Fig. 2. Activation state of Faslo and Fashi thymocytes. Freshly isolated thymocytes were stained with anti-Fas antibody and PE-labeled anti-CD25 or FITC-labeled anti-HLA-DR. (A) In Fas expression analysis, gates were set to define Faslo and Fashi thymocytes. During the acquisition step, events were accumulated in these gates. Analysis of one representative MG patient (anti-AChR antibody titer 33 nmol/L) is shown. In this representative analysis (one of six experiments) the percentage of HLA-DR–expressing or CD25-expressing cells is strikingly higher in Fashi thymocytes than in Faslo thymocytes. (B) Such analyses were performed on 6 controls and 6 MG patients. Data presented are mean ± SEM. The increase in HLA-DR or CD25+ cells in Fashi thymocytes compared with Faslo thymocytes were similar in controls and in MG patients.
Fig. 2.

Activation state of Faslo and Fashi thymocytes. Freshly isolated thymocytes were stained with anti-Fas antibody and PE-labeled anti-CD25 or FITC-labeled anti-HLA-DR. (A) In Fas expression analysis, gates were set to define Faslo and Fashi thymocytes. During the acquisition step, events were accumulated in these gates. Analysis of one representative MG patient (anti-AChR antibody titer 33 nmol/L) is shown. In this representative analysis (one of six experiments) the percentage of HLA-DR–expressing or CD25-expressing cells is strikingly higher in Fashi thymocytes than in Faslo thymocytes. (B) Such analyses were performed on 6 controls and 6 MG patients. Data presented are mean ± SEM. The increase in HLA-DR or CD25+ cells in Fashi thymocytes compared with Faslo thymocytes were similar in controls and in MG patients.

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