IMPACT OF HYPERBARIC OXYGEN THERAPY ON PLACENTAL FUNCTIONAL ACTIVITY
DOI:
https://doi.org/10.11603/24116-4944.2026.1.16367Keywords:
immunogram, placenta, hyperbaric oxygenation, HLA-G, miscarriageAbstract
The aim of the study – to determine alterations in immunological parameters in placental insufficiency and to assess the effectiveness of hyperbaric oxygenation courses as part of complex therapy aimed at correcting placental protective function.
Materials and Methods. The study included 105 pregnant women at 16–22 weeks of gestation, divided into three groups: 40 with uncomplicated pregnancy, 35 with placental insufficiency receiving standard therapy, and 30 with placental insufficiency additionally treated with hyperbaric oxygenation. Immunological parameters were assessed in all participants.
Results and Discussion. Total lymphocyte and T-helper counts were reduced compared to physiological pregnancy, whereas CD8+ and NK cells were elevated. CD72+ levels did not differ significantly but showed an increasing trend. B lymphocytes and hematocrit were higher in placental pathology, while HLA-G concentration in peripheral blood was reduced versus controls. After treatment, the total number of T lymphocytes increased more significantly in group IIb. In groups IIa and IIb, CD4+ lymphocyte levels increased from (41.33±0.15) to (42.9±0.13) % and from (39.91±0.14) to (43.50±0.13) %, respectively (p<0.05). The proportion of CD8+ decreased more markedly with hyperbaric oxygenation: from (31.72±2.33) to (22.33±1.51) % (p<0.05). CD16+ lymphocytes also decreased, especially in group IIb, to (12.91±1.13) % (p<0.05). Active B lymphocytes declined to (7.00±0.41) % (p<0.05), while changes in mature B cells were not statistically significant. Hematocrit decreased in both groups, more substantially after oxygen therapy. An increase in serum HLA-G was observed: after standard therapy – from (0.026±0.004) to (0.089±0.011) mg/ml, and after oxygen therapy – from (0.029±0.005) to (0.091±0.009) mg/ml (p<0.05). These findings confirm the higher effectiveness of complex therapy including hyperbaric oxygenation.
Conclusions. Immunogram parameters may be used as an additional marker in the diagnosis of placental insufficiency. Incorporating oxygen therapy courses into complex treatment improves the correction of placental protective function.
References
1. Ding, J., Maxwell, A., Adzibolosu, N., Hu, A., You, Y., Liao, A., & Mor, G. (2022). Mechanisms of immune regulation by the placenta: Role of type I interferon and interferon-stimulated genes signaling during pregnancy. Immunological Reviews, 308(1), 9–24. https://doi.org/10.1111/imr.13077
2. Warning, J. C., McCracken, S. A., & Morris, J. M. (2011). A balancing act: Mechanisms by which the fetus avoids rejection by the maternal immune system. Reproduction, 141(6), 715–724. https://doi.org/10.1530/REP-10-0360
3. Panov, V., & Duka, Y. (2023). Osoblyvosti funktsionuvannia imunolohichnoi tolerantnosti pid chas vahitnosti (ohliad literatury) [Peculiarities of functioning of immunological tolerance during pregnancy (literature review)]. Ukrainian Journal of Perinatology and Pediatrics, 1(93), 76–86. doi: 10.15574/PP.2023.93.76.
4. Moldenhauer, L. M., Hull, M. L., Foyle, K. L., McCormack, C. D., & Robertson, S. A. (2022). Immune-metabolic interactions and T cell tolerance in pregnancy. Journal of Immunology, 209(8), 1426–1436. https://doi.org/10.4049/jimmunol.2200362
5. Zhou, J., Yan, P., Ma, W., & Li, J. (2025). Cytokine modulation and immunoregulation of uterine NK cells in pregnancy disorders. Cytokine & Growth Factor Reviews, 81, Article 101007. https://doi.org/10.1016/j.cytogfr.2024.11.007
6. Sotiros, A., Thornhill, D., Post, M. D., Winn, V. D., & Armstrong, J. (2021). Inflammatory cytokines, placental pathology, and neurological outcomes in infants born to preterm preeclamptic mothers. PLOS ONE, 16(11), e0260094. https://doi.org/10.1371/journal.pone.0260094
7. Tantengco, O. A. G., Richardson, L., Lee, A., Kammala, A., Silva, M. C., Shahin, H., et al. (2021). Histocompatibility antigen, class I, G (HLA-G)'s role during pregnancy and parturition: A systematic review of the literature. Life, 11(10), 1061. https://doi.org/10.3390/life11101061
8. Klemetti, M. M., Pettersson, A. B. V., Ahmad Khan, A., Ermini, L., Porter, T. R., Litvack, M. L., et al. (2024). Lipid profile of circulating placental extracellular vesicles during pregnancy identifies foetal growth restriction risk. Journal of Extracellular Vesicles, 13(2), e12413. https://doi.org/10.1002/jev2.12413
9. Huang, E. T., Mansouri, J., Murad, M. H., Joseph, W. S., Strauss, M. B., Tettelbach, W., et al. (2015). A clinical practice guideline for the use of hyperbaric oxygen therapy in the treatment of diabetic foot ulcers. Undersea & Hyperbaric Medicine, 42(3), 205–247.
