Disease phenotype-driven alterations in cellular and humoral immunity during chronic rhinosinusitis
- Authors: Smirnova O.V.1, Sinyakov A.A.1
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Affiliations:
- Federal Research Center “Krasnoyarsk Science Center” of the Siberian Branch of the Russian Academy of Sciences, Scientific Research Institute of Medical Problems of the North
- Issue: Vol 14, No 6 (2024)
- Pages: 1097-1103
- Section: ORIGINAL ARTICLES
- URL: https://journals.rcsi.science/2220-7619/article/view/283030
- DOI: https://doi.org/10.15789/2220-7619-DPA-17705
- ID: 283030
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Abstract
Human nasal cavity and paranasal sinuses play a crucial role in the physiological processes in vivo that accounts for the constant attention of doctors of many specialties to the state and pathological changes in the respiratory compartments noted above. Rhinosinusites hold one of the leading places in the pattern of inflammatory pathology of the paranasal sinuses, regardless of patient age, the climatic zone of residence and living style level. Chronic vs acute rhinosinusitis is less widespread but considered to be the most common chronic disease. This pathology develops on average in 5% population, and CRS incidence increased more than by 2-fold over the last 10 years. In the pattern of subjects admitted to otorhinolaryngological hospitals, CRS comprises 25–30% that progressively elevates by mean 1–2% every year. The aim of the study was to evaluate disease phenotype-driven alterations in cellular and humoral immunity in patients with chronic rhinosinusitis. 91 patients with chronic rhinosinusitis were selected. For the study of cellular immunity, a flow cytometry was used with “Cytomics FC500” (Beckman Coulter, USA) and monoclonal antibodies CD3+, CD4+, CD8+, CD16+, CD19+ (Beckman Coulter, USA). To measure the levels of blood serum immunoglobulins of various classes (A, M, E, G), an enzyme-linked immunosorbent analysis (ELISA) was used. Statistical data processing was carried out using Statistica for Windows 8.0 application programs (StatSoftink, USA, 2008). The study revealed changes in the cellular and humoral links of immunity in chronic rhinosinusitis coupled to distinct disease phenotypes: with chronic allergic rhinosinusitis — 5; in chronic polypose rhinosinusitis — 4; in chronic infectious rhinosinusitis — 3; in chronic hyperplastic rhinosinusitis — 4. With allergic chronic rhinosinusitis, it was linked to higher absolute B-lymphocyte count, hypergammaglobulinemia E and a decrease in 3 indices of relative synthesis were revealed. Polypose chronic rhinosinusitis was associated with elevated in absolute B-lymphocyte level, hypergammaglobulinemia E and decrease in 2 indices of relative synthesis, whereas infectious chronic rhinosinusitis was accompanied by increased B-lymphocyte level and decrease in 2 indices of relative synthesis. Hyperplastic chronic rhinosinusitis patients had higher in absolute T- and B-lymphocyte count and a decreased absolute cytotoxic T-lymphocyte level along with 2 indices of relative synthesis.
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##article.viewOnOriginalSite##About the authors
Olga V. Smirnova
Federal Research Center “Krasnoyarsk Science Center” of the Siberian Branch of the Russian Academy of Sciences, Scientific Research Institute of Medical Problems of the North
Author for correspondence.
Email: ovsmirnova71@mail.ru
DSc (Medicine), Professor, Head of the Laboratory of Clinical Pathophysiology
Russian Federation, KrasnoyarskA. A. Sinyakov
Federal Research Center “Krasnoyarsk Science Center” of the Siberian Branch of the Russian Academy of Sciences, Scientific Research Institute of Medical Problems of the North
Email: ovsmirnova71@mail.ru
PhD (Biology), Senior Researcher, Laboratory of Clinical Pathophysiology
Russian Federation, KrasnoyarskReferences
- Eгоров В.И., Савлевич Е.Л. Место врожденного иммунитета в развитии хронического риносинусита и перспективы тактики консервативного лечения // Альманах клинической медицины. 2016. Т. 44, № 7. С. 850–856. [Egorov V.I., Savlevich E.L. The role of innate immunity in the development of chronic rhinosinusitis and perspectives of its conservative management. Al’manakh klinicheskoi meditsiny = Almanac of Clinical Medicine, 2016, vol. 44, no. 7, pp. 850–856. (In Russ.)] doi: 10.18786/2072-0505-2016-44-7-850-856
- Захарова Г.П. Характеристика ультраструктурных особенностей слизистой оболочки верхнечелюстной пазухи при хроническом риносинусите // Новости оториноларингологии и логопатологии. 2002. Т. 3. С. 25–29. [Zaharova G.P. Characterisation of ultrastructural features of the maxillary sinus mucosa in chronic rhinosinusitis. Novosti otorinolaringologii i logopatologii = Otorhinolaryngology and Speech Pathology News, 2002, vol. 3, pp. 25–29. (In Russ.)]
