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Development of high sustained anti-drug antibody titers and corresponding clinical decline in a late-onset Pompe disease patient after 11+ years on enzyme replacement therapy.
Kim, Katherine H; Desai, Ankit K; Vucko, Erika R; Boggs, Tracy; Kishnani, Priya S; Burton, Barbara K.
Afiliación
  • Kim KH; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Division of Genetics, Genomics and Metabolism, Ann & Robert H Lurie Children's Hospital of Chicago, 225 E Chicago Ave Box 59, Chicago, IL 60611, USA.
  • Desai AK; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Box 103856 DUM, Durham, NC 27710, USA.
  • Vucko ER; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Division of Genetics, Genomics and Metabolism, Ann & Robert H Lurie Children's Hospital of Chicago, 225 E Chicago Ave Box 59, Chicago, IL 60611, USA.
  • Boggs T; Department of Rehabilitation Services, Duke University Health System, 234 Crooked Creek Pkwy, Suite 310, Durham, NC 27713, USA.
  • Kishnani PS; Division of Medical Genetics, Department of Pediatrics, Duke University Medical Center, Box 103856 DUM, Durham, NC 27710, USA.
  • Burton BK; Department of Pediatrics, Northwestern University Feinberg School of Medicine, Division of Genetics, Genomics and Metabolism, Ann & Robert H Lurie Children's Hospital of Chicago, 225 E Chicago Ave Box 59, Chicago, IL 60611, USA.
Mol Genet Metab Rep ; 36: 100981, 2023 Sep.
Article en En | MEDLINE | ID: mdl-37342670
ABSTRACT
A late-onset Pompe disease patient developed high sustained antibody titers (HSAT) of ≥51,200 after 11+ years on alglucosidase alfa and previous tolerance. There was a corresponding worsening of motor function and rise in urinary glucose tetrasaccharide (Glc4). Following immunomodulation therapy, HSAT were eliminated with improved clinical outcomes and biomarker trends. This report highlights the importance of continued surveillance of antibody titers and biomarkers, the negative impact of HSAT, and improved outcomes with immunomodulation therapy.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Mol Genet Metab Rep Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Mol Genet Metab Rep Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos
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