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Levels of proinflammatory cytokines IL-1β, IL-6, TNF, INF-γ in children with different clinical forms of rotavirus infection

https://doi.org/10.52485/19986173_2023_1_1

Abstract

   Aim. To investigate the concentration of cytokines IL- 1β, IL-6, TNF- α, INF- γ in the peripheral blood of children with different clinical forms of rotavirus infection using flow cytofluorimetry.

   Materials and methods. 32 patients with moderate rotavirus infection aged 15 to 36 months were examined, 18 of them without inflammation of the upper respiratory tract (1st group, mean age 27 [22; 33] months) and 14 children with symptoms of upper respiratory tract inflammation (group 2, mean age 30 [27; 31] months). Control group - 19 children of the same age - 23 [20; 31] months. In serum of all children were determined: IL-1β, IL-6, TNF-α, INF-γ. Cytokine concentrations were evaluated by flow fluorimetry. The obtained data were processed using the «STATISTICA-10» software package, Microsoft Excel 2010.

   Results. Serum concentrations of IL-1β, TNF-α, INF-γ cytokines were found to be increased in children regardless of the presence or absence of respiratory catarrhal syndrome in rotavirus infection compared to controls. The higher levels of IL-6, INF-γ were reported in serum, which were positively correlated with a clinic of rotavirus infection accompanied by symptoms of upper respiratory tract inflammation.

   Conclusions. The IL-6, serum INF-γ study may serve as an additional diagnostic criterion for extra-intestinal lesion in children with rotavirus infection.

About the Authors

E. V. Andreeva
Chita State Medical Academy
Russian Federation

672000; 39a Gorky Street; Chita



N. A. Miromanova
Chita State Medical Academy
Russian Federation

672000; 39a Gorky Street; Chita



P. P. Tereshkov
Chita State Medical Academy
Russian Federation

672000; 39a Gorky Street; Chita



References

1. World Health Organization (WHO). Levels and Trends in Child Mortality Report 2019. [Electronic resource]. Access mode: https://documents1.worldbank.org/curated/en/105841568905930695/pdf/Levels-and-Trends-in-Child-Mortality-Report-2019.pdf (7 Feb 2023).

2. Norboev I.M. On the role of rotaviruses in the occurrence of acute diarrheal diseases in children in Uzbekistan. Epidemiologiya i infekcionnye bolezni. 2018. 23(5). С. 239-241. DOI: 10.18821/1560-9529-2018-23-5-239-241. in Russian.

3. Hartman S., Brown E., Loomis E., Russell H.A. Gastroenteritis in children. AmFamPhysician. 2019. 99. 159-165.

4. Bedelbaev M.K., Dzholbunova Z.K., Halupko E.A. Comparative clinical and epidemiological characteristics of rotavirus infection in young children. Bulletin of science and practice. 2020. 6(4). 135-146. DOI: 10.33619/2414-2948/53/17. in Russian.

5. Pron'ko N.V. Modern aspects of acute intestinal infections of viral etiology in children. Aktual'naya infektologiya. 2018. 6(2). 93-97. DOI: 10.22141/2312-413x.6.2.2018.131096. in Russian.

6. Andreeva E.V., Miromanova N.A., Nikiforova T.F. The place of rotavirus infection in the structure of acute intestinal infections in hospitalized children of the first year of life in Chita. Zabajkal'skij medicinskij vestnik. 2022. 2. 8-15. DOI: 10.52485/19986173_2022_2_8. in Russian.

7. Chiappini E., Azzari C., Moriondo M., Galli L., deMartino M. Viraemia is a common finding in immunocompetent children with rotavirus infection. J. Med. Virol. 2005. 76. 265-267. DOI: 10.1002/jmv.20351.

8. Azevedo M.S., Yuan L., Jeong K.I., et al. Viremia and nasal and rectal shedding of rotavirus in gnotobiotic pigs inoculated with human rotavirus. J. Virol. 2005. 79. 5428-5436. DOI: 10.1128/JVI.79.9.5428-5436.2005.

9. McCormack J.G. Clinical features of rotavirus gastroenteritis. J Infect. 1982 Mar. 4(2). 167-74. DOI: 10.1016/s0163-4453(82)93777-x.

10. Muhina A.A., SHipulin G.A., Bokovoj A.G. i dr. Epidemiologiya i infekcionnye bolezni. 2002. 2. 43-47. in Russian.

11. Gómez-Rial J., Curras-Tuala M.J., Rivero-Calle I., Rodríguez-Tenreiro C., Redondo-Collazo L., Gómez-Carballa A., Pardo-Seco J., Salas A., Martinón-Torres F. Rotavirus intestinal infection induces an oral mucosa cytokine response. PLoS One. 2018. 13(4). 0195314. DOI: 10.1371/journal.pone.0195314.

