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Inhibitory Receptor Expression on T Cells as a Marker of Disease Activity and Target to Regulate Effector Cellular Responses in Rheumatoid Arthritis
Author(s) -
Onofrio Luisina I.,
Zacca Estefania R.,
Ferrero Paola,
Acosta Cristina,
Mussano Eduardo,
Onetti Laura,
Cadile Isaac,
Gazzoni M. Victoria,
Jurado Raúl,
Boari Jimena Tosello,
Ramello Maria C.,
Montes Carolina L.,
Gruppi Adriana,
Acosta Rodríguez Eva V.
Publication year - 2018
Publication title -
arthritis and rheumatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.106
H-Index - 314
eISSN - 2326-5205
pISSN - 2326-5191
DOI - 10.1002/art.40521
Subject(s) - immune system , receptor , immunology , receptor expression , t cell , cytokine , rheumatoid arthritis , effector , flow cytometry , erythrocyte sedimentation rate , medicine , cytotoxic t cell , biology , in vitro , biochemistry
Objective Inhibitory receptors are essential for the regulation of effector immune responses and may play critical roles in autoimmune diseases. We evaluated whether inhibitory receptor expression on T cells from patients with rheumatoid arthritis ( RA ) were correlated with immune activation, disease activity, and response to treatment, as well as whether inhibitory receptor–mediated pathways were functional. Methods Using flow cytometry, we performed extensive phenotypic and functional evaluation of CD 4+ and CD 8+ T cells from the blood and synovial fluid ( SF ) of RA patients ex vivo and after culture. The relationship of each parameter with the Disease Activity Score in 28 joints using the erythrocyte sedimentation rate ( DAS 28‐ ESR ) and response to treatment was examined. Results In RA patients with low levels of T cell activation, inhibitory receptor expression showed an inverse relationship with the DAS 28‐ ESR . The frequency of T cells expressing multiple inhibitory receptors was reduced in untreated RA patients but returned to normal levels in treated patients. RA patients who responded to treatment showed an augmented frequency of inhibitory receptor–expressing T cells that correlated with reduced inflammatory cytokine production in comparison to nonresponders. Higher frequencies of effector and memory T cells that expressed multiple inhibitory receptors were seen in SF than in peripheral blood. Notably, inhibitory pathways were operative in blood and synovial T cells from all RA patients, although cells from nonresponder patients were less sensitive to inhibition. Conclusion Inhibitory receptor expression on T cells from RA patients is inversely correlated with effector T cell function and disease activity and may predict response to treatment. Furthermore, different inhibitory pathways are functional and cooperatively suppress synovial T cells, providing a rationale for new treatment strategies to regulate acute local inflammation.