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Biological Significance of Anti-GH Antibodies in Children Treated with rhGH.
Binder, Gerhard; Heidenreich, Laura; Schnabel, Dirk; Dunstheimer, Desirée; Oeverink, Rudolf; Kiess, Wieland; Körner, Antje; Kratzsch, Jürgen.
Afiliação
  • Binder G; Pediatric Endocrinology, University Children's Hospital, Tübingen, Germany, gerhard.binder@med.uni-tuebingen.de.
  • Heidenreich L; Pediatric Endocrinology, University Children's Hospital, Tübingen, Germany.
  • Schnabel D; Pediatric Endocrinology, Charité, University Medicine, Berlin, Germany.
  • Dunstheimer D; Department of Pediatrics I, Klinikum Augsburg, Augsburg, Germany.
  • Oeverink R; Medicover Oldenburg, Oldenburg, Germany.
  • Kiess W; University Hospital for Children and Adolescents, Leipzig, Germany.
  • Körner A; University Hospital for Children and Adolescents, Leipzig, Germany.
  • Kratzsch J; Institute of Laboratory Medicine, Clinical Chemistry and Molecular Diagnostics, University of Leipzig, Leipzig, Germany.
Horm Res Paediatr ; 91(1): 17-24, 2019.
Article em En | MEDLINE | ID: mdl-30947197
BACKGROUND: The occurrence of antidrug antibodies is common in children treated with recombinant human growth hormone (rhGH). However, their clinical significance is unclear. OBJECTIVE: This study aimed to examine the clinical significance of anti-GH antibodies by analyzing the phenotype of patients who tested positive in relation to the quantity of anti-GH antibodies. METHOD: In this laboratory-based retrospective study encompassing a time span of 6 years, all positive samples were identified, and senders were contacted. Anti-GH antibodies were measured using a radioprecipitation assay; positive samples underwent a confirmatory assay. RESULTS: Out of a total of 104 samples from 66 patients, positive test results were found in 28 samples from 13 patients. Clinical data were available from all but one. The group with positive test results comprised 6 patients with a normal response to GH provocative tests (group A) and 6 with an insufficient response or with isolated GH deficiency (IGHD) type 1A (group B). Diagnoses in group A were neurosecretory dysfunction, bioinactive GH syndrome and constitutional delay of growth and puberty. Diagnoses in group B were IGHD type 1A, septo-optic dysplasia, and cerebral midline defect with multiple pituitary hormone deficiency. Insufficient growth response to rhGH was absent except in one sibling pair with IGHD type 1A and a patient with cerebral midline defect. These patients had the highest concentrations of anti-GH antibodies. CONCLUSIONS: The biological significance of anti-GH antibodies seems to be limited to patients with high concentrations of anti-GH antibodies. For all other patients, we recommend a careful "wait and see" strategy and monitoring antibody titers.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hormônio do Crescimento Humano / Nanismo Hipofisário / Anticorpos Tipo de estudo: Observational_studies / Prognostic_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Horm Res Paediatr Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Hormônio do Crescimento Humano / Nanismo Hipofisário / Anticorpos Tipo de estudo: Observational_studies / Prognostic_studies Limite: Child / Child, preschool / Female / Humans / Infant / Male Idioma: En Revista: Horm Res Paediatr Ano de publicação: 2019 Tipo de documento: Article