladivostok



A. K. Gazha
G. P. Somov Research Institute of Epidemiology and Microbiology
Russian Federation

Anna K. Gazha — Ph. D. in medicine

ResearcherID: J-4350-2018; eLIBRARY SPIN code: 1960-4471; Scopus Author ID: 6508049418

Vladivostok



M. S. Kokulin
G. B. Elyakov Pacific Institute of Bioorganic Chemistry
Russian Federation

Maksim S. Kokulin — Ph. D. in chemistry

ResearcherID: N-8353-2013; eLIBRARY SPIN: 9170-5830; Scopus Author ID: 54410589100

Vladivostok



N. N. Besednova
G. P. Somov Research Institute of Epidemiology and Microbiology
Russian Federation

Natalia N. Besednova — D.Sc. in medicine, Professor, Academician of the Russian Academy of Sciences, G. P. Somov Research Institute of Epidemiology and Microbiology

eLIBRARY SPIN: 8931-9002; Scopus Author ID: 7006805123

Vladivostok



References

1. Persing D.H., Coler R.N., Lacy M.J., Johnson D.A., Baldridge J.R., Hershberg R.M., Reed S.G. Taking toll: Lipid A mimetics as adjuvants and immunomodulators. Trends Microbiol. 2002; 10: s32–s37. doi: 10.1016/s0966-842x(02)02426-5.

2. Casella C.R., Mitchell T.C. Putting endotoxin to work for us: Monophosphoryl lipid A as a safe and effective vaccine adjuvant. Cell Mol Life Sci. 2008; 65: 3231. doi: 10.1007/s00018-008-8228-6.

3. Kamphuis T., Meijerhof T., Stegmann T., Lederhofer J., Wilschut J., de Haan A. Immunogenicity and protective capacity of a virosomal respiratory syncytial virus vaccine adjuvanted with monophosphoryl lipid A in mice. PLoS ONE. 2012; 7: e36812. doi: 10.1371/journal.pone.0036812.

4. Tota J.E., Struyf F., Sampson J.N., Gonzalez P., Ryser M., Herrero R. et al. Efficacy of the AS04-adjuvanted HPV-16/18 vaccine: pooled analysis of the Costa Rica Vaccine and PATRICIA randomized controlled trials. J Natl Cancer Inst. 2020; 112: 818–828. doi: 10.1093/jnci/djz222.

5. Moscovici M. Present and future medical applications of microbial exopolysaccharides. Front Microbiol 2015; 6: 1012–1022. doi: 10.3389/fmicb.2015.01012.

6. Lin M.H., Yang Y.L., Chen Y.P., Hua K.-F., Lu C.-P., Sheu F. et al. A novel exopolysaccharide from the biofilm of Thermusaquaticus YT-1 induces the immune response through Toll-like receptor 2. J Biol Chem. 2011; 286 (20): 17736–45. doi: 10.1074/jbc.M110.200113.

7. Yu L., Sun G., Wei J., Wang Y., Du C., Li J. Activation of macrophages by an exopolysaccharide isolated from Antarctic Psychrobacter sp. B-3. Chinese J. of Oceanology and Limnology 2016; 34 (5): 1064–71. doi:10.1007/s00343-016-4393-x.

8. Bai Y., Zhang P., Chen G., Cao J., Huang T., Chen K. Macrophage immunomodulatory activity of extracellular polysaccharide (PEP) of Antarctic bacterium Pseudoaltermonas sp. S-5. Int Immunopharmacol. 2012; 12 (4): 611–617. doi: 10.1016/j.intimp.2012.02.009.

9. Kokoulin M.S., Kuzmich A.S., Kalinovsky A.I., Tomshich S.V., Romanenko L.A., Mikhailov V.V., Komandrova N.A. Structure and anticancer activity of sulfated O-polysaccharide from marine bacterium Cobetia litoralis KMM 3880T. Carbohydr Polym. 2016; 154: 55–61. doi: 10.1016/j.carbpol.2016.08.036.

10. Kokoulin M.S., Komandrova N.A., Kalinovsky A.I., Tomshich S.V., Romanenko L.A., Vaskovsky V.V. Idiomarina abyssalis КММ 227T containing a 2-O-sulfate-3-N-(4-hydroxybutanoyl)-3,6-dideoxy-d-glucose. Carbohydr Res. 2015; 41: 100-6. doi: 10.1016/j.carres.2015.05.012.

11. Bogacheva N.V., Tuneva N.A., Smirnov A.A., Galyamova D.A., Popesku L.I. Razrabotka biologicheskoi modeli immunosupressii pri pomoschi deksametazona. Vyatskii Medicinskii Vestnik 2018; 4 (60): 39–43. (in Russian)

12. Seder R.A., Hill A.V. Vaccines against intracellular infections requiring cellular immunity. Nature 2000; 406: 793–798. doi: 10.1038/35021239.

13. McKee A.S., Munks M.W., Marrack P. How do adjuvants work? Important considerations for new generation adjuvants. Immunity. 2007; 27: 687–690. doi: 10.1016/j.immuni.2007.11.003.

14. Coffman R.L., Sher A., Seder R.A. Vaccine Adjuvants: Putting Innate Immunity to Work. Immunity 2010; 33 (4): 492–503. doi: 10.1016/j.immuni.2010.10.002.

15. Xie Y., Tolmeijer S., Oskam J.M., Tonkens T., Meijer A.H., Schaaf M.J.M. Glucocorticoids inhibit macrophage differentiation towards a pro-inflammatory phenotype upon wounding without affecting their migration. Disease Models & Mechanisms. 2019; 12: dmm037887. doi: 10.1242/dmm.037887.

16. Cain D.W., Cidlowski J.A. Immune regulation by glucocorticoids. Nat Rev Immunol 2017: 17: 233–247. doi: 10.1038/nri.2017.1.

17. Ma W., Gee K., Lim W., Chambers K., Angel J.B., Kozlowski M., Kumar A. Dexamethasone inhibits IL-12p40 production in lipopolysaccharide-stimulated human monocytic cells by down-regulating the activity of c-Jun N-terminal kinase, the activation protein-1, and NF-kappa B transcription factors. J Immunol. 2004; 172: 318–30. doi: 10.4049/jimmunol.172.1.318.

18. Vormehr M., Lehar S., Kranz L.M., Tahtinen S., Oei Y., Javinal V. et al. Dexamethasone premedication suppresses vaccine-induced immune responses against cancer. OncoImmunology. 2020; 9 (1): е1758004. DOI: 10.1080/2162402X.2020.1758004.


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For citations:


Kuznetsova T.A., Persiyanova E.V., Ivanushko L.A., Smolina T.P., Gazha A.K., Kokulin M.S., Besednova N.N. Immunoadjuvant activity of marine bacteria exopolysaccharides in normal and immunosuppressive conditions. Antibiot Khimioter = Antibiotics and Chemotherapy. 2021;66(5-6):17-22. (In Russ.) https://doi.org/10.37489/0235-2990-2021-66-5-6-17-22

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