Molecular dissection of human B-cell tolerance – insights from patients with rare genetic diseases | ResearchHub
Enriched recordOpen access
Molecular dissection of human B-cell tolerance – insights from patients with rare genetic diseases
Henner Morbach, Greta Meyers, Yen-Shing Ng, Jean‐Nicolas Schickel, Laurence C. Menard, Sergei Rudchenko, Jessica Lineth Rojas, Charlotte Cunningham‐Rundles, Mary Ellen Conley, İsmail Reisli, José Luis Franco, Eric Meffre
Open the manuscript using the link above. DOC files open in Word or a compatible document reader.
Abstract
B cells play a central role in the pathogenesis of many autoimmune diseases. Therefore, understanding the mechanisms that regulate B-cell tolerance in humans is important for the development of new therapeutic strategies. Patients with monogenic diseases provide rare opportunities to study the impact of specific gene mutations on the regulation of human B cell tolerance. By this, we could show that alterations in B-cell receptor and Toll-like receptor (TLR) signaling pathways result in defective central B-cell tolerance.
