Indicators of immune status in women with different recurrence rates of nonspecific inflammatory diseases of the genital organs

Authors

DOI:

https://doi.org/10.14739/2310-1210.2023.3.269374

Keywords:

deficiency IgE, deficiency NKT cells, relapse, immunologic tests, immunodeficiency

Abstract

Non-specific inflammatory diseases of the female genital organs (NIDFGO) are an important problem of modern gynecology due to their high frequency in the population, the tendency to frequent recurrences, and many cases of resistance to recommended antimicrobial and anti-inflammatory drugs.

Aim: to study indicators of immune status in women with different recurrence rates of NIDFGO and biomarkers of recurrences to improve potential therapeutic approaches and prevent recurrences in the further.

Materials and methods. A prospective single-center controlled non-randomized clinical study was conducted with the participation of 98 adult women. Out of them, 80 patients with NIDFGO had one-year recurrence rate of 1, 2–3, 4 or more events, and 18 age-matched women without NIDFGO were assigned to the control group. Immunogram and hemogram were performed for all study participants using standardized methods. Statistical analysis of the results was performed using IBM SPSS 23 statistical package software.

Results. The mean serum concentration of IgE in patients with frequent relapses was 3 times (p < 0.05) lower than that in women with only one recurrence, 2.6 times (p < 0.05) lower than that in patients with medium recurrence rate, and 3.4 times (p < 0.05) less than in the control. In women with frequent recurrences, the mean relative number of blood NKT cells was 3.5 times (p < 0.05) less than that in patients with only one recurrence, 2.3 times (p < 0.05) less than that in persons with medium recurrence rate, and 3 times (p < 0.05) less as compared to women of the control group.

Conclusions. Selective deficiencies of IgE and NKT cells in women with NIDFGO are factors that lead to a higher frequency of disease exacerbations per year. T he development and clinical approval of immunotherapeutic approaches to compensate for deficiencies of IgE and NKT cells in women with NIDFGO will contribute to the imposition of immune control over the inflammatory process, increase the effectiveness of antimicrobial treatment, resulting in a decrease in the recurrence rate.

Author Biographies

K. I. Davydenko, Bogomolets National Medical University, Kyiv, Ukraine

MD, Postgraduate student, Department of Modern Technologies of Medical Diagnostics and Treatment

D. V. Maltsev, Bogomolets National Medical University, Kyiv, Ukraine

MD, PhD, Head of the Laboratory of Immunology and Molecular Biology, Institute of Experimental and Clinical Medicine

L. V. Natrus, Bogomolets National Medical University, Kyiv, Ukraine

MD, PhD, DSc, Professor, Head of the Department of Modern Technologies of Medical Diagnostics and Treatment

References

Mohankumar, B., Shandil, R. K., Narayanan, S., & Krishnan, U. M. (2022). Vaginosis: Advances in new therapeutic development and microbiome restoration. Microbial pathogenesis, 168, 105606. https://doi.org/10.1016/j.micpath.2022.105606

Davydenko, K. I., Maltsev, D. V., Batman, Yu. A., & Natrus, L. V. (2022). Vyvchennia imunnykh porushen pry nespetsyfichnykh khronichnykh zapalnykh zakhvoriuvanniakh statevykh orhaniv u zhinok [Study of the immune disorders in nonspecific chronic inflammatory diseases of the genital organs]. Fiziologichnyi Zhurnal, 68(3), 68-77. [in Ukrainian]. https://doi.org/10.15407/fz68.03.068

Pate, M. B., Smith, J. K., Chi, D. S., & Krishnaswamy, G. (2010). Regulation and dysregulation of immunoglobulin E: a molecular and clinical perspective. Clinical and molecular allergy : CMA, 8, 3. https://doi.org/10.1186/1476-7961-8-3

Colas, L., Magnan, A., & Brouard, S. (2022). Immunoglobulin E response in health and disease beyond allergic disorders. Allergy, 77(6), 1700-1718. https://doi.org/10.1111/all.15230

Roco, J. A., Mesin, L., Binder, S. C., Nefzger, C., Gonzalez-Figueroa, P., Canete, P. F., Ellyard, J., Shen, Q., Robert, P. A., Cappello, J., Vohra, H., Zhang, Y., Nowosad, C. R., Schiepers, A., Corcoran, L. M., Toellner, K. M., Polo, J. M., Meyer-Hermann, M., Victora, G. D., & Vinuesa, C. G. (2019). Class-Switch Recombination Occurs Infrequently in Germinal Centers. Immunity, 51(2), 337-350.e7. https://doi.org/10.1016/j.immuni.2019.07.001

Kawakami, T., Kasakura, K., Kawakami, Y., & Ando, T. (2022). Immunoglobulin E-Dependent Activation of Immune Cells in Rhinovirus-Induced Asthma Exacerbation. Frontiers in allergy, 3, 835748. https://doi.org/10.3389/falgy.2022.835748

