EFFECT OF LEECH EXTRACT ON LYMPHOCYTES IN THERMAL BURNS
DOI:
https://doi.org/10.58407/bht.1.26.10Keywords:
lymphocytes, blast transformation, thermal burn, leech extract, immunomodulationAbstract
Purpose of the work. The study aimed to evaluate changes in the quantitative composition of lymphocytes and the blast transformation reaction of lymphocytes under spontaneous conditions and concanavalin A stimulation during the healing of a thermal burn, as well as to determine the immunomodulatory effect of the water-salt extract of the medicinal leech (Hirudo verbana).
Methodology. The experimental study was conducted using a thermal burn model. Animals were divided into intact, control (thermal burn without treatment), and experimental groups treated with the water-salt extract of Hirudo verbana. Blood samples were collected on days 3, 7, 14, and 30 after injury. The percentage of lymphocytes and the blast transformation reaction of lymphocytes were assessed under spontaneous conditions and after stimulation with concanavalin A using standard immunological methods. Results were expressed as M ± m, and statistical analysis was performed using Student’s t-test.
Scientific novelty. For the first time, the dynamics of lymphocyte proliferative activity during thermal burn healing under the influence of the water-salt extract of the medicinal leech were quantitatively characterized. It was demonstrated that the extract promotes faster restoration of ConA-induced blast transformation of lymphocytes and prevents prolonged post-burn immunosuppression.
Conclusions. Thermal burn injury caused transient lymphopenia, increased spontaneous blast transformation, and suppression of mitogen-induced lymphocyte proliferation. Application of the water-salt extract of Hirudo verbana reduced the severity of these changes and ensured normalization of both quantitative and functional lymphocyte parameters by day 14 of the experiment. The obtained results confirm the pronounced immunomodulatory potential of the medicinal leech extract during reparative processes.
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References
Ali, S. K., & Wunu, A. G. (2025). A review of bioactive molecules in leech saliva and their medical importance. Preprints, 2025041943. https://doi.org/10.20944/preprints202504.1943.v1
Amani, L., Motamed, N., Mirabzadeh, A. M., Dehghan, S. M., Malek, M., & Shamsa, F. (2021). Semi-solid product of medicinal leech enhances wound healing in rats. Jundishapur Journal of Natural Pharmaceutical Products, 16(4), e113910. https://doi.org/10.5812/jjnpp.113910
Aminov, R. (2023). The influence of the water-salt extract of the medicinal leech Hirudo verbana Carena, 1820 on the general course of embryogenesis in rats after intraperitoneal administration. Studia Biologica, 17(2), 85–94. https://doi.org/10.30970/sbi.1702.713
Aminov, R., & Aminova, A. (2021). Indirect effect of substances of the hemophagous parasite Hirudo verbana on the immune system of the host rats. Annals of Parasitology, 67(4), 603–610. https://doi.org/10.17420/ap6704.376
Aminov, R., Frolov, A., & Aminova, A. (2022). The effect of the biologically complex of a medical leech active substances on the immunosuppressive state of rats. Jordan Journal of Biological Sciences, 15(2), 257–261. https://doi.org/10.54319/jjbs/150213
Aminov, R. F., & Aminova, A. S. (2025). Excisional wound morphological characteristics under the influence of medicinal leech biologically active substances. Innovative Biosystems and Bioengineering, 9(3), 3–13. https://doi.org/10.20535/ibb.2025.9.3.322167
Aminov, R. F., & Aminova, A. S. (2025). Method for obtaining a water-salt extract of the medicinal leech. Ukrainian Patent No. 161697. Ukrainian National Office for Intellectual Property and Innovations. (in Ukrainian)
Амінов Р. Ф., Амінова А. С. Спосіб отримання водно-сольового екстракту медичної п’явки. Патент України № 161697. Український національний офіс інтелектуальної власності та інновацій.
