IL-17A, IL-17F and IL-23 in patients with rheumatoid arthritis
https://doi.org/10.47360/1995-4484-2024-402-407
Abstract
The aim of the study was to determine the clinical and diagnostic value of interleukin (IL) 17A, IL-17F and IL-23 in rheumatoid arthritis (RA) patients in the advanced stage of the disease.
Materials and methods. We examined 154 patients with a reliable diagnosis of RA according to ACR/EULAR (American College of Rheumatology/European Alliance of Associations for Rheumatology) criteria (2010), predominantly (73.4%) female, middle-aged (56.0 (50.0; 64.0) years), disease duration of 9.4 (3.0; 13.0) years, radiologic stages II (34.4%) and III (37.0%), and moderate to high activity (DAS28-ESR – 5.40 (4.65; 6.00). 83.8% of patients were seropositive for IgM rheumatoid factor (IgM RF) and 68.8% had antibodies to cyclic citrullinated peptide (ACCP). 144 (93.5%) patients were taking DMARDs (methotrexate, leflunamide, sulfasalazine) as well as nonsteroidal antiinflammatory drugs (NSAIDs) and glucocorticoids (GCs) up to 10 mg/day in terms of prednisolone.
The serum levels of IL-17A, IL-17F and IL-23 were investigated using multiplex xMAR technology. The upper limit of norm (M+3σ) in 20 sera of healthy donors was 1.78 pg/mL for IL-17A, 9.5 pg/mL for IL-17F and 91.55 pg/mL for IL-23.
Results. IL-17A (1.16 (0.50; 2.39) pg/mL) and IL-17F (5.02 (1.00; 138.80) pg/mL) concentrations in RA patients were not significantly different from controls (0.78 (0.00; 1.65) and 4.02 (1.46; 7.31) pg/mL; p>0.05). In contrast, IL-23 levels were significantly higher in patients than in donors (21.36 (2.50; 4626.22) and 14.63 (0.00; 91.55) pg/mL; p<0.05). High values of IL-17F (71 patients – 46.1%) and IL-23 (66 patients – 42.9%) were significantly more frequently detected than IL-17A (46 patients – 29.9%; p=0.003 and p=0.02, respectively). Hyperproduction of IL-17A and IL-17F was simultaneously observed in 37 (24.0%) patients, and 32 (20.8%) patients had an increase in IL-17A, IL-17F and IL-23. Correlations between IL-17A and IL-17F concentration (r=0.44; p<0.05), IL-17A and IL-23 (r=0.40; p<0.05), IL-17F and IL-23 (r=0.94; p<0.05) were found. No statistically significant differences were observed between the concentration of IL-17A, IL-17F, IL-23 and the frequency of their elevation in RA patients positive or negative for IgM RF, as well as ACCP. When IL-17A level was elevated, CDAI (Clinical Disease Activity Index) and SDAI (Simplified Disease Activity Index) indices and IgM RF concentration were significantly higher than in the comparison group (p<0.05). In patients with IL-17F hyperproduction predominance of ESR and C-reactive protein values was revealed in comparison with normal values of this index (p<0,05). At the same time, IL-17A concentration correlated with SDAI (r=0,17; p<0,05), IgM RF values (r=0,19; p<0,05) and ACCP (r=0,19; p<0,05). When IL-23 values were high, the HR was significantly lower 28 (p<0.05), and the groups did not differ in other measures of disease activity, IgM RF and ACCP. No differences in clinical and laboratory indicators of RA activity were found between patients with simultaneous elevation of one, two or three cytokines and groups