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X-Linked Agammaglobulinaemia: Outcomes in the modern era

Journal

CLINICAL IMMUNOLOGY
Volume 183, Issue -, Pages 54-62

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.clim.2017.07.008

Keywords

XLA; X-Linked Agammaglobulinaemia; Immunoglobulin; Bronchiectasis; Immune deficiency

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Colonel Ogden Bruton reported X-Linked Agammaglobulinaemia in 1952 and treated the child with replacement immunoglobulin therapy. Over 60 years later, the treatment for XLA has largely remained unchanged. Replacement immunoglobulin lacks the isotypes IgA and IgM, leading to concerns that patients continue to experience recurrent sinopulmonary tract infections and be at increased risk of bronchiectasis. There is potential hope of earlier diagnosis with newborn screening, and a potential cure for these patients, in the form of gene therapy. However, it is first necessary to evaluate current management and outcomes to aid decisions regarding further research and clinical trials. This article reviews current management and outcomes of XLA, whilst identifying gaps in our knowledge base that may need answering before we proceed with novel diagnostic methods and treatment for XLA. (C) 2017 Elsevier Inc. All rights reserved.

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