The aim of the study was to estimate the expression of 1 integrin CD49d (very late antigen-4), 2 integrin CD11a (lymphocyte function-associated antigen 1 alpha), L-selectin (CD62L), and intercellular adhesion molecule-1 [ICAM-1 (CD54)] on peripheral blood mononuclear cells in patients with Graves disease (GD) (n ϭ 45, mean age 15.9 Ϯ 5.9 y), in patients with nontoxic nodular goiter (NTNG) (n ϭ 25, mean age 15.2 Ϯ 5.7 y), and in sex-and age-matched healthy control subjects (n ϭ 25, mean age 15.9 Ϯ 2.4 y). The expression of the lymphocyte adhesion molecules was analyzed by the three-color flow cytometry. Decreased percentages of CD49d ϩ and CD11a ϩ lymphocytes were observed in untreated Graves' patients in comparison to healthy controls (p Ͻ 0.007, p Ͻ 0.036) and non-toxic nodular goiter patients (p Ͻ 0.006, p Ͻ 0.019). The analysis of CD62L ϩ and CD54 ϩ antigen expression on peripheral blood lymphocytes revealed increased percentages of L-selectin-and ICAM-1-positive cells in patients with GD (p Ͻ 0.005 for CD62L, p Ͻ 0.008 for ICAM-1) before methimazole therapy, compared with healthy controls. These abnormalities were absent in children with NTNG. In patients with untreated GD, a positive correlation was found between serum levels of free thyroxine and the percentage of CD54 ϩ lymphocytes (r ϭ 0.47, p Ͻ 0.036). GD is an AITD characterized by lymphocytic infiltration of the thyroid gland and the production of TRAb, symporter Na ϩ /I Ϫ , thyroglobulin, and thyroperoxidase antigen (1-3). In addition, literature data underline the role of cytokines and adhesion molecules as new unspecific markers of the autoimmune process in GD (4 -7).Adhesion molecules are the cellular membrane proteins expressed on activated lymphocytes, found to play a pivotal role in the initiation, localization, and perpetuation of thyroid autoimmune disease. They belong to three structurally related families: integrin, Ig supergene, and selectin. Integrins constitute a family of widespread ␣- heterodimeric adhesion receptors that mediate cell attachment to extracellular matrix proteins (fibronectin, laminin, collagen) and cell-cell interactions, which have been grouped in four distinct subfamilies based on -subunit utilization (8