Objective This study examines polyfunctional T-cells in psoriatic arthritis (PsA) synovial tissue and their associations with clinical disease and implications for therapy.
Methods PsA synovial tissue was enzymatically/mechanically digested to generate synovial tissue single cell suspensions. Frequencies of polyfunctional CD4, CD8, T-helper 1 (Th1), Th17 and exTh17 cells, using CD161 as a marker of Th17 plasticity, were determined by flow cytometry in matched PsA synovial tissue and peripheral blood. Synovial T-cell polyfunctionality was assessed in relation to Disease Activity in PSoriatic Arthritis (DAPSA) and in synovial cell suspensions cultured with a current mode of treatment, phosphodiesterase 4 (PDE4) inhibitor.
Results PsA synovial tissue infiltrating CD4+ T-cells expressed higher levels of interleukin (IL)-17A, interferon gamma (IFN-γ), GM-CSF and CD161, with parallel enrichment of Th1, Th17 and exTh17 T-helper subsets (all p<0.05). Interestingly, a significant proportion of synovial T-cell subsets were triple-positive for GM-CSF, tumour necrosis factor (-TNF), -IL-17 or IFN-γ compared with matched blood (all p<0.05). Importantly, frequencies of polyfunctional T-cells correlated with DAPSA: Th1-GM-CSF+/TNF+/IFN-γ+ (r=0.7, p<0.01), Th17-GM-CSF+/TNF+/IL-17+ (r=0.6, p<0.057) and exTh17-GM-CSF+/TNF+/IFN-γ+ (r=0.7, p=0.0096), with no associations observed for single cytokine-producing T-cells. Following ex vivo culture of PsA synovial tissue cell suspensions, polyfunctional GM-CSF+TNFα+IL-17A+ or/IFN-γ+-producing T-cells (p<0.05), but not single cytokine-producing T-cells, were inhibited with a PDE4 inhibitor.
Conclusion These data demonstrate enrichment of polyfunctional T-cells in PsA synovial tissue which were strongly associated with DAPSA and ex vivo therapeutic response.
- psoriatic arthritis
- synovial tissue
- polyfunctional t-cells
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What is already known about this subject?
T-cells and their cytokines play a critical role in psoriatic arthritis (PsA) pathophysiology.
Previous T-cell studies in PsA have focused on circulating and/or synovial fluid cells.
What does this study add?
This is the first report of enrichment of a specific subset of novel polyfunctional T-cells in the synovial tissue from patients with PsA.
How might this impact on clinical practice or future developments?
PsA synovial tissue polyfunctional T-cells significantly correlate with disease activity (Disease Activity in PSoriatic Arthritis) and response, thereby may guide treatment decisions and prognosis.
Psoriatic arthritis (PsA) is a chronic inflammatory arthropathy associated with psoriasis. Synovial inflammation is a pathological hallmark of PsA, characterised by dysfunctional angiogenesis, activation of synovial fibroblasts and infiltration of immune cells.1 2 Genetic and functional studies strongly support the role of T-cells in PsA pathogenesis. As a result, the targeted inhibition of dysfunctional T-cells in PsA has been an area of intensive investigation. Both CD4 and CD8 T-cells are found in abundance in the PsA synovium,2 3 with increased expression of the chemokine receptor C-C chemokine receptor type 4 (CCR4), a key component of T-cell migration, also observed in synovial tissue and fluid.3 CD8 T-cells are clonally expanded in PsA synovium,4 5 while synovial enriched interleukin (IL)-17+CD8+ T-cells correlate with erosive disease.6 Within the CD4 T-cell compartment, several studies demonstrate elevated frequencies of circulatory T-helper 17 (Th17) cells in patients with PsA, with even higher numbers in the synovial fluid.6 Accumulating evidence suggests Th17 cells in PsA synovial fluid are associated with polyfunctional cytokine expression,7 where multiple cytokines including tumour necrosis factor alpha (TNFα), granulocyte-macrophage colony-stimulating factor (GM-CSF and IL-22 are produced simultaneously and augment the complex local inflammatory environment.8 Indeed, T-cells have been recently targeted by modulation of T-cell costimulation,9 anti-IL-17 antibodies10 and blockade of the IL-23/IL-12 axis,11 but with somewhat variable results. The effective targeting of T-cells requires a detailed characterisation of synovial T-cells and a full understanding of how these cells behave at the site of inflammation. However, as the T-cell profile of PsA synovial tissue has only been examined by immunohistochemistry or T-cell repertoire studies, little is known about the frequency of Th cell subsets, T-cell polyfunctionality and their relation to disease activity and therapy response.
In this study, for the first time, we demonstrate enrichment of synovial tissue polyfunctional CD4, CD8, Th1, Th17 and exTh17 cells compared with their circulatory counterparts. Furthermore, we show that it is these synovial tissue infiltrating polyfunctional T-cells, and not single cytokine-producing T-cells, that positively correlate with the clinical disease activity measure, Disease Activity in PSoriatic Arthritis (DAPSA), and response to therapy in ex vivo synovial cell cultures, suggesting these T-cell subsets play a key role in PsA pathogenesis.