12. Carlson J.A., Middleton P.J., Szymanski M.T., Huber J., Petric M. Fatal rotavirus gastroenteritis: an analysis of 21 cases. Am. J. Dis. Child. 1978. 132. 477-479. DOI: 10.1001/archpedi.1978.02120300037006.

13. Rollo E.E., Kumar K.P., Reich N.C., Cohen J., Angel J., Greenberg H. B., Sheth R., Anderson J., Oh B., Hempson S.J., Mackow E.R., Shaw R.D. The epithelial cell response to rotavirus infection. J. Immunol. 1999. 163. 4442-4452. PMID: 10510386.

14. Wang X., Yang Q., Zhou X., Chen T., Dou L., Wang F., Wang W. Shenling Baizhu Powder Inhibits RV-SA11-Induced Inflammation and Rotavirus Enteritis via TLR4/MyD88/NF-κB Signaling Pathway. Front Pharmacol. 2021. 12. 642-685. DOI: 10.3389/fphar.2021.642685.

15. Liu P., Zou R., Zhao J., Hao J., Zeng Y., Liu W., Tian J., Wang H. Changes in humoral immunity, myocardial damage, trace elements, and inflammatory factor levels in children with rotavirus enteritis. Am J Transl Res. 2022 Jan 15. 14(1). 452-459. PMID: 35173864; PMCID: PMC8829652.

16. Khalil R.G., Abdel-Moneim A., Arafa A.A., Allam G., El-Senousy W.M., Mabrouk D. Possible association of rotavirus IgG with cytokine expression levels and dyslipidemia in rotavirus-infected type 1 diabetic children. Mol Biol Rep. 2022. 49(8). 7587-7599. DOI: 10.1007/s11033-022-07573-0.

17. Malik J., Gupta S.K., Bhatnagar S., Bhan M.K., Ray P. Evaluation of IFN-gamma response to rotavirus and non-structural protein NSP4 of rotavirus in children following sev.8.06.014. Epub 2008 Aug 6. DOI: 10.1016/j.jcv.2008.06.014.

18. Turner M.D. Cytokines and chemokines: At the crossroads of cell signaling and inflammatory disease. Biochimica et BiophysicaActa. 2014. 1843. 2563-2582. DOI: 10.1016/j.bbamcr.2014.05.014.

19. Mormile R. Severe gastroenteritis and acute pancreatitis following rotavirus infection in children: the age-related failure of IFN-γ. ImmunolLett. 2016. 175. 58–59. DOI: 10.1016/j.imlet.2016.04.017.

20. FGBU NIIDI FMBA ROSSII, Public organization "Eurasian Society for Infectious Diseases," Public organization "Association of Infectious Disease Doctors of St. Petersburg and the Leningrad Region" (AVISPO). Clinical guidelines (treatment protocol) for the provision of medical care to children with rotavirus infection. 2015. [Electronic resource]. Access mode: http://niidi.ru/dotAsset/91e2802d-ed31-40a1-b32b-c888f12c196c.pdf. (7 Feb 2023). in Russian.

21. Hakim M.S., Ding S., Chen S., Yin Y., Su J., van der Woude C.J., Fuhler G.M., Peppelenbosch M.P., Pan Q., Wang W. TNF-α exerts potent anti-rotavirus effects via the activation of classical NF-κB pathway. Virus Res. 2018 Jul 15. 253. 28-37. DOI: 10.1016/j.virusres.2018.05.022.

22. Jiang B., Snipes-Magaldi L., Dennehy P., Keyserling H., Holman R.C., Bresee J. et al. Cytokines as mediators for or effectors against rotavirus disease in children. Clin Diagn Lab Immunol, 2003. 10(6). 995-1001. DOI: 10.1128/cdli.10.6.995-1001.2003.

23. Chen S.M., Lin C.P., Tsai J.D., Chao Y.H., Sheu J.N. The significance of serum and fecal levels of interleukin-6 and interleukin-8 in hospitalized children with acute rotavirus and norovirus gastroenteritis. PediatrNeonatol. 2014. 55(2). 120-126. DOI: 10.1016/j.pedneo.2013.05.008.


Review

For citations:


Andreeva E.V., Miromanova N.A., Tereshkov P.P. Levels of proinflammatory cytokines IL-1β, IL-6, TNF, INF-γ in children with different clinical forms of rotavirus infection. Transbaikalian Medical Bulletin. 2023;(1):1-9. (In Russ.) https://doi.org/10.52485/19986173_2023_1_1

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