10. Moura, N. S., Gomes, M. L. S., Rodrigues, I. R., Rolnik, D. L., Costa, F. S., & Oriá, M. O. B. (2020). Clinical procedures for the prevention of preeclampsia in pregnant women: A systematic review. Revista Brasileira de Ginecologia e Obstetrícia, 42(10), 659–668. https://doi.org/10.1055/s-0040-1714135
11. Skrypnyk, V. V., & Tsysar, Yu. V. (2023). Placental insufficiency (literature review). In Proceedings of the 2nd International Scientific and Practical Conference "Global Science: Prospects and Innovations" (pp. 172–179). Liverpool, United Kingdom: Cognum Publishing House.
12. Wardinger, J. E., & Ambati, S. (2022). Placental insufficiency. In StatPearls. Treasure Island (FL): StatPearls Publishing.
13. Rudyuk, O. H., & Yasnikovska, S. M. (2023). The use of nitric oxide donors in the treatment of placental dysfunction. In Proceedings of the 1st International Scientific and Practical Conference "Modern Problems of Science, Education and Society" (pp. 144–148). Kyiv, Ukraine.
14. Peng, X., Chinwe Oluchi-Amaka, I., Kwak-Kim, J., & Yang, X. (2025). A comprehensive review of the roles of T-cell immunity in preeclampsia. Frontiers in Immunology, 16, 1476123. https://doi.org/10.3389/fimmu.2025.1476123
15. Liao, J., Li, Y., Li, X., Su, X., Peng, J., Xiao, N., et al. (2022). Blood CD4+CD25+ regulatory T cells constitute a potential predictive marker of subsequent miscarriage in unexplained recurrent pregnancy loss. International Immunopharmacology, 110, 108960. https://doi.org/10.1016/j.intimp.2022.108960
16. Hardardottir, L., Bazzano, M. V., Glau, L., Gattinoni, L., Köninger, A., Tolosa, E., & Solano, M. E. (2021). The new old CD8+ T cells in the immune paradox of pregnancy. Frontiers in Immunology, 12, 765730. https://doi.org/10.3389/fimmu.2021.765730
17. Cavalcante, M. B., da Silva, P. H. A., Carvalho, T. R., Sampaio, O. G. M., Câmara, F. E. A., Cavalcante, C. T. M. B., et al. (2023). Peripheral blood natural killer cell cytotoxicity in recurrent miscarriage: A systematic review and meta-analysis. Journal of Reproductive Immunology, 158, 103956. https://doi.org/10.1016/j.jri.2023.103956
18. Weng, J., Couture, C., & Girard, S. (2023). Innate and adaptive immune systems in physiological and pathological pregnancy. Biology, 12(3), 402. https://doi.org/10.3390/biology12030402
19. Pan, J., Tian, X., Huang, H., & Zhong, N. (2020). Proteomic study of fetal membrane: Inflammation-triggered proteolysis of extracellular matrix may present a pathogenic pathway for spontaneous preterm birth. Frontiers in Physiology, 11, 800. https://doi.org/10.3389/fphys.2020.00800
20. Steinborn, A., Schmitt, E., Kisielewicz, A., Rechenberg, S., Seissler, N., Mahnke, K., et al. (2012). Pregnancy-associated diseases are characterized by the composition of the systemic regulatory T-cell (Treg) pool with distinct subsets of Tregs. Clinical and Experimental Immunology, 167(1), 84–98. https://doi.org/10.1111/j.1365-2249.2011.04493.x
21. Lu, Z. M., Goldenberg, R. L., Cliver, S. P., Cutter, G., & Blankson, M. (1991). The relationship between maternal hematocrit and pregnancy outcome. Obstetrics and gynecology, 77(2), 190–194. https://doi.org/10.1097/00006250-199102000-00005
22. Yie, S. M., Li, L. H., Li, Y. M., & Librach, C. (2004). HLA-G protein concentrations in maternal serum and placental tissue are decreased in preeclampsia. American Journal of Obstetrics and Gynecology, 191(2), 525–529. https://doi.org/10.1016/j.ajog.2004.01.033
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