Treatment of severe aplastic anemia with cyclosporin-a and high-dose methylprednisolone
Abstract
15 patients with severe aplastic anemia were treated with an immunosuppresive regimen consisting of Cyclosporin-A(CsA) and highdose méthylprednisolone (HMP). Initially CsA was given orally at a dosage of 10 mg/kg/day and monitoring the serum level of the drug, blood levels of 200-500 ng/ml were maintained thereafter. CsA treatment was continued at least 3 months at which time the treatment was terminated in unresponsive patients depending on the peripheral cell counts. HMP was administered simultaneously with CsA at 30 mg/kg/day IV for 3 days, 20 mg/kg/day IV for 3 days and 10 mg/kg/day IV for 4 days. Within 3 months improvement of hematopoiesis was seen in 6 patients (40 %). First signs of response were seen in 21-69 (34) days. This was followed by complete remission in 3 patients, partial remission in 2 patients and minimal improvement in 1 patient. Remissions were proved to be dependent on the continued administration of CsA. Sequential changes of T-cell subsets using APAAP method revealed an increasing ratio of T-helper cells to T-suppressor cells. This Observation strongly suggests the role of T-cells in the pathogenesis of some cases of aplastic anemia.
Keywords
References
- Alter BP. The bone marrow failure syndroms. In: nathan OD. Oski FA (eds). Hematology of Infancy and Childhood. 3rd ed. Philadelphia: WB Saunders Company 1987.
Details
Primary Language
English
Subjects
Clinical Sciences
Journal Section
Research Article
Authors
N. Üskent
This is me
Türkiye
M. Danacı
This is me
Türkiye
M. Özel
This is me
Türkiye
M. Yaylacı
This is me
Türkiye
H. Tor
This is me
Türkiye
Publication Date
January 1, 1992
Submission Date
October 13, 2016
Acceptance Date
October 1, 1991
Published in Issue
Year 1992 Volume: 5 Number: 1