of patients with their normal concentrations. In RA patients in the advanced stage of the disease, IL-17F hyperproduction prevails over the frequency of IL-17A elevation. The concentration of IL-23 in serum is significantly higher in patients with RA compared to the control group, and its high values are found in 42.7% of patients. The combined hyperproduction of IL-17A and IL-17F; IL-17A, IL-17F and IL-23 does not increase the proinflammatory potential of each individual cytokine. |
About the Authors
Natalia A. LapkinaRussian Federation
150000, Yaroslavl, Revolyutsionnaya str., 5
Andrey A. Baranov
Russian Federation
150000, Yaroslavl, Revolyutsionnaya str., 5
Olga P. Rechkina
Russian Federation
150000, Yaroslavl, Revolyutsionnaya str., 5
Natalia E. Abaytova
Russian Federation
150000, Yaroslavl, Revolyutsionnaya str., 5
Svetlana S. Zolotavkina
Russian Federation
150000, Yaroslavl, Revolyutsionnaya str., 5
Alexander S. Artyuhov
Russian Federation
117997, Moscow, Ostrovitianova str., 1
Evgeny L. Nasonov
Russian Federation
115522, Moscow, Kashirskoye Highway, 34A
119991, Moscow, Trubetskaya str., 8, building 2
References
1. McGeachy MJ, Cua DJ, Gaffen SL. The IL-17 family of cytokines in health and disease. Immunity. 2019;50(4):892-906. doi: 10.1016/j.immuni.2019.03.021
2. Nasonov EL. New possibilities of pharmacotherapy for immunoinflammatory rheumatic diseases: A focus on inhibitors of interleukin-17. Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2017;55(1):68-86 (In Russ.)]. doi: 10.14412/1995-4484-2017-68-86
3. Nasonov EL, Korotaeva TV, Dubinina TV, Lila AM. IL-23/IL-17 inhibitors in immunoinflammatory rheumatic diseases: New horizons. Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2019;57(4):400-406 (In Russ.)]. doi: 10.14412/1995-4484-2019-400-406
4. Nasonov EL, Avdeeva AS, Korotaeva TV, Dubinina TV, Usacheva JV. The role of interleukin 17 in the pathogenesis of rheumatoid arthritis. Are there any prospects for the use of IL-17 inhibitors? Nauchno-Prakticheskaya Revmatologia = Rheumatology Science and Practice. 2023;61(2):165-180 (In Russ.)]. doi: 10.47360/1995-4484-2023-165-180
5. Beringer A, Miossec P. Systemic effects of IL-17 in inflammatory arthritis. Nat Rev Rheumatol. 2019;15(8):491-501. doi: 10.1038/s41584-019-0243-5
6. Lubberts E. The IL-23-IL-17 axis in inflammatory arthritis. Nat Rev Rheumatol. 2015;11(7):415-429. doi: 10.1038/nrrheum.2015.53
7. Novikov AA, Aleksandrova EN, Lukina GV. Serum cytokine profile in early and established rheumatoid arthritis. Almanac of Clinical Medicine. 2019;47(5):393-399 (In Russ.)]. doi: 10.18786/2072-0505-2019-47-058
8. Guo YY, Wang NZ, Zhao S, Hou LX, Xu YB, Zhang N. Increased interleukin-23 is associated with increased disease activity in patients with rheumatoid arthritis. Chin Med J (Engl). 2013;126(5):850-854.
9. Al-Saadany HM, Hussein MS, Gaber RA, Zaytoun HA. Th-17 cells and serum IL-17 in rheumatoid arthritis patients: Correlation with disease activity and severity. The Egyptian Rheumatologist. 2016;38(1):1-7. doi: 10.1016/j.ejr.2015.01.001
10. Abu Al Fadl EM, Fattouh M, Allam AA. High IL-23 level is a marker of disease activity in rheumatoid arthritis. Egypt J Immunol. 2013;20(2):85-92.