Materials and methods
Enrichment of polyfunctional T-cells in PsA synovial tissue
The frequency of synovial CD8+, CD4+, Th1, Th17 and exTh17 cells and their ability to produce a combination of key T-cell-associated cytokines—interferon gamma (IFN-γ), GM-CSF, TNFα and IL-17A—was evaluated using multiparameter flow cytometry (gating strategy in online supplementary figure 1) on matched peripheral blood and synovial tissue from patients with PsA (online supplementary table 1). The frequency of CD4-derived IFN-γ+, IL-17A+ and GM-CSF+ was significantly increased in the synovial tissue of patients with PsA as compared with matched peripheral blood (all p<0.05; figure 1A). In contrast, the frequency of CD4 TNF+ T-cells was significantly decreased in PsA synovial tissue (p<0.05). Within the CD4 compartment, the levels of Th17 lineage marker, CD161, were significantly increased in PsA synovial tissue (p<0.05) (figure 1B). Using CD161 expression and cytokine expression, we demonstrated a significant increase in the frequency of Th1-CD161−IFN-γ+(p<0.05), Th17-CD161+IL-17A+ (p<0.05) and exTh17-CD161+IFN-γ+ (p<0.05) in PsA synovial tissue compared with peripheral blood (figure 1B). No significant difference in the frequency of GM-CSF+, TNFα+, IL-17A+ and IFN-γ+ CD8 T-cells was observed in PsA synovial tissue (online supplementary figure 2).
Using Boolean gating strategy and SPICE software, we next explored the monofunctional and polyfunctional cytokine combinations produced by synovial resident and circulating T-cells in PsA, which demonstrated striking differences in synovial T-cells cytokine production compared with circulating T-cells (figure 1C). Single cytokine-positive cells are represented by individual arcs surrounding the pie charts, while double, triple and quadruple cytokine-positive T-cells were represented by overlapping arcs (figure 1C). A significant proportion of synovial T-cell subsets (CD4, CD8, Th1, Th17 and exTh17 cells) were triple-positive for GM-CSF+TNF+IL-17+or IFN-γ+ compared with matched peripheral blood T-cells (all p<0.05). In particular, increased frequency of triple-positive synovial T-cells simultaneously secreting GM-CSF, TNFα and IL-17A (pie chart, orange segment) or GM-CSF, TNFα and IFN-γ (pie chart, green segment) as compared with the peripheral blood was observed. The frequency of triple cytokine-positive T-cells was also increased in PsA synovial tissue compared with osteoarthritis (OA) synovium (online supplementary figure 3). Overall, a significant shift towards higher cytokine polyfunctionality in synovial tissue T-cells versus peripheral blood with paralleled decreases in frequency of single cytokine-producing T-cells was demonstrated (p<0.05; figure 1C).
Positive correlation between polyfunctional synovial tissue Th1, Th17 and exTh17 cells with disease activity
The relationship between T-cell polyfunctionality and synovial inflammation was then examined in relation to disease activity by comparing the frequency of triple and single cytokine-positive synovial T-cells with DAPSA.12 Significant positive correlations were demonstrated between DAPSA and frequency of triple-positive infiltrating synovial T-cells GM-CSF+TNFα+IFN-γ+ (r=0.70,p<0.01), Th17-GM-CSF+/TNF+/IL-17+ (r=0.6, p<0.057) and exTh17-GM-CSF+/TNF+/IFN-γ+ (r=0.7, p=0.0096; figure 2A). In contrast, single cytokine-producing synovial tissue Th1, Th17 and exTh17 cells did not positively correlate with any clinical measures of disease; indeed negative associations were observed (figure 2B). These data suggest that rather than their absolute frequencies, it is the polyfunctional cytokine capacity of synovial T-cells which is important in PsA disease pathogenesis.
Effect of PDE4 blockade on polyfunctional synovial T-cells
To examine if current therapies routinely used in the clinic affect synovial infiltrating T-cells’ polyfunctionality, we next investigated in ex vivo PsA synovial tissue cell suspensions the effect of phosphodiesterase 4 (PDE4) inhibition on CD4, CD8, Th1, Th17 and exTh17 cytokine production. A significant reduction in cytokine polyfunctionality in rolipram-treated synovial suspensions was demonstrated (p<0.05, figure 3A; dose-dependent response in online supplementary figure 4). In particular, a significant reduction in the proportion of GM-CSF, TNFα, IL-17A and/or IFN-γ triple-positive (orange/green segments) synovial CD4, CD8 (p<0.05), Th1 (p<0.05), Th17 (p<0.05) and exTh17 (p<0.05) (figure 3B, upper right quadrants, and figure 3C). Furthermore, these effects were not observed for single cytokine-producing T-cells, where the frequency of IFN-γ only, Th1 and exTh17 cells (dark blue segment) was significantly increased in response to rolipram treatment (both p<0.05; and online supplementary figure 5), with similar effects observed for IL-17A-only cells (dark purple segment and online supplementary figure 2).
