Preview

Humans and their health

Advanced search

The relationship of alveolar-bronchiolar disorders with the level of interleukin-20 in patients with community-acquired pneumonia

https://doi.org/10.21626/vestnik/2022-2/04

Abstract

Objective is to study the relationship between clinical, laboratory and radiological manifestations of alveolar-bronchiolar dysfunction with the production of interleukin-20 in patients with community-acquired pneumonia. Materials and methods. We examined 60 patients of both sexes aged 18 to 45 years with bacterial community-acquired pneumonia in the first 3 days of the disease, as well as 15 practically healthy individuals. The material of the study was venous blood, in the serum of which the concentration of interleukins (IL) was determined: IL-1β, -2, -4, -8, -10, -17A, -20, -28A, -33, tumor necrosis factor-alpha (TNFα), interferon-gamma (IFNγ), Clara cell protein (CCP), surfactant protein D (SP-D), prostacyclin (PgI2), soluble form of the Fas-receptor (sFas), and its ligand (sFasL), leukotriene D4 (LTD4), thromboxane A2 (TA2). Results. The development of pneumonia is accompanied by an increase in the production of the studied mediators, which is more pronounced in patients with a severe course of the disease. An increase in the concentration of IL-20 from the minimum to the maximum level is accompanied by a significant proportional decrease in the concentration of IL-1β, TNFα, IL-33, TA2, LTD4, Fas, FasL. A high level of IL-20 was associated with a decrease in the concentration of CCP, indicating a weakening of the alveolar-bronchiolar dysfunction and a decrease in the intensity of the inflammatory reaction in the lung tissue. It was also found that a high level of IL-20 was associated with increased production of PgI2, IFNγ, IL-1RA, IL-17A, IL-8, IL-4, IL-28A, IL-10, SLPI. Conclusion. The results of the study indicate the important role of IL-20 in the development of inflammation of the lower respiratory tract, which consists in regulating the activity of the acute phase response, modulating the production of prostacyclin and leukotrienes, determining the limitation of alveolar-bronchiolar dysfunction in patients with pneumonia, as well as the restriction of proapoptogenic influences that determine the decrease in volumes. tissue and cellular damage in such patients.

About the Authors

Stanislav S. Bondar
Kaluga Regional Clinical Hospital (KRCH)
Russian Federation

therapist; KRCH, Kaluga, Russian Federation



Igor V. Terekhov
K.E. Tsiolkovsky Kaluga State University nam (K.E. Tsiolkovsky KSU)
Russian Federation

Cand. Med. (Sci.), Associate Professor of the Department of Internal Diseases, K.E. Tsiolkovsky KSU, Kaluga, Russian Federation



Vladimir K. Parfenyuk
V.I. Razumovsky Saratov State Medical University (V.I. Razumovsky SSMU)
Russian Federation

Dr. Sci. (Med.), Full Professor, Professor of the Department of Faculty Therapy, V.I. Razumovsky SSMU, Saratov, Russian Federation



Nelli V. Bondar


References

1. Ketlinskiy S.A., Simbirtsev A.S. Cytokines. Saint-Peterburg: LLO “Foliant”, 2008. 552 p. (in Russ.)

2. Zhang J., Tecson K.M., McCullough P.A. Endothelial dysfunction contributes to COVID-19-associated vascular inflammation and coagulopathy. Rev Cardiovasc Med. 2020;21(3):315-319. DOI: 10.31083/j.rcm.2020.03.126

3. Flori H., Sapru A., Quasney M.W., Gildengorin G., Curley M.A.Q., Matthay M.A., Dahmer M.K.; BALI and RESTORE Study Investigators et al. A prospective investigation of interleukin-8 levels in pediatric acute respiratory failure and acute respiratory distress syndrome. Crit Care. 2019;23(1):128. DOI: 10.1186/s13054-019-2342-8

