INFLUENCE OF FK-506 (TACROLIMUS) ON CIRCULATING CD4(-CELLS EXPRESSINGCD25 AND CD45RA ANTIGENS IN 19 PATIENTS WITH CHRONIC PROGRESSIVE MULTIPLE-SCLEROSIS PARTICIPATING IN AN OPEN-LABEL DRUG SAFETY TRIAL() T)

We have taken the opportunity of a clinical trial of the potential eff icacy and safety of FK 506 (tacrolimus) in chronic progressive multipl e sclerosis (MS) to examine the influence of this potent new immunosup pressant on circulating T-lymphocytes in an otherwise healthy non-tran splant population. Peripheral blood levels of subsets of CD4(+) T lymp hocytes expressing the activation molecule interleukin-2 receptor (p55 a chain; CD25) or the CD45RA isoform were determined sequentially in 19 patients that were treated continuously with oral FK 506 (starting dose 0.15 mg/kg/day) for 12 months. No significant change in the propo rtion of circulating CD25(+) CD4(+) cells was observed over the study period in which the mean trough plasma FK 506 level rose from 0.3 +/- 0.2 to 0.5 +/- 0.4 ng/ml. There was also no significant effect of FK 5 06 on the percentage of CD45RA(+) CD4(+) cells in the peripheral blood at 12 months compared with pretreatment values. Analysis of a subgrou p of 7 patients, who showed a sustained reduction in CD25(+) CD4(+) ce lls and a reciprocal increase in CD45RA(+) CD4(+) cells for at least 6 months after start of treatment, did not reveal any difference in dis ability at one year compared with the treatment group as a whole. The side effects of FK 506 were mild and the overall degree of disability estimated by the mean Kurtzke expanded disability status scale (EDSS) score or the ambulation index did not deteriorate significantly in the 19 patients studied over the 12 months of FK 506 administration.