학술논문

Two-year outcome of thymectomy with or without immunosuppressive treatment in nonthymomatous myasthenia gravis and its effect on regulatory T cells.
Document Type
Article
Source
Journal of the Neurological Sciences. Nov2015, Vol. 358 Issue 1/2, p101-106. 6p.
Subject
*THYMOMA
*MYASTHENIA gravis treatment
*AUTOIMMUNE diseases
*THYMECTOMY
*T cells
*SYMPTOMS
*IMMUNOTHERAPY
*PYRIDOSTIGMINE bromide
*THERAPEUTICS
Language
ISSN
0022-510X
Abstract
Background Myasthenia gravis (MG) is the autoimmune disorder in which the thymus is considered the pathogenic organ. Thymectomy (TE) is a therapeutic option for MG and often ameliorates clinical symptoms. Methods We evaluated clinical features and outcomes after TE in patients without thymoma and the influence of TE with or without concomitant immunotherapy on the CD4 + CD25 + regulatory T cell subpopulation of lymphocytes in peripheral blood in defined followed groups of nonthymomatous MG patients. Results A total of 46 patients with generalized MG who underwent transsternal TE were identified. Neurologic outcomes after TE were favorable for the majority of patients mainly from the group treated with corticosteroids or combined immunosuppressive treatment. TEs with immunosuppressive treatment in MG patients were associated with increased percentages of CD4 + CD25 + cells (p < 0.001). No significant change in the postoperative levels of CD4 + CD25 + cells was observed in thymectomized patients who preoperatively only received pyridostigmine. Also their clinical response to TE after 2 years of follow-up was worst of all followed groups. Conclusions The exact mechanism by which TE ameliorates symptoms of MG is yet not clear. These observations indicate that increased percentages of CD4 + CD25 + T cells in MG may be related to disease stability and that TE and synergistic effect with concomitant, continuing immunotherapy augmented the proportion of CD4 + CD25 + T cells. On the basis of our observations TE alone is not enough to increase the number of circulating CD4 + CD25 + regulatory T cells and to establish complete stable remission. [ABSTRACT FROM AUTHOR]