AI Article Synopsis

  • * Recent studies indicate that abnormal processes in the thymus contribute significantly to MG, particularly in patients with anti-acetylcholine receptor antibodies, highlighting the importance of thymectomy in reducing harmful antibody-producing B cells.
  • * While thymectomy is not advisable for all MG patients, especially those without specific antibodies, it can help reduce self-reactive T cells in patients with a thymoma; further research is needed to fully understand the immune mechanisms involved.

Article Abstract

Myasthenia gravis (MG) is an autoimmune disease mediated by autoantibodies to the striated muscle tissue. It is often treated by thymectomy. We review recent studies to investigate the biological implications of thymectomy. In anti-acetylcholine receptor antibody (anti-AchR Ab)-positive patients without a thymoma, abnormal germinal center formation in the thymus seems to play an essential role in the pathogenesis of MG. Specific differentiation of B cells producing anti-AchR Ab takes place uniquely in the thymus, and thymectomy is thought to assist in terminating the provision of high-affinity anti-AchR antibody-producing cells to peripheral organs. Thymectomy is not indicated for anti-AchR Ab-negative MG patients who are antimuscle specific kinase antibody (anti-MuSK Ab)-positive, although some anti-MuSK Ab-negative patients may benefit from the procedure. A thymoma can be considered as an acquired thymus with insufficient function of negative selection. The resection of a thymoma is thought to terminate the production of self-reactive T cells. Thus, the biological implications of thymectomy for MG have been partially revealed. Nevertheless, additional studies are needed to elucidate the ontogeny of T cells that recognize AchR and the mechanism of the activation of anti-AchR antibodies producing B cells.

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http://dx.doi.org/10.1007/s00595-009-4134-2DOI Listing

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