| Literature DB >> 31594658 |
Claire Mj Lefeuvre1, Cloé A Payet1, Odessa-Maud Fayet1, Solène Maillard1, Frédérique Truffault1, Vincent Bondet2, Darragh Duffy2, Vincent de Montpreville3, Maria-Rosa Ghigna3, Elie Fadel3, Audrey Mansuet-Lupo4, Marco Alifano4, Pierre Validire5, Dominique Gossot5, Anthony Behin6, Bruno Eymard6, Sonia Berrih-Aknin1, Rozen Le Panse7.
Abstract
Thymomas are associated with a very high risk of developing Myasthenia Gravis (MG). Our objectives were to identify histological and biological parameters to allow early diagnosis of thymoma patients susceptible to developing MG. We conducted a detailed retrospective analysis from a patient database, searching for differences between patients with thymoma-associated MG (MGT, n = 409) and thymoma without MG (TOMA, n = 111) in comparison with nonthymomatous MG patients (MG, n = 1246). We also performed multiplex and single molecule arrays to measure the serum levels of cytokines in these groups of patients and controls (n = 14-22). We identified a set of parameters associated with MG development in thymoma patients: 1) detection of anti-acetylcholine receptor (AChR) antibodies, 2) development of B1 or B2 thymoma subtypes, 3) presence of ectopic thymic germinal centers (GCs), 4) local invasiveness of thymoma, and 5) being a woman under 50 years old. Among these parameters, 58.8% of MGT patients displayed GCs with a positive correlation between the number of GCs and anti-AChR titers. By immunohistochemistry, we found thymic GCs in the adjacent tissues of thymomas encircled by high endothelial venules (HEVs) that could favor peripheral cell recruitment. We also clearly associated MG symptoms with higher IFN-γ, IL-1β and sCD40L serum levels, specifically in MGT patients compared to TOMA patients. Altogether, these analyses allowed the clear identification of histological, in particular the presence of GCs, and biological parameters that would facilitate the evaluation of the probability of the MG outcome postoperatively in thymoma patients.Entities:
Keywords: Autoimmune diseases; Cytokines; Myasthenia gravis; Paraneoplastic syndromes; Tertiary lymphoid structures; Thymus
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Year: 2019 PMID: 31594658 DOI: 10.1016/j.jaut.2019.102337
Source DB: PubMed Journal: J Autoimmun ISSN: 0896-8411 Impact factor: 7.094