| Literature DB >> 18644699 |
Shinji Shimoda1, Hiroshi Miyakawa, Minoru Nakamura, Hiromi Ishibashi, Kentaro Kikuchi, Hiroto Kita, Hiroaki Niiro, Youjirou Arinobu, Nobuyuki Ono, Ian R Mackay, M Eric Gershwin, Koichi Akashi.
Abstract
Approximately 5% of patients with primary biliary cirrhosis (PBC) lack characteristic anti-mitochondrial antibodies (AMA). Yet clinically AMA+ and AMA- patients are similar. Using both AMA+ and AMA- patients, we quantitated the frequency of autoreactive T cells that respond to the major CD4 T-cell epitope, PDC-E2 163-176, using limiting dilution assays and quantitation of IFN-gamma, IL-10 and IL-4. Further, based on data that both PBC patients and healthy subjects have CD4+ T cells that recognize PDC-E2 163-176 but with differing costimulation requirements, assays were performed using two different antigen-presenting cell (APC) systems: either autologous peripheral blood mononuclear cells (PBMC) or HLA DR53 transfected mouse fibroblast cell lines (L-DR53). When costimulation-incompetent L-DR53 were used as APCs, the PDC-E2 CD4 T-cell frequency and capacity for IFN-gamma production were equivalent in both AMA+ and AMA- patients but the frequencies of such cells were significantly lower in normals, with IL-10 production similar in all three groups. Thus, in PBC there is 'universal' autoreactive CD4+ T-cell immune responsiveness to the critical autoantigen, PDC-E2. These observations emphasize that the mitochondrial autoreactivity in PBC is a multi-lineage response and hence, AMA-negative PBC may be an anachronism that refers only to sera autoantibodies.Entities:
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Year: 2008 PMID: 18644699 DOI: 10.1016/j.jaut.2008.05.003
Source DB: PubMed Journal: J Autoimmun ISSN: 0896-8411 Impact factor: 7.094