Expression and Function of the Costimulatory Receptor SLAMF1 Is Altered in Lymphocytes From Patients With Autoimmune Thyroiditis

• Published in: The journal of clinical endocrinology and metabolism 2017-02, Vol.102 (2), p.672-680
• Main Authors: Vitales-Noyola, Marlen, Ramos-Levi, Ana M, Serrano-Somavilla, Ana, Martínez-Hernández, Rebeca, Sampedro-Nuñez, Miguel, Di Pasquale, Carmelina, González-Amaro, Roberto, Marazuela, Mónica
• Format: Article
• Language: English
• Subjects: Adult; Antigens, CD19; B-Lymphocytes - metabolism; CD19 antigen; CD25 antigen; CD4 antigen; Cell activation; Cell proliferation; Cross-Sectional Studies; Endocrinology; Female; Flow cytometry; Graves Disease - blood; Hashimoto Disease - blood; Humans; Immunofluorescence; Inflammation; Leukocytes (mononuclear); Lymphocytes; Lymphocytes B; Lymphocytes T; Male; Microscopy; Middle Aged; Peripheral blood; Prospective Studies; Signaling Lymphocytic Activation Molecule Family Member 1 - metabolism; T-Lymphocytes, Regulatory - metabolism; Th17 Cells - metabolism; Thyroid; Thyroid gland; Thyroid Gland - metabolism; Thyroiditis
• ISSN: 0021-972X; 1945-7197
• DOI: 10.1210/jc.2016-2322

Signaling lymphocytic activation molecule family 1 (SLAMF1) is a costimulatory receptor expressed by most immune cells. Its role in autoimmune thyroid disease (AITD) is not well known. To analyze the expression and function of the costimulatory receptor SLAMF1 in lymphocytes of patients with AITD. Cross-sectional, prospective, single-center study. Department of Endocrinology, Hospital Universitario de la Princesa, Madrid. Twenty-eight patients with AITD (17 with Graves disease and 11 with Hashimoto thyroiditis) and 21 controls. Multiparametric flow cytometry and immunofluorescence techniques to analyze the expression of SLAMF1 in peripheral blood (n = 28) and thyroid tissue (n = 5) mononuclear cells. Assay of inhibition of cellular proliferation to study the function of SLAMF1 in CD4+CD25+ T regulatory (Treg) cells. Expression levels and the function of SLAMF1 in lymphocytes in AITD patients and controls. Expression of SLAMF1 was significantly increased in peripheral blood CD4+, T helper 17, and CD19+ B cells from AITD patients. Immunofluorescence microscopy detected the presence of SLAMF1+ lymphocytes in thyroid inflammatory cell infiltrate. Functional studies showed that SLAMF1 engagement in Treg cells increased their suppressive function in healthy controls but not in AITD patients. The altered expression of SLAMF1, as well as its defective function observed in patients with AITD, may have a relevant role in the defective immune-regulatory function observed in this condition.