The pathogenesis of primary biliary cirrhosis Patogénesis en cirrosis biliar primaria

• Main Authors: J. A. Solís Herruzo, P. Solís Muñoz, T. Muñoz Yagüe
• Format: Article
• Language: English
• Published: Aran Ediciones 2009-06-01
• Series: Revista Espanola de Enfermedades Digestivas
• Subjects: Primary biliary cirrhosis; Pathogenesis; Autoimmunity; Xenobiotics; Genetics
• Online Access: http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S1130-01082009000600007

Primary biliary cirrhosis (PBC) would develop when the immune system comes across a microorganism with proteins similar to those in the piruvate dehydrogenase complex E2 (PDC-E2), or a neoantigen resulting from a xenobiotic-modified autoantigen. This would lead to an innate immune response where TLRs would play a pivotal mediating role, which would give rise to a local microenvironment favoring an adaptive immune response. Such response would be particularly strong in individuals with selected genetic characteristics. The genetic characteristics underlying this predisposition remain unknown, but they likely entail small numbers of scarcely-active regulatory T cells. The AE2 anion exchanger, which is deficient in patients with PBC, may reduce the number and activity of regulatory T cells. NK cells are also pivotal in the preparation of an adaptive response, as they release a number of cytokines and chemokines that favor and recruit antigen-presenting cells to activate B and T cells - CD4+ Th1 and CD8+. An activation of the former would increase the production of IgM and anti-mitochondrial IgG and IgA antibodies against PDC-E2. An activation of CD8+ cells, also sensitive to PDC-2 as aberrantly expressed on the surface of BECs and SECs, would result in apoptosis for these epithelial cells, and in small bile-duct destruction. Immune response is likely inadequately suppressed because of the small numbers of scarcely-active regulatory T cells, the latter resulting from low genetic expression and activity of the AE2 transporter.