4. Jerkic M., Masterson C., Ormesher L., Gagnon S., Goyal S., Rabani R., Otulakowski G. et al. Overexpression of IL-10 Enhances the Efficacy of Human Umbilical-Cord-Derived Mesenchymal Stromal Cells in E. coli Pneumosepsis. J Clin Med. 2019;8(6):847. DOI: 10.3390/jcm8060847

5. Kharlamova O.S., Nikolaev K.Yu., Ragino Yu.I., Voevoda M.I. Surfactant proteins A and D: role in the pathogenesis of community-acquired pneumonia and possible predictive perspectives. Terapevticheskii arkhiv. 2020;92(3):109-115 (in Russ.). DOI: 10.26442/00403660.2020.03.000275. EDN: INIXUH

6. Pugach V.A., Tyunin M.A., Vlasov T.D., Il’inskiy N.S., Gogolevskiy A.S., Chepur S.V. Biomarkers of acute respiratory distress syndrome: problems and prospects of their application. Messenger of Anesthesiology and Resuscitation. 2019;16(4):38-46 (in Russ.). DOI: 10.21292/2078-5658-2019-16-4-38-46. EDN: TLIFEB

7. Wegenka U.M. IL-20: biological functions mediated through two types of receptor complexes. Cytokine Growth Factor Rev. 2010;21(5):353-363. DOI: 10.1016/j.cytogfr.2010.08.001

8. Gough P., Ganesan S., Datta S.K. IL-20 Signaling in Activated Human Neutrophils Inhibits Neutrophil Migration and Function. J Immunol. 2017;198(11): 4373-4382. DOI: 10.4049/jimmunol.1700253

9. Hsu Y.H., Li H.H., Hsieh M.Y., Liu M.F., Huang K.Y., Chin L.S., Chen P.C., Cheng H.H. et al. Function of interleukin-20 as a proinflammatory molecule in rheumatoid and experimental arthritis. Arthritis Rheum. 2006;54(9):2722-2733. DOI: 10.1002/art.22039

10. Burgoyne R.A., Fisher A.J., Borthwick L.A. The Role of Epithelial Damage in the Pulmonary Immune Response. Cells. 2021;10(10):2763. DOI: 10.3390/cells10102763

11. Moroz V.V., Golubev A.M., Kuzovlev A.N., Shabanov A.K., Pisarev V.M. Clara cell protein (club cell protein) is a new diagnostic molecular candidate biomarker in nosocomial pneumonia. General Reanimatology. 2014;10(6):6-14 (in Russ.). DOI: 10.15360/1813-9779-2014-6-6-14. EDN: TEGAOV

12. Gough P., Ganesan S., Datta S.K. IL-20 Signaling in Activated Human Neutrophils Inhibits Neutrophil Migration and Function. J Immunol. 2017;198(11):4373-4382. DOI: 10.4049/jimmunol.1700253

13. Ha H.L., Wang H., Claudio E., Tang W., Siebenlist U. IL-20-Receptor Signaling Delimits IL-17 Production in Psoriatic Inflammation. J Invest Dermatol. 2020;140(1):143-151.e3. DOI: 10.1016/j.jid.2019.06.127

14. Lv R., Zhao J., Lei M., Xiao D., Yu Y., Xie J. IL-33 Attenuates Sepsis by Inhibiting IL-17 Receptor Signaling through Upregulation of SOCS3. Cell Physiol Biochem. 2017;42(5):1961-1972. DOI: 10.1159/000479836

15. Burmeister A.R., Johnson M.B., Marriott I. Murine astrocytes are responsive to the pro-inflammatory effects of IL-20. Neurosci Lett. 2019;708:134334. DOI: 10.1016/j.neulet.2019.134334

16. Uto-Konomi A., Miyauchi K., Ozaki N., Motomura Y., Suzuki Y., Yoshimura A., Suzuki S., Cua D. et al. Dysregulation of suppressor of cytokine signaling 3 in keratinocytes causes skin inflammation mediated by interleukin-20 receptor-related cytokines. PLoS One. 2012;7(7):e40343. DOI: 10.1371/journal.pone.0040343

