THE EFFECT OF CIA ON SERUM IgA LEVELS IN WISTAR RATS

Authors

  • Mire Spasov Faculty of Medical Science, University „Goce Delcev“- Stip, Republic of North Macedonia

Keywords:

RA, CIA, IgA, immune system, rat

Abstract

Rheumatoid arthritis is a chronic, evolving inflammatory disease with joint destruction and systemic manifestations, which begins gradually, and usually first affects the metatarsophalangeal and radiocarpal joints. The body's immune system creates antibodies to defend against bacteria, viruses and other microorganisms, while in autoimmune diseases the immune system reacts with its antibodies against the cells of its own tissue. The etiology of RA has a genetic and epigenetic history. It is assumed that some genetic factors, infectious diseases, and mostly viral infections are the reason for the appearance of the disease. It has been proven that it is about activating the patient's immune system in such a way that the own cells are recognized as foreign, which results in an autoimmune response. The process begins when lymphocytes as immune cells are activated and produce cytokines as chemical messengers. The subject of our interest in this study was to experimentally monitor the level of IgA after RA induced by collagen type-II in two experimental periods of treatment, at one and two months, compared to the control groups of both sexes of experimental animals. For this purpose, we used eight-week-old Wistar rats, raised in standard conditions at a temperature of 20°C, with food and water - ad libitum. They were divided into four groups; group of control males, control females, treated males and treated females. We applied the prepared collagen according to a standard protocol and purified form in an amount of 100 μl collagen solution and 20 μl physiological solution in the right hind joint of each treated animal. The examination of the IgA level was performed in both periods after immunization by the method of column chromatography on the Dimension RL Max device from the manufacturer Siemens, according to a defined work procedure. We finally calculated the content of immunoglobulins according to the obtained absorbance at 280 nm and the total volume of the eluate. The obtained values for IgA show that regardless of gender in the treated experimental groups there are no significant statistical changes for this parameter, while, for example, in the treated male group on the thirtieth and on the sixtieth day of the experiment CIA has almost no effect on the level of IgA in comparison with the control group of male animals. A result that stands out is the increase in the level of IgA on the 60th day of treatment in the female arthrosis group, compared to the control group by 30%. The obtained results lead to the conclusion that CIA type-II has the effect of a statistically insignificant decrease in the level of IgA in the serum at the end of the experimental period, i.e. on the 60th day in arthritic male animals compared to the control, while in the same period in female animals non-significant increase in IgA value compared to the control group.

References

Arnett, F.C. (2021). The American Rheumatism Association 1987 Revised Criteria for the Classification of Rheumatoid Arthritis Rheum 31:315.

Cooke, A., Zaccone, P., Raine, T., Phillips, J.M., Dunne, D.W. (2018). Infection and autoimmunity: Are we winning the war, only to lose the peace? Trends in parasitology. 20(7): 316-321.

Davidson, D., Blanc, A., Filion, D., Wang, H., Plut, P., Pfeffer, G., Buschmann, M.D., Henderson, J.E. (2020). Fibroblast growth factor (FGF) 18 signals through FGF receptor 3 to promote chondrogenesis. In: The Journal of biological chemistry. Band 280, S. 20509–20515.

Girbal-Neuhauser, E., Durieux, J.J., Arnaud, M., et al. (2019). The epitopes targeted by the rheumatoid arthritis-associated antifilaggrin auto-antibodies are posttranslationally generated on various sites of (pro) filaggrin by deimination of arginine re- sidues. J Immunol; 162: 585-594.

Hammond, A., Prior, Y., Cotterill, S., Sutton, C., Camacho, E., Heal, C., Adams, J., Hough, Y., O'Neill, TW., Firth, J. (2021). BMC Musculoskelet Disord. 22(1):47. doi: 10.1186/s12891-020-03917-8. PMID: 33419426 Free PMC article. Clinical Trial.

Hammond, A., Prior, Y., Adams, J., Firth, J., O'Neill, T., Hough, Y. (2023). Musculoskeletal Care. 21(2):405-416. doi: 10.1002/msc.1709. Epub 2022 Oct 31. PMID: 36317276 Clinical Trial.

Hetland, G. (2011). The Mushroom Agaricus blazei Murill Elicits Medicinal Effects on Tumor, Infection, Allergy, and Inflammation through Its Modulation of Innate Immunity and Amelioration of Th1/Th2 Imbalance and Inflammation. In: Advances in pharmacological sciences.

