Evaluation of the immune feature of ACPA-negative rheumatoid arthritis and the clinical value of matrix metalloproteinase-3

• Published in: Frontiers in immunology 2022-07, Vol.13, p.939265-939265
• Main Authors: Liang, Zhaojun, Wang, Nan, Shang, Lili, Wang, Yanlin, Feng, Min, Liu, Guangying, Gao, Chong, Luo, Jing
• Format: Article
• Language: English
• Subjects: anti-citrullinated protein antibodies; biomarker; Immunology; lymphocyte subsets; matrix metalloproteinase-3; rheumatoid arthritis
• ISSN: 1664-3224; 1664-3224
• DOI: 10.3389/fimmu.2022.939265

Anti-citrullinated protein antibodies (ACPAs) are highly specific for the diagnosis of rheumatoid arthritis (RA). However, about one-third of RA patients are negative for ACPAs, which presents a challenge to the early diagnosis of RA. The purpose of this study was to analyze differences in lymphocyte subsets and CD4 + T cell subsets between ACPA + and ACPA - RA patients, and to evaluate the value of matrix metalloproteinase-3 (MMP-3) as a diagnostic and monitoring marker in ACA - RA patients. A total of 145 ACPA + RA patients, 145 ACPA - RA patients, and 38 healthy controls (HCs) were included in this study. Peripheral lymphocyte subsets were detected using flow cytometry, and serum MMP-3 was detected using chemiluminescence. Information about joint symptoms, other organ involvement, and related inflammatory markers was also collected. The results showed that, compared to ACPA - RA patients, ACPA + cases had greater imbalances between peripheral CD4 + T cell subsets, mainly manifested as an increase in T-helper 1 (Th1) cells ( p < 0.001) and decrease in regulatory T (Treg) cells ( p = 0.029). This makes these patients more prone to inflammatory reactions and joint erosion. MMP-3 levels in ACPA + and ACPA - RA patients were significantly higher than in HCs ( p < 0.001), and MMP-3 could effectively distinguish between ACPA - RA patients and HCs (area under the curve [AUC] = 0.930, sensitivity 84.14%, specificity 92.11%). MMP-3 was also a serum marker for distinguishing between RA patients with low and high disease activities. Further analysis showed that MMP-3 was positively correlated with the levels of inflammatory markers and disease activity, and negatively correlated with the levels of lymphocyte subsets. In addition, with improvements in the disease, MMP-3 levels decreased, and further increased as the patients started to deteriorate. In summary, our research showed that there was a mild imbalance between peripheral CD4 + T cell subsets in ACPA - RA patients. MMP-3 may be used as a potential marker for early diagnosis of ACPA - RA. MMP-3 was an important index for RA disease evaluation, disease activity stratification, and prognosis.