Raúl F Reyes-Huerta, Vladimir Mandujano-López, Guadalupe Velásquez-Ortiz, Beatriz Alcalá-Carmona, María J Ostos-Prado, Yatzil Reyna-Juárez, David E Meza-Sánchez, Guillermo Juárez-Vega, Nancy R Mejía-Domínguez, Jiram Torres-Ruiz, Diana Gómez-Martin, José L Maravillas-Montero
Idiopathic inflammatory myopathies are a heterogeneous group of rare autoimmune disorders characterized by progressive muscle weakness and the histopathologic findings of inflammatory infiltrates in muscle tissue. Although their pathogenesis remains indefinite, the association of autoantibodies with clinical manifestations and the evidence of high effectiveness of depleting therapies suggest that B cells could be implicated. Therefore, we explored the landscape of peripheral B cells in this disease by multiparametric flow cytometry, finding significant numerical decreases in memory and double negative subsets, as well as an expansion of the naïve compartment relative to healthy controls, that contribute to defining disease-associated B cell subset signatures and correlating with different clinical features of patients...
March 30, 2024: Journal of Leukocyte Biology