Ishii, K.J., Uematsu, S., Akira, S. (2006). Toll gates for future immunotherapy (Review). Current Pharmaceutical Design. 12(32): 4135-4142.

Kim, E.Y., Sudini, K., Singh, A.K., Haque, M., Leaman, D., & Khuder, S. (2018). Ursolic acid facilitates apoptosis in rheumatoid arthritis synovial fibroblasts by inducing SP1-mediated Noxa expression and proteasomal degradation of Mcl-1. Feaeb. J. 32, 6174–6185. doi:10.1096/fj.201800425r.

Maeda, Y., & Takeda, K. (2019). “Host-microbiota interactions in rheumatoid arthritis,” Experimental & Molecular Medicine, vol. 51, no. 12, pp. 1–6.

McAlindon, T. (2004). Effectiveness of glucosamine for symptoms of knee osteoarthritis: results from an internet-based randomized double-blind controlled trial. In: Am J Med. 117, S. 643–649.

Moore, E.E., Bendele, A.M., Thompson, D.L., Littau, A., Wag gie, K.S., Reardon, B., Ellsworth, J.L. (2005). Fibroblast growth factor-18 stimulates chondrogenesis and cartilage repair in a rat model of injury-induced osteoarthritis. In: Osteoarthritis and cartilage / OARS, Osteoarthritis Research Society. Band 13, S. 623–631.

Nakamura, R.M. (2020). Progress in the use of biochemical and biological markers for evaluation of rheumatoid arthri- tis. J Clin Lab Anal; 14: 305-313.

Prior, Y., Sutton, C., Cotterill, S., Adams, J., Camacho, E., Arafin, N., Firth, J., O'Neill, T., Hough, Y., Jones, W., Hammond, A. (2017). BMC Musculoskelet Disord. 18(1):224. doi: 10.1186/s12891-017-1583-4. PMID: 28558734 Free PMC article. Clinical Trial.

Saris, D.B. (2008). Characterized Chondrocyte Implantation Results in Better Structural Repair When Treating Symptomatic Cartilage Defects of the Knee in a Randomized Controlled Trial Versus Microfracture. In: Am J Sports Med. 36, S. 235–246.

Sawitzke, A.D., (2008). The effect of glucosamine and/or chondroitin sulfate on the progression of knee osteoarthritis: A report from the glucosamine/chondroitin arthritis intervention trial. In: Arthritis & Rheumatism. 58, 2008, S. 3183–3191.

Schellekens, G.A., Visser, H., de Jong, B.A., et al. (2021). The diagnostic pro- perties of rheumatoid arthritis antibodies recognizing a cyclic citrullinated peptide. Arthritis Rheum; 43: 155- 163.

Usha, P.R., Naidu, P.U.R. (2004). Randomised, Double-Blind, Parallel, Placebo-Controlled Study of Oral Glucosamine, Methylsulfonylmethane and their Combination in Osteoarthritis. 24, str. 353–363.

Van Boekel, M.A.M., Vossenaar, E.R., Van den Hoogen, F.H.J., van Venrooij, W.J. (2021). Autoantibody systems in rheumatoid arthritis: specificity, sensitivity and diagnostic value. Arthritis Res; 4: 87-93.

Verhoeven, F., Totoson, P., Maguin-Gaté, K., Prigent-Tessier, A., & Marie, C., Wendling, D., et al. (2017). Glucocorticoids improve endothelial function in rheumatoid arthritis: a study in rats with adjuvant-induced arthritis. Clin Exp Immunol. 2017; 188: 208–18. pmid:28152574.

Xu, K., Ren, X., Ju, B., Aihaiti, Y., Cai, Y., Zhang, Y. (2020). Clinical markers combined with HMGB1 polymorphisms to predict efficacy of conventional DMARDs in rheumatoid arthritis patients. Clin Immunol. 221:108592.

Yang, F., Qian, E., & Zhang, M. (2020). “ishen Tongluo formula ameliorates collagen-induced arthritis in mice by modulation of Th17/Treg balance,” Journal of Ethnopharmacology, vol. 250, p. 112428.

Downloads

Published

2023-09-30

How to Cite

Spasov, M. (2023). THE EFFECT OF CIA ON SERUM IgA LEVELS IN WISTAR RATS. KNOWLEDGE - International Journal , 60(4), 713–717. Retrieved from https://ikm.mk/ojs/index.php/kij/article/view/6321

Most read articles by the same author(s)

1 2 > >>