This is the first study to examine T-cell polyfunctionality in single cell suspensions isolated from PsA synovial tissue and their association with measures of clinical disease activity. Flow cytometric analysis of synovial T-cells characterised a distinct T-cell signature that comprised enriched Th1, Th17 and exTh17 cells in PsA synovial tissue as compared with circulating T-cells, which were more polyfunctional in nature. Polyfunctional synovial tissue T-cells significantly correlated with PsA disease activity measures, in contrast to monofunctional T-cells, which negatively correlated with disease activity. Following ex vivo culture of PsA synovial tissue cell suspensions, polyfunctional GM-CSF+TNFα+IL-17A+ and/or IFN-γ+-producing T-cells, and not single cytokine-producing T-cells, were effectively inhibited by a PDE4 inhibitor, further suggesting that synovial tissue polyfunctional T-cells contribute to PsA pathogenesis.
In this study, we report for the first time elevated frequencies of Th1, Th17 and exTh17 cells in the synovium of patients with PsA. The Th17 lineage marker, CD161, was significantly elevated in PsA synovial tissue, suggesting a strong Th17 phenotype in PsA synovial pathology, which is consistent with previous findings.12–15 However, our data indicated that exTh17 and Th17 cells that have transitioned are also highly enriched in the PsA joint. While several studies have demonstrated Th17 plasticity in chronic inflammation, with elevated frequencies of exTh17 cells reported in psoriasis16 and rheumatoid arthritis synovial fluid,17 the mechanism for this remains unknown; however, IL-12 and IL-23, both implicated in PsA, have demonstrated the ability to promote Th17 plasticity in vitro.18 Despite being called non-classical Th1 cells, the joint specific Th17 lineage, exTh17 cells exhibit distinct pathogenic characteristics, including greater cytokine production, increased proliferation and resistance to Treg suppression.17 Our data now indicate that exTh17 cells are also likely to contribute to disease pathogenesis in PsA.
We also provide evidence that polyfunctional cytokine-expressing synovial T-cells may be key pathogenic mediators of PsA synovial inflammation. Synovial infiltrating T-cells exhibited greater cytokine polyfunctionality, particularly GM-CSF+TNF+IFN-γ+ or IL-17A+ positive T-cells, as compared with matched blood. Importantly, polyfunctional synovial T-cells, and not monofunctional single cytokine-producing T-cells, were positively associated with DAPSA, suggesting they are highly pathogenic in nature. This is consistent with previous studies showing augmented Th17 differentiation and polyfunctional cytokine expression with parallel skin hyperkeratosis, enthesitis and bone erosion in cutaneous and synovio-entheseal inflammation model of PsA.19 Interestingly, it has also been shown that antigen-specific T-cells exhibit cytokine polyfunctionality and enhanced immunity.20 This may be of particular interest for PsA as human leukocyte antigen (HLA)-27 polymorphism and infection are a recognised feature of PsA pathophysiology.
A PDE4 inhibitor reduced triple cytokine-positive GM-CSF+TNF+IFN-γ+ and IL-17A+ T-cells. Previous studies have demonstrated the targeted inhibition of T-cell-derived TNFα, IFN-γ, IL-2, IL-4 and IL-17A in PsA peripheral blood in response to apremilast treatment21; however, the findings in this study now provide preliminary insights into potentially novel anti-inflammatory mechanisms in PsA synovial tissue. While the exact mechanism by which PDE4 blockade suppresses these polyfunctional T-cells is unclear, previous studies have demonstrated the importance of janus kinase/signal transducer and activator of transcription (JAK/STAT) signalling in synovial T-cell differentiation,22 while the deletion of STAT5 in CD4 T-cells significantly impaired GM-CSF expression by CD4 T-cell.23
In conclusion, this is the first study to perform a detailed phenotypic analysis of synovial infiltrating T-cells in PsA. Synovial T-cells are polyfunctional in terms of cytokine expression, are positively associated with disease activity and are effectively repressed by PDE4 blockade. These data suggest that polyfunctional T-cells contribute to PsA pathogenesis.
Handling editor Professor Josef S Smolen
Contributors SMW, MC, DJV, UF: developed the concept and wrote the paper. SMW, MC, TMG, SCW, CL, RHM, DJV, UF: generated and interpreted the data. UF, DJV: supervised the project. All authors critically reviewed and edited the paper.
Funding This study was sponsored by IRCSET and Arthritis Ireland.
Competing interests None declared.
Patient consent for publication Obtained.
Ethics approval Ethical approval to conduct this study was granted by St Vincent’s Healthcare Group Medical Research and Ethics Committee and the Tallaght Hospital/St James's Hospital Joint Research Ethics Committee. All experiments were performed in accordance with these guidelines and regulations.
Provenance and peer review Not commissioned; externally peer reviewed.
Data sharing statement All data from this study were published in the article or in the online supplementary information.
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