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Regulatory effect of lactate on peripheral blood CD4+ T cell subsets in patients with rheumatoid arthritis
Received date: 2023-10-24
Online published: 2024-06-12
Supported by
the National Natural Science Foundation of China(82071834);the National Natural Science Foundation of China(82271839);the National Natural Science Foundation of China(82101896)
Objective: To investigate the serum lactate level in patients with rheumatoid arthritis (RA) and its relationship with disease activity, and to analyze the effect of sodium lactate on the activation of CD4+ T cells, the ability of secreting cytokines and CD4+T cell subsets in peripheral blood of the RA patients. Methods: The peripheral blood of healthy controls (HC) and RA patients was collected, and the content of lactate in the supernatant was detected by lactate detection kit, the correlation between the content of lactate and the disease score of the RA patients was analyzed; the activation level of CD4+ T cells, the proportion of CD4+ T cell subsets and the cytokines secreted by CD4+ T cells in peripheral blood of all the RA patients were detected by flow cytometry after being stimulated with sodium lactate. Results: The serum lactate level in the RA patients (n=66) was significantly higher than that in the HC (n=60, P < 0.001), and there was a certain correlation with disease activity score in 28 joints (DAS28)-C-reactive protein (CRP) (r=0.273, P=0.029), The levels of rheumatoid factor [RF, 197.50 (26.03, 783.00) IU/mL vs. 29.30 (0.00, 102.60) IU/mL, P < 0.01], CRP [37.40 (11.30, 72.60) mg/L vs. 5.83 (2.36, 12.45) mg/L, P < 0.001], were increased in patients with the lactate concentration greater than 5 mmol/L were significantly higher than those in patients with the lactate concentration less than or equal 5 mmol/L, however, there was no significant difference in the expression of erythrocyte sedimentation rate [ESR, 42.00 (19.00, 77.00) mm/h vs. 25.00 (12.50, 45.50) mm/h, P>0.05] and anti-cyclic citrullinated peptied (CCP) antibody [82.35 (17.70, 137.00) RU/mL vs. 68.60 (25.95, 119.70) RU/mL, P>0.05]. Compared with the control group, the expression of PD-1 (46.15%±8.54% vs. 41.67%±9.98%, P < 0.001), inducible costimulatory molecule (ICOS, 5.77%±8.60% vs. 18.65%±7.94%, P < 0.01) and CD25 (25.89%±5.80% vs. 22.25%±4.59%, P < 0.01) on the surface of CD4+ T cells in the RA patients treated with sodium lactate was significantly increased. Compared with the control group, the proportion of Th17 (4.62%±1.74% vs. 2.93%±1.92%, P < 0.05) and Tph (28.02%±6.28% vs. 20.32%±5.82%, P < 0.01) cells in CD4+T cells of the RA patients in the sodium lactate treatment group increased. Compared with the control group, the expression of IL-21 (5.73%±1.59% vs. 4.75%±1.71%, P < 0.05) in CD4+T cells was up-regulated in the RA patients treated with sodium lactate. Conclusion: The level of serum lactate in RA patients is increased, which promotes the activation of CD4+T cells and the secretion of IL-21, and up-regulates the proportion of Th17 and Tph cells in the RA patients.
