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      Bronchiectasis in Primary Antibody Deficiencies: A Multidisciplinary Approach

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          Abstract

          Bronchiectasis, the presence of bronchial wall thickening with airway dilatation, is a particularly challenging complication of primary antibody deficiencies. While susceptibility to infections may be the primary factor leading to the development of bronchiectasis in these patients, the condition may develop in the absence of known infections. Once bronchiectasis is present, the lungs are subject to a progressive cycle involving both infectious and non-infectious factors. If bronchiectasis is not identified or not managed appropriately, the cycle proceeds unchecked and yields advanced and permanent lung damage. Severe symptoms may limit exercise tolerance, require frequent hospitalizations, profoundly impair quality of life (QOL), and lead to early death. This review article focuses on the appropriate identification and management of bronchiectasis in patients with primary antibody deficiencies. The underlying immune deficiency and the bronchiectasis need to be treated from combined immunology and pulmonary perspectives, reflected in this review by experts from both fields. An aggressive multidisciplinary approach may reduce exacerbations and slow the progression of permanent lung damage.

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          Most cited references80

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          Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification

          Since 2013, the International Union of Immunological Societies (IUIS) expert committee (EC) on Inborn Errors of Immunity (IEI) has published an updated phenotypic classification of IEI, which accompanies and complements their genotypic classification into ten tables. This phenotypic classification is user-friendly and serves as a resource for clinicians at the bedside. There are now 430 single-gene IEI underlying phenotypes as diverse as infection, malignancy, allergy, autoimmunity, and autoinflammation. We herein report the 2019 phenotypic classification, including the 65 new conditions. The diagnostic algorithms are based on clinical and laboratory phenotypes for each of the ten broad categories of IEI.
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            Practice parameter for the diagnosis and management of primary immunodeficiency.

            The American Academy of Allergy, Asthma & Immunology (AAAAI) and the American College of Allergy, Asthma & Immunology (ACAAI) have jointly accepted responsibility for establishing the "Practice parameter for the diagnosis and management of primary immunodeficiency." This is a complete and comprehensive document at the current time. The medical environment is a changing environment, and not all recommendations will be appropriate for all patients. Because this document incorporated the efforts of many participants, no single individual, including those who served on the Joint Task Force, is authorized to provide an official AAAAI or ACAAI interpretation of these practice parameters. Any request for information about or an interpretation of these practice parameters by the AAAAI or ACAAI should be directed to the Executive Offices of the AAAAI, the ACAAI, and the Joint Council of Allergy, Asthma & Immunology. These parameters are not designed for use by pharmaceutical companies in drug promotion.
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              British Thoracic Society Guideline for bronchiectasis in adults

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                Author and article information

                Contributors
                Journal
                Front Immunol
                Front Immunol
                Front. Immunol.
                Frontiers in Immunology
                Frontiers Media S.A.
                1664-3224
                31 March 2020
                2020
                : 11
                : 522
                Affiliations
                [1] 1Division of Allergy Immunology, Department of Pediatrics, Louisiana State University Health Sciences Center New Orleans , New Orleans, LA, United States
                [2] 2Children's Hospital of New Orleans , New Orleans, LA, United States
                [3] 3Division of Pulmonology and Sleep Medicine, Department of Pediatrics, Massachusetts General Hospital, Harvard Medical School , Boston, MA, United States
                Author notes

                Edited by: Giuseppe Spadaro, University of Naples Federico II, Italy

                Reviewed by: Cinzia Milito, Sapienza University of Rome, Italy; Anna Sediva, University Hospital in Motol, Czechia

                *Correspondence: Luke A. Wall lwall@ 123456lsuhsc.edu

                This article was submitted to Primary Immunodeficiencies, a section of the journal Frontiers in Immunology

                Article
                10.3389/fimmu.2020.00522
                7138103
                32296433
                3a83497d-cfe1-4080-a1ec-0b46cce0321d
                Copyright © 2020 Wall, Wisner, Gipson and Sorensen.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 18 October 2019
                : 06 March 2020
                Page count
                Figures: 5, Tables: 1, Equations: 0, References: 119, Pages: 15, Words: 11426
                Categories
                Immunology
                Review

                Immunology
                bronchiectasis,antibody deficiencies,primary immunodeficencies (pid),immunoglobulin replacement therapy (igrt),pulmonary therapy,non-infectious complications

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