17. Kolumam G., Wu X., Lee W.P., Hackney J.A., Zavala-Solorio J., Gandham V., Danilenko D.M., Arora P. et al. IL-22R Ligands IL-20, IL-22, and IL-24 Promote Wound Healing in Diabetic db/db Mice. PLoS One. 2017;12(1):e0170639. DOI: 10.1371/journal.pone.0170639

18. Chen J., Caspi R.R., Chong W.P. IL-20 receptor cytokines in autoimmune diseases. J Leukoc Biol. 2018;104(5):953-959. DOI: 10.1002/JLB.MR1117-471R

19. Aarts J., Roeleveld D.M., Helsen M.M., Walgreen B., Vitters E.L., Kolls J., van de Loo F.A., van Lent P.L. et al. Systemic overexpression of interleukin-22 induces the negative immune-regulator SOCS3 and potently reduces experimental arthritis in mice. Rheumatology (Oxford). 2021;60(4):1974-1983. DOI: 10.1093/rheumatology/keaa589

20. Gao Y., Zhao H., Wang P., Wang J., Zou L. The roles of SOCS3 and STAT3 in bacterial infection and inflammatory diseases. Scand J Immunol. 2018;88(6):e12727. DOI: 10.1111/sji.12727

21. Tsukada J., Yoshida Y., Kominato Y., Auron P.E. The CCAAT/enhancer (C/EBP) family of basic-leucine zipper (bZIP) transcription factors is a multifaceted highly-regulated system for gene regulation. Cytokine. 2011;54(1):6-19. DOI: 10.1016/j.cyto.2010.12.019

22. Khaitov R.M., Pinegin B.V., Pashenkov M.V. Epithelial cells of the respiratory tract as equal participants of innate immunity and potential targets for immunotropic drugs. Immunologiya. 2020;41(2):107-113 (in Russ.). DOI: 10.33029/0206-4952-2020-41-2-107-113. EDN: YQOZRL

23. Dong C. Cytokine Regulation and Function in T Cells. Annu Rev Immunol. 2021;39:51-76. DOI: 10.1146/annurev-immunol-061020-053702

24. Bondar S.S., Terekhov I.V., Nikiforov V.S. The relationship of JAK/STAT and MAPK/SAPK signaling pathways, NF-kB and content in the mononuclear cells of whole blood thioredoxins in the post-clinical stage of community-acquired pneumonia. Consilium Medicum. 2018;20(11):61-65. (in Russ.). DOI: 10.26442/20751753.2018.11.180091. EDN: YTBUQP

25. Terekhov I.V., Nikiforov V.S., Bondar' S.S. Condition of RIG-I and NF-KB-signal pathways in mononuclear cells of whole blood of practically healthy people and reconvalescents of pneumonia affected by mitogenic stimulation. Genes & cells. 2019;14(3):131-136 (in Russ.). DOI: 10.23868/201906023. EDN: AOWMIK

26. Titova O.N., Kuzubova N.A., Lebedeva E.S., Volchkova E.V. Regeneration potential activation of lung tissue in severe community-acquired pneumonia. RMJ. 2020;28(4):24-28 (in Russ.). EDN: MTXIZA

27. Terekhov I.V. Solodukhin K.A., Nikiforov V.S. Features of the biological effect of low-intensity microwave irradiation in conditions of antigenic stimulation of mononuclear cells of whole blood. Fizioterapevt. 2013;(1):26-32 (in Russ.)


Review

For citations:


Bondar S.S., Terekhov I.V., Parfenyuk V.K., Bondar N.V. The relationship of alveolar-bronchiolar disorders with the level of interleukin-20 in patients with community-acquired pneumonia. Humans and their health. 2022;25(2):31-42. (In Russ.) https://doi.org/10.21626/vestnik/2022-2/04

Views: 278


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 1998-5746 (Print)
ISSN 1998-5754 (Online)