- Крюков А.И., Студеный М.Е., Артемьев М.Е., Чумаков П.Л., Рынков Д.А., Горин Д.С. Лечение пациентов с риносинуситами: возможности консервативного и оперативного воздействия // Медицинский совет. 2012. Т. 11. С. 92–96. [Kryukov A.I., Studenyj M.E., Artem’ev M.E., Chumakov P.L., Rynkov D.A., Gorin D.S. Treatment of patients with rhinosinusitis: conservative and surgical options. Meditsinskiy sovet = Medical Council, 2012, vol. 11, pp. 92–96. (In Russ.)]
- Шадыев Т.Х., Изотова Г.Н., Сединкин А.А. Острый синусит // Русский медицинский журнал. 2013. Т. 11. С. 567–574 [Shadyev T.H., Izotova G.N., Sedinkin A.A. Acute sinusitis. Russkii meditsinskii zhurnal = Russian Medical Journal, 2013, vol. 11, pp. 567–574. (In Russ.)]
- Anand V.K. Epidemiology and economic impact of rhinosinusitis. Ann. Otol. Rhinol. Laryngol. Suppl., 2004, vol. 193, pp. 3–5. doi: 10.1177/00034894041130s502
- Benninger M.S., Ferguson B.J., Hadley J.A. Hamilos D.L., Jacobs M., Kennedy D.W., Lanza D.C., Marple B.F., Osguthorpe J.D., Stankiewicz J.A., Anon J., Denneny J., Emanuel I., Levine H. Adult chronic rhinosinusitis: definitions, diagnosis, epidemiology, and pathophysiology. Otolaryngol. Head Neck Surg., 2003, vol. 129 (3 Suppl), pp. S1–S32. doi: 10.1016/s0194-5998(03)01397-4
- Epple H.J., Allers K., Tröger H., Kühl A., Erben U., Fromm M., Zeitz M., Loddenkemper C., Schulzke J.D., Schneider T. Acute HIV infection induces mucosal infiltration with CD4+ and CD8+ T cells, epithelial apoptosis, and a mucosal barrier defect. Gastroenterology, 2010, vol. 139, no. 4, pp. 1289–1300. doi: 10.1053/j.gastro.2010.06.065
- Fokkens W.J., Lund V.J., Mullol J., Bachert C., Alobid I., Baroody F., Cohen N., Cervin A., Douglas R., Gevaert P., Georgalas C., Goossens H., Harvey R., Hellings P., Hopkins C., Jones N., Joos G., Kalogjera L., Kern B., Kowalski M., Price D., Riechelmann H., Schlosser R., Senior B., Thomas M., Toskala E., Voegels R., Wang de Y., Wormald P.J. European position paper on rhinosinusitis and nasal polyps 2012. Rhinology, 2012, vol. 50, no. 1, pp. 1–12. doi: 10.4193/Rhino12.000
- Johnson J.T., Yu V.L. Infection diseases and antimicrobial therapy of the ears, nose and throat. Philadelphia US: Saunders, 1997. 641 p.
- Lee J.T., Kennedy D.W., Palmer J.N., Feldman M., Chiu. A.G. The incidence of concurrent osteitis in patients with chronic rhinosinusitis: a clinicopathological study. Am. J. Rhinol., 2006, vol. 20, no. 3, pp. 278–282. doi: 10.2500/ajr.2006.20.2857
- Ooi E.H., Wormald P.J., Tan L.W. Innate immunity in the paranasal sinuses: a review of nasal host defenses. Am. J. Rhinol., 2008, vol. 22, no. 1, pp. 13–19. doi: 10.2500/ajr.2008.22.3127
- Pankey G.A., Gross C.W., Mendelson M.G. Contemporary diagnosis and management of sinusitis. Pennsylvania: Handbooks in Health Care Company, 1997. 160 p.
- Tan B.K., Li Q.Z., Suh L., Kato A., Conley D.B., Chandra R.K., Zhou J., Norton J., Carter R., Hinchcliff M., Harris K., Peters A., Grammer L.C., Kern R.C., Mohan C., Schleimer R.P. Evidence for intranasal antinuclear autoantibodies in patients with chronic rhinosinusitis with nasal polyps. J. Allergy Clin. Immunol., 2011, vol. 128, no. 6, pp. 1198–1206. doi: 10.1016/j.jaci.2011.08.037
- Van Crombruggen K., Zhang N., Gevaert P., Tomassen P., Bachert C. Pathogenesis of chronic rhinosinusitis: inflammation. J. Allergy Clin. Immunol., 2011, vol. 128, no. 4, pp. 728–732. doi: 10.1016/j. jaci.2011.07.049
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