Features of the cytokine profile repolarization in the patients with chronic rhinosinusitis and comorbid conditions
https://doi.org/10.15789/1563-0625-FOT-3259
Abstract
Rhinosinusitis is one of the most common diseases in otolaryngology which manifests itself as nasal congestion, headache, nasal discharge and other symptoms. Sometimes rhinosinusitis accompanies seasonal acute respiratory viral infections, being a manifestation of seasonal and year-round allergies, and develops with dysfunction of the immune response. Chronic rhinosinusitis (CRS) is diagnosed if the symptoms of rhinosinusitis last for >12 weeks. Comorbid conditions (curvature of the nasal septum, bronchial asthma, etc.) increase the manifestations of CRS. The purpose of our work was to study the features of cytokine regulation in CRS with comorbid diseases. 84 persons with rhinosinusitis and 100 healthy controls were involved. The study included patients with CRS (n = 29), CRS and deviated septum (n = 24), CRS with bronchial asthma (n = 31) and a control group (n = 100) consisting of practically healthy individuals. The case–control study was performed in Laboratory of Clinical Pathophysiology at the Research Institute of the Railway Ministry. The studied materials were venous blood and nasal discharge. The content of TNFα, IFNγ, IL-2, IL-6, IL-4, IL-10 was determined by ELISA technique using JSC "Vector-Best" reagents (Novosibirsk, Russia) and a Muitiskan FC spectrophotometer. Statistical processing was performed using the Statistica 10.0 program. To describe samples with a distribution different from normal, we used the median (Me) and interquartile range (IQR), defined as the difference between the 25th (Q0.25) and 75th (Q0.75) percentiles. This approach allows us to present the central tendency and measure of data dispersion, minimizing the impact of outliers (Wilcox, 2012). All patients with CRS and comorbid conditions systemically and locally show unidirectional changes manifesting as an increase in proand anti-inflammatory cytokines, thus suggesting the development of immune responses by Th1/Th2 mechanisms. The presence of comorbid conditions (curvature of the nasal septum, bronchial asthma) enhances the immune response. In comorbid conditions, the content of cytokines is statistically significantly increased relative to both control group and patients with CRS. Maximum concentrations of cytokines are detected when CRS was combined with bronchial asthma.
About the Authors
A. M. LazarevaRussian Federation
PhD (Medicine), Senior Researcher, Laboratory of Clinical Pathophysiology, Research Institute of Medical Problems of the North, Krasnoyarsk Research Center, Siberian Branch, RAS; Associate Professor, Department of Medical Biology, Institute of Fundamental Biology and Biotechnology, SFU.
Krasnoyarsk
Competing Interests:
none
O. V. Smirnova
Russian Federation
PhD, MD (Medicine), Professor, Head, Laboratory of Clinical Pathophysiology, Research Institute of Medical Problems of the North, Krasnoyarsk Research Center, Siberian Branch, RAS; Head, Department of Medical Biology, Institute of Fundamental Biology and Biotechnology, SFU.
Krasnoyarsk
Competing Interests:
none
References
1. Astafyeva N.G. Rhinitis: immune and non-immune bases of a heterogeneous syndrome. Vestnik terapevta = Therapist’s Bulletin, 2019, no. 2. [Electronic resource]. Available at: https://journal.therapy.school/statyi/rinity-immunnye-i-neimmunnyeosnovy-geterogennogo-sindroma/ (date of access: January 24, 2025) (In Russ.)
2. Isaev P.Yu., Климов V.V., Romanova M.I., Sviridova V.S., Naidina O.A., Pronina N.A. “Skin window” cytokines in bronchial asthma associated with food allergy. Rossiyskiy immunologicheskiy zhurnal = Russian Journal of Immunology, 2018, Vol. 12, no. 3, pp. 317-320. (In Russ.) doi: 10.31857/S102872210002402-7.
