Abstract

Sarcoidosis is a disorder of unknown etiology characterized by development of necrosis-free epithelioid cell granulomas in various tissues. There are two main phenotypes of pulmonary sarcoidosis (PS): Lofgren’s syndrome (LS) is an acute form with favorable outcome, while non-Lofgren’s syndrome (nLS) is a chronic type of disease that can lead to pulmonary fibrosis in 20% of cases.Our study was aimed at investigating changes in the main cell-surface differentiation antigens on peripheral blood regulatory T cells (Tregs) from the patients with first diagnosed PS without treatment (LS, n = 11) and nLS (n = 46) compared to healthy volunteers (HC, n = 26).These indexes might be used as immunological markers for predicting severity of this disorder. Flow cytometry analysis of peripheral blood cell samples demonstrated that the nLS patients had decreased relative numbers of CD3+ cells vs healthy controls, as well as diminished CD3+CD4+ cells vs HC and LS patients. Furthermore, the relative and absolute Treg numbers were also decreased in nLS group vs HC (2.83% (2.47; 3.36) vs 3.33% (2.79; 3.84), p = 0.021), and 37 (29; 52) cells vs 50 (42; 65), p = 0.004, respectively) per one microliter of peripheral blood. Relative number of CD39-positive Тregs in chronic vs acute sarcoidosis patients was associated with 51.02% (38.20; 61.62) vs 48.64% (41.46; 63.72) that was significantly (p < 0.001 and p = 0.007, respectively) higher than in HC (39.52% (11.55; 46.34). We have found that “naïve” (CD45R0-CD62L+) Тregs did not significantly differ in percentage of CD39- and CD73-positive cells in all the groups tested. Moreover, CD45R0+CD62L+ Тregs in LS and nLS patients contained significantly more CD39-positive cells (69.66% (61.92; 79.34) and 67.62% (61.92; 79.34), respectively, compared to 47.55% (15.74; 65.32) in HC (p < 0.001 and p = 0.004, respectively). In case of CD45R0 + CD62LTregs able to exit from the circulation and migrate to the site of inflammation, an increased percentage of CD39-positive subset was noted only in patients with chronic sarcoidosis and HC (61.79% (55.12; 73.09) and 57.27% (16.03; 66.98), p = 0.006). Enhanced CD39 expression on Tregs seems to be related to chronic immune response, so that antigen elimination becomes impossible due to Treg overactivation, as shown in patients with sarcoidosis and some other chronic autoimmune and infectious disorders.

Highlights

  • Sarcoidosis is a disorder of unknown etiology characterized by development of necrosis-free epithelioid cell granulomas in various tissues [14; 32]

  • Flow cytometry analysis of peripheral blood samples demonstrated that patients with primary chronic sarcoidosis vs control group had decreased both relative (70.83% (63.93; 77.26) vs (77.06% (75.33; 78.52), respectively, p < 0.001) and absolute numbers (931 (717; 1086) vs 1218 (964; 1758) cells per 1 μL of peripheral blood, respectively, p = 0.010) of total CD3+T cells

  • It was shown that the number of peripheral blood total T cells, helper T cells as well as Tregs was significantly decreased in patients with primary chronic sarcoidosis compared to control group, which is in agreement with the concept of compartmentalized immune responses and redistribution of effector immune cells exiting peripheral circulation and entering site of inflammation [16, 34]

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Summary

Introduction

Sarcoidosis is a disorder of unknown etiology characterized by development of necrosis-free epithelioid cell granulomas in various tissues [14; 32]. A major role in pathogenesis of sarcoidosis is played solely by these cells able to. Регуляторные Т-клетки при саркоидозе Regulatory T cells in sarcoidosis activate simultaneously tissue macrophages as well as polymorphonuclear leukocytes migrating from peripheral blood to the site of inflammation [34]. Still it remains unclear what T cell subset migrating to target organs as well as genetic predisposition factors are responsible for beneficial or unfavorable course of sarcoidosis. Various forms of sarcoidosis may develop due to distinct immunoregulatory mechanisms either contributing to regression or resulting in chronic course and fibrogenesis

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