Key words: Rheumatoid arthritis; Lactate; CD4+T cell; Peripheral helper T (Tph) cell
Huina HUANG , Jing ZHAO , Xiangge ZHAO , Ziran BAI , Xia LI , Guan WANG . Regulatory effect of lactate on peripheral blood CD4+ T cell subsets in patients with rheumatoid arthritis[J]. Journal of Peking University(Health Sciences), 2024 , 56(3) : 519 -525 . DOI: 10.19723/j.issn.1671-167X.2024.03.020
| 1 | Ding Q , Hu W , Wang R , et al. Signaling pathways in rheumatoid arthritis: Implications for targeted therapy[J]. Signal Transduct Target Ther, 2023, 8 (1): 68. |
| 2 | McInnes IB , Schett G . The pathogenesis of rheumatoid arthritis[J]. N Engl J Med, 2011, 365 (23): 2205- 2219. |
| 3 | Chen W , Yu Y , Zheng SG , et al. Human gingival tissue-derived mesenchymal stem cells inhibit proliferation and invasion of rheumatoid fibroblast-like synoviocytes via the CD39/CD73 signaling pathway[J]. Rheumatol Autoimmun, 2023, 3, 90- 99. |
| 4 | Wang D , Li Y , Liu Y , Shi G . The role of autoreactive T cell in the pathogenesis of rheumatoid arthritis and implications for T cell targeted vaccine therapy[J]. Minerva Med, 2015, 106 (3): 157- 167. |
| 5 | Yamada H . The search for the pathogenic T cells in the joint of rheumatoid arthritis: Which T-cell subset drives autoimmune inflammation[J]. Int J Mol Sci, 2023, 24 (8): 6930. |
| 6 | Chemin K , Gerstner C , Malmstr?m V . Effector functions of CD4+ T cells at the site of local autoimmune inflammation: Lessons from rheumatoid arthritis[J]. Front Immunol, 2019, 10, 353. |
| 7 | Yoshitomi H . Peripheral helper T cell responses in human diseases[J]. Front Immunol, 2022, 13, 946786. |
| 8 | Lucas C , Perdriger A , Amé P . Definition of B cell helper T cells in rheumatoid arthritis and their behavior during treatment[J]. Semin Arthritis Rheum, 2020, 50 (5): 867- 872. |
| 9 | Huang Y , Ba X , Han L , et al. T peripheral helper cells in autoimmune diseases: What do we know[J]. Front Immunol, 2023, 14, 1145573. |
| 10 | Sun S , Li H , Chen J , et al. Lactic acid: No longer an inert and end-product of glycolysis[J]. Physiology (Bethesda), 2017, 32 (6): 453- 463. |
| 11 | Ye L , Jiang Y , Zhang M . Crosstalk between glucose metabolism, lactate production and immune response modulation[J]. Cytokine Growth Factor Rev, 2022, 68, 81- 92. |
| 12 | 段姣妞, 张改连. 乳酸在类风湿关节炎发病机制及治疗中的研究进展[J]. 中华风湿病学杂志, 2022, 26 (12): 842- 845. |
| 13 | Haas R , Smith J , Rocher-Ros V , et al. Lactate regulates metabolic and pro-inflammatory circuits in control of T cell migration and effector functions[J]. PLoS Biol, 2015, 13 (7): e1002202. |
| 14 | Pucino V , Certo M , Bulusu V , et al. Lactate buildup at the site of chronic inflammation promotes disease by inducing CD4(+) T cell metabolic rewiring[J]. Cell Metab, 2019, 30 (6): 1055- 1074. e8. |
| 15 | Pucino V , Bombardieri M , Pitzalis C , et al. Lactate at the crossroads of metabolism, inflammation, and autoimmunity[J]. Eur J Immunol, 2017, 47 (1): 14- 21. |
| 16 | Chang X , Wei C . Glycolysis and rheumatoid arthritis[J]. Int J Rheum Dis, 2011, 14 (3): 217- 222. |
| 17 | Wang Q , Asenso J , Xiao N , et al. Lactic acid regulation: A potential therapeutic option in rheumatoid arthritis[J]. J Immunol Res, 2022, 2022, 2280973. |
| 18 | Rao DA , Gurish MF , Marshall JL , et al. Pathologically expanded peripheral T helper cell subset drives B cells in rheumatoid arthritis[J]. Nature, 2017, 542 (7639): 110- 114. |
| 19 | Marks KE , Rao DA . T peripheral helper cells in autoimmune diseases[J]. Immunol Rev, 2022, 307 (1): 191- 202. |
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