11. Aletaha D, Neogi T, Silman AJ, Funovits J, Felson DT, Bingham CO 3rd, et al. 2010 rheumatoid arthritis classification criteria: An American College of Rheumatology/European League Against Rheumatism collaborative initiative. Arthritis Rheum. 2010;62(9): 2569-2581. doi: 10.1002/art.27584
12. Taams LS. Interleukin-17 in rheumatoid arthritis: Trials and tribulations. J Exp Med. 2020;217(3):e20192048. doi: 10.1084/jem.20192048
13. Miossec P. Local and systemic effects of IL-17 in joint inflammation: A historical perspective from discovery to targeting. Cell Mol Immunol. 2021;18(4):860-865. doi: 10.1038/s41423-021-00644-5
14. Liu C, Chu D, Kalantar-Zadeh K, George J, Young HA, Liu G. Cytokines: From clinical significance to quantification. Adv Sci (Weinh). 2021;8(15):e2004433. doi: 10.1002/advs.202004433
15. Metawi SA, Abbas D, Kamal MM, Ibrahim MK. Serum and synovial fluid levels of interleukin-17 in correlation with disease activity in patients with RA. Clin Rheumatol. 2011;30(9):1201-1207. doi: 10.1007/s10067-011-1737-y
16. Siloşi I, Boldeanu MV, Cojocaru M, Biciuşcă V, Pădureanu V, Bogdan M, et al. The relationship of cytokines IL-13 and IL-17 with autoantibodies profile in early rheumatoid arthritis. J Immunol Res. 2016;2016:3109135. doi: 10.1155/2016/3109135
17. Costa CM, Santos MATD, Pernambuco AP. Elevated levels of inflammatory markers in women with rheumatoid arthritis. J Immunoassay Immunochem. 2019;40(5):540-554. doi: 10.1080/15321819.2019.1649695
18. Schofield C, Fischer SK, Townsend MJ, Mosesova S, Peng K, Setiadi AF, et al. Characterization of IL-17AA and IL-17FF in rheumatoid arthritis and multiple sclerosis. Bioanalysis. 2016;8(22):2317-2327. doi: 10.4155/bio-2016-0207
19. Misra S, Mondal S, Chatterjee S, Dutta S, Sinha D, Bhattacharjee D, et al. Interleukin-17 as a predictor of subclinical synovitis in the remission state of rheumatoid arthritis. Cytokine. 2022;153:155837. doi: 10.1016/j.cyto.2022.155837
20. Ndongo-Thiam N, Miossec P. A cell-based bioassay for circulating bioactive IL-17: Application to destruction in rheumatoid arthritis. Ann Rheum Dis. 2015;74(8):1629-1631. doi: 10.1136/annrheumdis-2014-207110
21. Gullick NJ, Abozaid HS, Jayaraj DM, Evans HG, Scott DL, Choy EH, et al. Enhanced and persistent levels of interleukin (IL)17+ CD4+ T cells and serum IL-17 in patients with early inflammatory arthritis. Clin Exp Immunol. 2013;174(2):292-301. doi: 10.1111/cei.12167
22. Lee K, Min HK, Koh SH, Lee SH, Kim HR, Ju JH, et al. Prognostic signature of interferon-γ and interleurkin-17A in early rheumatoid arthritis. Clin Exp Rheumatol. 2022;40(5):999-1005. doi: 10.55563/clinexprheumatol/mkbvch
23. Raza K, Falciani F, Curnow SJ, Ross EJ, Lee CY, Akbar AN, et al. Early rheumatoid arthritis is characterized by a distinct and transient synovial fluid cytokine profile of T cell and stromal cell origin. Arthritis Res Ther. 2005;7:R784-95. doi: 10.1186/ar1733
24. Kokkonen H, Söderström I, Rocklöv J, Hallmans G, Lejon K, Rantapää Dahlqvist S. Up-regulation of cytokines and chemokines predates the onset of rheumatoid arthritis. Arthritis Rheum. 2010;62:383-391. doi: 10.1002/art.27186
25. Yang XO, Chang SH, Park H, Nurieva R, Shah B, Acero L, et al. Regulation of inflammatory responses by IL-17F. J Exp Med. 2008;205(5):1063-1075. doi: 10.1084/jem.20071978
26. Burns LA, Maroof A, Marshall D, Steel KJA, Lalnunhlimi S, Cole S, et al. Presence, function, and regulation of IL-17F-expressing human CD4+ T cells. Eur J Immunol. 2020;50(4):568-580. doi: 10.1002/eji.201948138
27. Zaky DS, El-Nahrery EM. Role of interleukin-23 as a biomarker in rheumatoid arthritis patients and its correlation with disease activity. Int Immunopharmacol. 2016;31:105-108. doi: 10.1016/j.intimp.2015.12.011
28. Kim HR, Cho ML, Kim KW, Juhn JY, Hwang SY, Yoon CH, et al. Up-regulation of IL-23p19 expression in rheumatoid arthritis synovial fibroblasts by IL-17 through PI3-kinase-, NF-kappaB- and p38 MAPK-dependent signalling pathways. Rheumatology (Oxford). 2007;46(1):57-64. doi: 10.1093/rheumatology/kel159
Review
For citations:
Lapkina N.A., Baranov A.A., Rechkina O.P., Abaytova N.E., Zolotavkina S.S., Artyuhov A.S., Nasonov E.L. IL-17A, IL-17F and IL-23 in patients with rheumatoid arthritis. Rheumatology Science and Practice. 2024;62(4):402–407. (In Russ.) https://doi.org/10.47360/1995-4484-2024-402-407