• Joanna Bartosińska, Ewelina Zakrzewska, Anna Król, Dorota Raczkiewicz, Joanna Purkot, Maria Majdan, Dorota Krasowska, Grażyna Chodorowska, and Krzysztof Giannopoulos.
• Pol. Arch. Med. Wewn. 2017 Dec 22; 127 (12): 815-822.

AbstractINTRODUCTION    Rheumatoid arthritis (RA) and psoriatic arthritis (PsA) are characterized by chronic inflammatory processes mediated by proinflammatory cytokines that affect the synovial lining. Programmed death 1 (PD‑1) is a critical regulator of T‑cell activation by downregulating immune responses.  OBJECTIVES    The aim of the study was to investigate whether the expression of PD‑1 on CD4+ and CD8+ T cells differs between patients with RA and those with PsA. PATIENTS AND METHODS    The study included 100 patients with RA, 31 patients with PsA, and 52 healthy controls. The percentages, absolute numbers, and mean fluorescence intensity (MFI) of CD4+PD‑1+ and CD8+PD‑1+T cells from peripheral blood were analyzed using flow cytometry. RESULTS    The percentages and absolute numbers of CD4+ and CD8+ T cells with PD‑1 expression were significantly higher in patients with RA than in controls. In patients with PsA, the percentages of CD4+PD‑1+ and CD8+PD‑1+ T cells were significantly lower than in controls. Because of the high frequency of PD-1‑positive T cells in RA and their low frequency in PsA, we analyzed the expression level by analyzing the MFI. The median MFI of PD‑1 on CD4+ and CD8+ T cells was significantly higher in patients with RA (median, 421 and 437, respectively) in comparison with patients with PsA (median, 222 and 198, respectively) and controls (median, 205 and 187, respectively). CONCLUSIONS    The differential expression of PD‑1 in RA and PsA suggests that PD‑1 might be involved in autoimmune mechanisms in RA and autoinflammatory mechanisms in PsA in a different manner.

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