Ayhan, H., Sevin, S., Karaaslan, S., & Ayaz, F. (2025). Immunomodulatory effects of medicinal leech saliva extract on in vitro activated macrophages. Immunologic Research, 73(1), 9–16. https://doi.org/10.1007/s12026-024-09575-5
Burgess, M., Valdera, F., Varon, D., Kankuri, E., & Nuutila, K. (2022). The immune and regenerative response to burn injury. Cells, 11(19), 3073. https://doi.org/10.3390/cells11193073
Dincer, H. A., Ozsahin, A. G., & Bayraktaroglu, T. (2025). Pan immune inflammation value as a novel marker in burn injury prognostics. Medicina (Kaunas), 61(9), 1705. https://doi.org/10.3390/medicina61091705
Jiang, L., Zhu, Y., Zhang, W., Xie, S., Wu, M., Xu, D., Wang, S., Xian, S., Lu, J., Tong, X., Liu, Y., Huang, J., Guo, X., Gu, M., Jin, S., Ma, Y., Huang, R., Ji, S., & Xia, Z. (2024). Scholarly knowledge fundamentals and dynamic research hotspots in the field of burns and immunology: A bibliometric analysis. Burns. 50(9), 107220. https://doi.org/10.1016/j.burns.2024.07.024
Korkmaz, H. I., Flokstra, G., Waasdorp, M., Pijpe, A., Papendorp, S. G., de Jong, E., Rustemeyer, T., Gibbs, S., & van Zuijlen, P. P. M. (2023). The complexity of the post-burn immune response. Cells, 12(3), 345. https://doi.org/10.3390/cells12030345
Mulder, P. P. G., Vlig, M., Fasse, E., Stoop, M. M., Pijpe, A., van Zuijlen, P. P. M., Joosten, I., Boekema, B. K. H. L., & Koenen, H. J. P. M. (2022). Burn injured skin is marked by a prolonged local acute immune response. Frontiers in Immunology, 13, 1034420. https://doi.org/10.3389/fimmu.2022.1034420
Nourigheimasi, S., Amiresmaili, M., & Hosseinpour, M. (2024). Association of inflammatory biomarkers with overall survival in burn patients. BMC Emergency Medicine, 24, 88. https://doi.org/10.1186/s12873-024-00988-x
Osuka, A., Shigeno, A., Matsuura, H., Onishi, S., & Yoneda, K. (2024). Systemic immune response of burns from the acute to chronic phase. Journal of Burn Care & Research, 11(1), e976. https://doi.org/10.1002/ams2.976
Rasheed, B. N. (2023). Lymphocytic immune response of children after thermal burn injury. History of Medicine, 9(1), 898–901. https://doi.org/10.17720/2409-5834.v9.1.2023.102
Simon-Molas, H., Vallvé-Martínez, X., Caldera-Quevedo, I., Fontova, P., Arnedo-Pac, C., Vidal-Alabró, A., Castaño, E., Navarro-Sabaté, À., Lloberas, N., Bartrons, R., & Manzano, A. (2021). TP53 induced glycolysis and apoptosis regulator (TIGAR) is upregulated in lymphocytes stimulated with concanavalin A. International Journal of Molecular Sciences, 22(14), 7436. https://doi.org/10.3390/ijms22147436
Ünal, K., Erol, M. E., & Ayhan, H. (2023). Literature review on the effectiveness of medicinal leech therapy in wound healing. Ankara Medical Journal, (1), 151–164. https://doi.org/10.5505/amj.2023.20280
Bilden, A., Sabancılar, İ., Yalçın Azarkan, S., Karadağlı, K., Kaya, S., Kahraman, M., & Çiçek, M. (2025). Investigating the Therapeutic Potential of Crude Leech Saliva Based on Its Anticancer, Antioxidant, and Anti-Inflammatory Effects. Current Issues in Molecular Biology, 47(5), 328. https://doi.org/10.3390/cimb47050328
Zakian, A., Ahmadi, H. A., Keleshteri, M. H., Madani, A., Tehrani-Sharif, M., & Rezaie, A. (2022). Study on the effect of medicinal leech therapy (Hirudo medicinalis) on full-thickness excisional wound healing in an animal model. Research in Veterinary Science, 153, 153–168. https://doi.org/10.1016/j.rvsc.2022.10.015
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