ISSN 2415-3060 (print), ISSN 2522-4972 (online)
  • 7 of 46
Up
JMBS 2022, 7(1): 62–67
https://doi.org/10.26693/jmbs07.01.062
Experimental Medicine and Morphology

Influence of Cell Therapy on the Dynamics of Inflammatory Markers in Blood of Rats with Adjuvant Arthritis

Vvedenskyi D. B. 1,2, Volkova N. О. 1, Yukhta M. S. 1, Sokil L. V. 1, Goltsev A. M. 1
Abstract

The purpose of the study was to investigate the dynamics of inflammation in blood of the rats with adjuvant arthritis under the conditions of generalized and local administration of cryopreserved multipotent mesenchymal stromal cells from adipose and cartilage tissues. Materials and methods. A model of adjuvant arthritis in male rats was induced by subplantar administration of Freund’s complete adjuvant. On the 7th day of modeling, experimental animals were administered: control group – saline; experimental group 1 and 2 – cryopreserved multipotent mesenchymal stromal cells from adipose or cartilaginous tissue locally; experimental group 3 and 4 – cryopreserved multipotent mesenchymal stromal cells from adipose or cartilaginous tissue generalized. Groups of intact animals served as control. On days 14, 21 and 28 erythrocyte sedimentation rate was determined in blood, and content of total protein, C-reactive protein and rheumatoid factor were measured in serum. Results and discussion. In the control group of animals, the inflammatory process was pronounced, as evidenced by a significant increase in the studied parameters throughout the observation period. The use of cryopreserved multipotent mesenchymal stromal cells from adipose and cartilaginous tissues led to the restoration of the total protein content and erythrocyte sedimentation rate on the 28th day of observation, as well as positive dynamics in the level of C-reactive protein and rheumatoid factor. Generalized administration of cells had a more pronounced therapeutic effect compared to the animals with local one. A comparative assessment of the use of cryopreserved multipotent mesenchymal stromal cells from adipose and cartilaginous tissues showed the absence of significant changes in the studied parameters both with studied ways of cell administration. These data can be used to justify and develop methods of treating arthritis in clinical practice. But important issue that needs further research is the determination of cell immunity in the animals with adjuvant arthritis and treatment of cryopreserved multipotent mesenchymal stromal cells from adipose and cartilage tissues. Conclusion. Cell therapy with the use of cryopreserved multipotent mesenchymal stromal cells from the investigated sources provided by both local and generalized administration to animals with adjuvant arthritis has a modulating effect on the course of inflammation

Keywords: adjuvant arthritis, cryopreserved multipotent mesenchymal stromal cells, cell therapy, markers of inflammation, blood

Full text: PDF (Ukr) 258K

References
  1. Bullock J, Rizvi S, Saleh AM, Ahmed SS, Do DP, Ansari RA, et al. Rheumatoid arthritis: A brief overview of the treatment. Med Princ Pract. 2018;27(6):501-507. PMID: 30173215. https://doi.org/10.1159/000493390
  2. To K, Khan W. Mesenchymal Stem cell transplantation in rheumatoid arthritis. In: Pham P, Ed. Stem cells in clinical applications. Springer: Cham; 2019. https://doi.org/10.1007/978-3-030-23421-8_4
  3. Freitag J, Bates D, Boyd R, Shah K, Barnard A, Huguenin L, et al. Mesenchymal stem cell therapy in the treatment of osteoarthritis: reparative pathways, safety and efficacy - a review. BMC Musculoskelet Disord. 2016;17(1):1-13. PMID: 27229856. PMCID: PMC4880954. https://doi.org/10.1186/s12891-016-1085-9
  4. Fu Y, Karbaat L, Wu L, Leijten J, Both SK, Karperien M. Trophic effects of mesenchymal stem cells in tissue regeneration. Tissue Eng Part B Rev. 2017;23(6):515-528. PMID: 28490258. https://doi.org/10.1089/ten.TEB.2016.0365
  5. Volkovа NA, Yukhta MS, Goltsev AN. Morphological and functional characteristics of cryopreserved multipotent mesenchymal stromal cells from bone marrow, adipose tissue and tendons. Cell and Organ Transplantology. 2016;4(2):200-205. https://doi.org/10.22494/cot.v4i2.64
  6. Perez L. Acute phase protein response to viral infection and vaccination. Arch Biochem Biophys. 2019;671:196-202. PMID: 31323216. PMCID: PMC7094616. https://doi.org/10.1016/j.abb.2019.07.013
  7. Volkova NА, Yukhta MS, Yurchuk ТА, Ivanova ED, Stepanuk LV, Pavlovich EV, et al. Multipotent mesenchymal stromal cells of bone marrow in therapy of chronic inflammation of the murine ovaries. Biotechnol Acta. 2014;7(5):35-42. https://doi.org/10.15407/biotech7.05.035
  8. Vvedenskyi DB, Volkova N.O, Yukhta MS, Ashukina NO, Goltsev AM. Course correction of adjuvant arthritis with cryopreserved multipotent mesenchymal stromal cells. Regul Mech Biosyst.2021;12(3):545-553. https://doi.org/10.15421/02217
  9. Krampera M, Cosmi L, Angeli R, Pasini A, Liotta F, Andreini A, et al. Role for interferon-gamma in the immunomodulatory activity of human bone marrow mesenchymal stem cells. Stem Cells. 2006;24(2):386-398. PMID: 16123384. https://doi.org/10.1634/stemcells.2005-0008
  10. Tabera S, Perez-Simon JA, Diez-Campelo M. The effect of mesenchymal stem cells on the viability, proliferation and differentiation of B-lymphocytes Haematologica. 2008;93(9):1301-1309. PMID: 18641017. https://doi.org/10.3324/haematol.12857
  11. Zhou Y, Yamamoto Y, Xiao Z, Ochiya T. The immunomodulatory functions of mesenchymal stromal/stem cells mediated via paracrine activity. J Clin Med. 2019;8(7);1025. PMID: 31336889. PMCID: PMC6678920. https://doi.org/10.3390/jcm8071025
  12. Fan XL, Zhang Y, Li X, Fu QL. Mechanisms underlying the protective effects of mesenchymal stem cell-based therapy. Cell Mol Life Sci. 2020;77(14);2771-2794. PMID: 31965214. PMCID: PMC7223321. https://doi.org/10.1007/s00018-020-03454-6