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The expression of interferon-stimulated genes (interferon “signature”) in patients with rheumatoid arthritis (Preliminary results)

https://doi.org/10.47360/1995-4484-2020-673-677

Abstract

Objective. To assess the expression of interferon-stimulated genes in patients with rheumatoid arthritis (RA).

Material and methods. Twenty patients with RA were examined. All patients received methotrexate therapy at a stable dose (Me 15 [10-17.5] mg) for at least 4 weeks. To assess the Type I IFN gene signature (IFNGS) we selected five genes (IFI44L, MX1, IFIT1, RSAD2, EPSTI1). The expression of IFI44L and IFIT1 could not be determined, and further analysis took into account three genes - MX1, EPSTI1, RSAD2.

Results. Baseline level of MX1 expression - 11.48 [5.45-19.38], EPSTI1 - 12.83 [5.62-19.64], RSAD2 - 5.16 [2.7310.4] and IFN score - 10.3 [5.18-17.12] in patients with rheumatoid arthritis was significantly higher compared with healthy donors - 1.26 [0.73-1.6], 1.06 [0.81-1.48], 0.93 [0.72-1.19], and 1.09 [0.92-1.42] respectively, p<0.05. IFN signature was found in 15 (75%) patients, was absent - in 5 (15%) patients. A positive correlation was found between the IFNGS and the level of EPSTI1 expression with the duration of methotrexate therapy (r=0.46, p=0.03). Among patients who received methotrexate therapy for more than one year, there was a tendency to a higher level of EPSTI1 expression (10.74 [12.6-32.8]) and IFNGS (16.2 [8.9-38.3]) compared with patients taking methotrexate for less than a year (9.67 [5.4-14.2] and 7.9 [4.5-13.4]), (p=0.06).

Conclusion. Preliminary results on the assessment of IFNGS indicate an increased expression of IFN-stimulated genes in patients with RA, which may be important for predicting the course of the disease and personalizing therapy.

About the Authors

A. S. Avdeeva
V.A. Nasonova Research Institute of Rheumatology
Russian Federation

Anastasiya S. Avdeeva

115522, Moscow, Kashirskoye Highway, 34A


Competing Interests: not


E. V. Tchetina
V.A. Nasonova Research Institute of Rheumatology
Russian Federation

Elena V. Tchetina

115522, Moscow, Kashirskoye Highway, 34A


Competing Interests: not


M. V. Cherkasova
V.A. Nasonova Research Institute of Rheumatology
Russian Federation

Mariya V. Cherkasova

115522, Moscow, Kashirskoye Highway, 34A


Competing Interests: not


G. A. Markova
V.A. Nasonova Research Institute of Rheumatology
Russian Federation

Galina A. Markova

115522, Moscow, Kashirskoye Highway, 34A


Competing Interests: not


A. S. Artyuhov
Research Institute of Translational Medicine, N.I. Pirogov Russian National Research Medical University
Russian Federation

Alexander S. Artyuhov

117997, Moscow, Ostrovitianova str., 1


Competing Interests: not


E. B. Dashinimaev
Research Institute of Translational Medicine, N.I. Pirogov Russian National Research Medical University; Koltzov Institute of Developmental Biology of Russian Academy of Sciences
Russian Federation

Erdem B. Dashinimaev

117997, Moscow, Ostrovitianova str., 1; 119334, Moscow, Vavilova str., 26


Competing Interests: not


E. L. Nasonov
V.A. Nasonova Research Institute of Rheumatology; I.M. Sechenov First Moscow State Medical University (Sechenovskiy University)
Russian Federation

Evgeny L. Nasonov

115522, Moscow, Kashirskoye Highway, 34A; 119991, Moscow, Trubetskaya str., 8, building 2


Competing Interests: not


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For citations:


Avdeeva A.S., Tchetina E.V., Cherkasova M.V., Markova G.A., Artyuhov A.S., Dashinimaev E.B., Nasonov E.L. The expression of interferon-stimulated genes (interferon “signature”) in patients with rheumatoid arthritis (Preliminary results). Rheumatology Science and Practice. 2020;58(6):673-677. (In Russ.) https://doi.org/10.47360/1995-4484-2020-673-677

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ISSN 1995-4484 (Print)
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