Lim, J., Lin, E. V., Hong, J. Y., Vaidyanathan, B., Erickson, S. A., Annicelli, C., & Medzhitov, R. (2022). Induction of natural IgE by glucocorticoids. The Journal of experimental medicine, 219(10), e20220903. https://doi.org/10.1084/jem.20220903

Magen, E., Schlesinger, M., David, M., Ben-Zion, I., & Vardy, D. (2014). Selective IgE deficiency, immune dysregulation, and autoimmunity. Allergy and asthma proceedings, 35(2), e27-e33. https://doi.org/10.2500/aap.2014.35.3734

García Pavón Osorio, S., López Tiro, J. J., & Gómez Vera, J. (2009). Deficiencia de IgE: un padecimiento olvidado? [IgE deficiency: a forgotten disease?]. Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993), 56(6), 192-197.

Starkl, P., Watzenboeck, M. L., Popov, L. M., Zahalka, S., Hladik, A., Lakovits, K., Radhouani, M., Haschemi, A., Marichal, T., Reber, L. L., Gaudenzio, N., Sibilano, R., Stulik, L., Fontaine, F., Mueller, A. C., Amieva, M. R., Galli, S. J., & Knapp, S. (2020). IgE Effector Mechanisms, in Concert with Mast Cells, Contribute to Acquired Host Defense against Staphylococcusaureus. Immunity, 53(4), 793-804.e9. https://doi.org/10.1016/j.immuni.2020.08.002

Jakwerth, C. A., Ordovas-Montanes, J., Blank, S., Schmidt-Weber, C. B., & Zissler, U. M. (2022). Role of Respiratory Epithelial Cells in Allergic Diseases. Cells, 11(9), 1387. https://doi.org/10.3390/cells11091387

Correa, F. J. S., Andres, M. P., Rocha, T. P., Carvalho, A. E. Z., Aloia, T. P. A., Corpa, M. V. N., Kallas, E. G., Mangueira, C. L. P., Baracat, E. C., Carvalho, K. I., & Abrão, M. S. (2022). Invariant Natural Killer T-cells and their subtypes may play a role in the pathogenesis of endometriosis. Clinics (Sao Paulo, Brazil), 77, 100032. https://doi.org/10.1016/j.clinsp.2022.100032

Wen, X., Zhang, X., Nian, S., Wei, G., Guo, X., Yu, H., Xie, X., Ye, Y., & Yuan, Q. (2021). Title of article: Mucosal-associated invariant T cells in lung diseases. International immunopharmacology, 94, 107485. https://doi.org/10.1016/j.intimp.2021.107485

Chung, B. K., Tsai, K., Allan, L. L., Zheng, D. J., Nie, J. C., Biggs, C. M., Hasan, M. R., Kozak, F. K., van den Elzen, P., Priatel, J. J., & Tan, R. (2013). Innate immune control of EBV-infected B cells by invariant natural killer T cells. Blood, 122(15), 2600-2608. https://doi.org/10.1182/blood-2013-01-480665

Björkström, N. K., Strunz, B., & Ljunggren, H. G. (2022). Natural killer cells in antiviral immunity. Nature reviews. Immunology, 22(2), 112-123. https://doi.org/10.1038/s41577-021-00558-3

Lang, G. A., Shrestha, B., Amadou Amani, S., Shadid, T. M., Ballard, J. D., & Lang, M. L. (2021). α-Galactosylceramide-Reactive NKT Cells Increase IgG1 Class Switch against a Clostridioides difficile Polysaccharide Antigen and Enhance Immunity against a Live Pathogen Challenge. Infection and immunity, 89(11), e0043821. https://doi.org/10.1128/IAI.00438-21

Nogueira-Neto, J., Loures, F. V., Schanoski, A. S., Andrade, D. A. G., Gonzatti, M. B., Costa, T. A., Vivanco, B. C., Xander, P., Rosa, D. S., Calich, V. L. G., & Keller, A. C. (2021). Invariant Natural Killer T Cells as Key Players in Host Resistance against Paracoccidioides brasiliensis. Journal of immunology research, 2021, 6673722. https://doi.org/10.1155/2021/6673722

Hirai, T., Lin, P. Y., Simonetta, F., Maas-Bauer, K., Turkoz, M., Mavers, M., Baker, J., & Negrin, R. S. (2021). Activation of natural killer T cells enhances the function of regulatory T-cell therapy in suppressing murine GVHD. Blood advances, 5(11), 2528-2538. https://doi.org/10.1182/bloodadvances.2020003272

Published

2023-05-31

How to Cite

1.
Davydenko KI, Maltsev DV, Natrus LV. Indicators of immune status in women with different recurrence rates of nonspecific inflammatory diseases of the genital organs. Zaporozhye Medical Journal [Internet]. 2023May31 [cited 2024Dec.26];25(3):248-54. Available from: http://zmj.zsmu.edu.ua/article/view/269374