3. Trushina E.Y., Kostina E.M., Baranova N.I., Tipikin V.A. The cytokines role as inflammation molecular markers in non-allergic bronchial asthma. Sovremennye problemy nauki i obrazovaniya = Modern Problems of Science and Education, 2018, no. 4. [Electronic resource]. Available at: https://science-education.ru/ru/article/view?id=27799 (date of access: January 28, 2025) (In Russ.)
4. Boita M., Bucca C., Riva, G., Heffler E. Release of Type 2 Cytokines by Epithelial Cells of Nasal Polyps. J. Immunol. Res., 2016, Vol. 2016, 2643297. doi: 10.1155/2016/2643297.
5. Fokkens W.J., Lund V.J., Hopkins C., Hellings P.W., Kern R., Reitsma S., Toppila-Salmi S., BernalSprekelsen M., Mullol J., Alobid I., Anselmo-Lima W.T., Bachert C., Baroody F., von Buchwald C., Cervin A., Cohen N., Constantinidis J., De Gabory L., Desrosiers M., Diamant Z., Douglas R.G., Gevaert P.H., Hafner A., Harvey R.J., Joos G.F., Kalogjera L., Knill A., Kocks J.H., Landis B.N., Limpens J., Lebeer S., Lourenco O., Meco C., Matricardi P.M., O'Mahony L., Philpott C.M., Ryan D., Schlosser R., Senior B., Smith T.L., Teeling T., Tomazic P.V., Wang D.Y., Wang D., Zhang L., Agius A.M., Ahlstrom-Emanuelsson C., Alabri R., Albu S., Alhabash S., Aleksic A., Aloulah M., Al-Qudah M., Alsaleh S., Baban M.A., Baudoin T., Balvers T., Battaglia P., Bedoya J.D., Beule A., Bofares K.M., Braverman I., Brozek-Madry E., Richard B., Callejas C., Carrie S., Caulley L., Chussi D., de Corso E., Coste A., El Hadi U., Elfarouk A., Eloy P.H., Farrokhi S., Felisati G., Ferrari M.D., Fishchuk R., Grayson W., Goncalves P.M., Grdinic B., Grgic V., Hamizan A.W., Heinichen J.V., Husain S., Ping T.I., Ivaska J., Jakimovska F., Jovancevic L., Kakande E., Kamel R., Karpischenko S., Kariyawasam H.H., Kawauchi H., Kjeldsen A., Klimek L., Krzeski A., Kopacheva Barsova G., Kim S.W., Lal D., Letort J.J., Lopatin A., Mahdjoubi A., Mesbahi A., Netkovski J., Nyenbue Tshipukane D., Obando-Valverde A., Okano M., Onerci M., Ong Y.K., Orlandi R., Otori N., Ouennoughy K., Ozkan M., Peric A., Plzak J., Prokopakis E., Prepageran N., Psaltis A., Pugin B., Raftopulos M., Rombaux P., Riechelmann H., Sahtout S., Sarafoleanu C.-C., Searyoh K., Rhee C.-S., Shi J., Shkoukani M., Shukuryan A.K., Sicak M., Smyth D., Sindvongs K., Soklic Kosak T., Stjarne P., Sutikno B., Steinsvag S., Tantilipikorn P., Thanaviratananich S., Tran T., Urbancic J., Valiulius A., de Aparicio C.V., Vicheva D., Virkkula P.M., Vicente G., Voegels R., Wagenmann M.M., Wardani R.S., Welge-Lussen A., Witterick I., Wright E., Zabolotniy D., Zsolt B., Zwetsloot C.P. European Position Paper on Rhinosinusitis and Nasal Polyps 2020. Rhinology, 2020, Vol. 58, Suppl. S29, pp. 1-464.
6. Jiao J., Duan S., Meng N., Li Y., Fan E. Role of IFN-γ, IL-13, and IL-17 on mucociliary differentiation of nasal epithelial cells in chronic rhinosinusitis with nasal polyps. Clin. Exp. Allergy, 2016, Vol. 46, no. 3, pp. 449-460.
