Anti-factor H autoantibody-associated hemolytic uremic syndrome in an Argentine pediatric cohort

Author:

Dos Santos Célia1ORCID,Trinidad Jesica1,Castera Santiago2,Alconcher Laura3ORCID,Coccia Paula Alejandra4ORCID,Manni Federico Javie5ORCID,Alberto María Fabiana2,Sánchez-Luceros Analía6ORCID

Affiliation:

1. Laboratorio de Hemostasia y Trombosis, Instituto de Medicina Experimental-CONICET-Academia Nacional de Medicina, Ciudad Autónoma de Buenos Aires C1425AUM, Argentina

2. Instituto de Investigaciones Hematológicas “Mariano R. Castex”, Academia Nacional de Medicina, Ciudad Autónoma de Buenos Aires C1425AUM, Argentina

3. Unidad de Nefrología Pediátrica, Hospital Interzonal General Dr José Penna, Bahia Blanca, Provincia de Buenos Aires B8000, Argentina

4. Servicio de Nefrología Pediátrica, Hospital Italiano, Ciudad Autónoma de Buenos Aires C1199, Argentina

5. Servicio de Hematología, Hospital de Niños “Dr. Orlando Alassia”, Santa Fe, Provincia de Santa Fe 3000, Argentina

6. Laboratorio de Hemostasia y Trombosis, Instituto de Medicina Experimental-CONICET-Academia Nacional de Medicina, Ciudad Autónoma de Buenos Aires C1425AUM, Argentina; Instituto de Investigaciones Hematológicas “Mariano R. Castex”, Academia Nacional de Medicina, Ciudad Autónoma de Buenos Aires C1425AUM, Argentina

Abstract

Aim: To describe the clinical characteristics and frequency of anti-factor H (FH) autoantibody-associated atypical hemolytic uremic syndrome (aHUS) in the first cohort of Argentine patients. Methods: The presence of anti-FH autoantibodies in 70 pediatric patients with suspected aHUS was investigated between 2013 and 2022. Clinical and laboratory parameters were collected and compared between patients who were positive and negative for anti-FH antibodies. Results: The 70 patients screened for anti-FH autoantibodies presented clinical features of non-immune microangiopathic hemolytic anemia, thrombocytopenia and renal injury. Positive titers were found in 14 children [mean: 1,938 arbitrary units per mL (AU/mL), range 179–8,500]. Due to missing clinical data, two patients who tested positive for anti-FH and 20 patients who tested negative for anti-FH were excluded from the data analysis. The laboratory features and clinical manifestations of anti-FH-positive aHUS cases (n = 12) were very similar to those of subjects with no autoantibodies detected (n = 36). Treatment administration was heterogeneous among the 12 patients analyzed. Dialysis was performed in six patients in total. Five children received plasmapheresis, while three patients were treated with plasma exchange followed by administration of eculizumab. Two patients received eculizumab only and one showed significant improvement solely through supportive care. Eight patients in total received immunosuppressive therapy. Follow-up of three patients showed a significant decrease of anti-FH autoantibody titers in 2/3 after treatment and during clinical remission. Conclusions: The cohort of 70 pediatric patients in this study demonstrated that the frequency of anti-FH autoantibody-associated aHUS in Argentina is 20%. The implementation of anti-FH testing in the country can potentially contribute to improved treatment and follow-up for patients with autoimmune aHUS.

Publisher

Open Exploration Publishing

Subject

General Medicine

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