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- Title
Immunosuppressive Therapy of Antibody-Mediated aHUS and TTP.
- Authors
Kelen, Kata; Horváth, Orsolya; Kis, Éva; Mikes, Bálint; Sallay, Péter; Prohászka, Zoltán; Szabó, Attila József; Reusz, György S.
- Abstract
The recent classification of pediatric thrombotic microangiopathies (TMA) takes into consideration mechanisms of disease for guidance to targeted therapies. We present our experience with seven patients with antibody mediated atypical hemolytic uremic syndrome (aHUS) and thrombotic thrombocytopenic purpura (TTP). Five children had aHUS with antibodies against complement factor H (CFH-ab) and two with TTP with antibodies against metalloproteinase ADAMTS13. In the aHUS cases diagnosed and treated before the eculizumab era, CFH-ab was detected using the ELISA assay. Mutational analysis of selected complement genes was performed. TTP was diagnosed if, in addition to microangiopathic hemolytic anemia and thrombocytopenia, ischemic organ involvement and severe deficiency in ADAMTS13 activity were present. Treatment protocol consisted of plasma exchanges (PE) and steroid pulses, followed by the combination of cyclophosphamide and rituximab to achieve long-term immunosuppression. Four patients with CFH-ab and the TTP patients with ADAMTS13 antibodies came into sustained remission. After a median follow-up of 11.7 (range 7.7–12.9) years without maintenance therapy, no disease recurrence was observed; nevertheless, six patients, two had hypertension and two had proteinuria as a late consequence. One patient, with late diagnosis of CFH-ab and additional genetic risk factors who was treated only with PE and plasma substitution, reached end-stage renal disease and was later successfully transplanted using eculizumab prophylaxis. In the cases of antibody-mediated TMAs, PE and early immunosuppressive treatment may result in sustained remission with preserved kidney function. Further data are needed to establish optimal treatment of anti-FH antibody-associated HUS.
- Subjects
COMPLEMENT factor H; IMMUNOSUPPRESSIVE agents; THROMBOTIC thrombocytopenic purpura; HEMOLYTIC-uremic syndrome; THROMBOTIC microangiopathies; RITUXIMAB
- Publication
International Journal of Molecular Sciences, 2023, Vol 24, Issue 18, p14389
- ISSN
1661-6596
- Publication type
Article
- DOI
10.3390/ijms241814389