7. Klingler A.I., Stevens W.W., Tan B.K., Peters A.T., Poposki J.A., Grammer L.C., Welch K.C., Smith S.S., Conley D.B., Kern R.C., Schleimer R.P., Kato A. Mechanisms and biomarkers of inflammatory endotypes in chronic rhinosinusitis without nasal polyps. J. Allergy Clin. Immunol., 2021, Vol. 147, no. 4, pp. 1306-1317.
8. Meng J., Zhou P., Liu Y., Liu F., Yi X., Liu S., Holtappels G., Bachert C., Zhang N. The development of nasal polyp disease involves early nasal mucosal inflammation and remodelling. PLoS ONE, 2013, Vol. 8, no. 12, e82373. doi: 10.1371/journal.pone.0082373.
9. Mueller S.K., Wendler O., Nocera A., Grundtner P., Schlegel P., Agaimy A., Iro H., Bleier B.S. Escalation in mucus cystatin 2, pappalysin-A, and periostin levels over time predict need for recurrent surgery in chronic rhinosinusitis with nasal polyps. Int. Forum Allergy Rhinol., 2019, Vol. 9, no. 10, pp. 1212-1219.
10. Nagarkar D.R., Poposki J.A., Tan B.K., Comeau M.R., Peters A.T., Hulse K.E., Suh L.A., Norton J., Harris K.E., Grammer L.C., Chandra R.K., Conley D.B., Kern R.C., Schleimer R.P., Kato A. Thymic stromal lymphopoietin activity is increased in nasal polyps of patients with chronic rhinosinusitis. J. Allergy Clin. Immunol., 2013, Vol. 132, no. 3, pp. 593-600.
11. Park S.K., Jin Y.D., Park Y.K., Yeon S.H., Xu J., Han R.N., Rha K.S., Kim Y.M. IL-25-induced activation of nasal fibroblast and its association with the remodeling of chronic rhinosinusitis with nasal polyposis. PLoS ONE, 2017, Vol. 12, no. 8, e0181806. doi: 10.1371/journal.pone.0181806.
12. Soler Z.M., Yoo F., Schlosser R.J., Mulligan J., Ramakrishnan V.R., Beswick D.M., Alt J.A., Mattos J.L., Payne S.C., Storck K.A., Smith T.L. Correlation of mucus inflammatory proteins and olfaction in chronic rhinosinusitis. Int. Forum Allergy Rhinol., 2020, Vol. 10, no. 3, pp. 343-355.
13. Soyka M.B., Wawrzyniak P., Eiwegger T., Holzmann D., Treis A., Wanke K., Kast J.I., Akdis C.A. Efective epithelial barrier in chronic rhinosinusitis: The regulation of tight junctions by IFN-gamma and IL-4. J. Allergy Clin. Immunol., 2012, Vol. 130, no. 5, pp. 1087-1096.e10.
14. Wise S.K., Laury A.M., Katz E.H., Den Beste K.A., Parkos C.A., Nusrat A. Interleukin-4 and interleukin-13 compromise the sinonasal epithelial barrier and perturb intercellular junction protein expression. Int. Forum Allergy Rhinol., 2014, Vol. 4, no. 5, pp. 361-370.
15. Yan B., Lou H., Wang Y., Li Y., Meng Y., Qi S., Wang M., Xiao L., Wang C., Zhang L. Epithelium-derived cystatin SN enhances eosinophil activation and infiltration through IL-5 in patients with chronic rhinosinusitis with nasal polyps. J. Allergy Clin. Immunol., 2019, Vol. 144, no. 2, pp. 455-469.
Review
For citations:
Lazareva A.M., Smirnova O.V. Features of the cytokine profile repolarization in the patients with chronic rhinosinusitis and comorbid conditions. Medical Immunology (Russia). 2026;28(1):65-72. (In Russ.) https://doi.org/10.15789/1563-0625-FOT-3259
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