Literature DB >> 32845010

Treatment and management of primary antibody deficiency: German interdisciplinary evidence-based consensus guideline.

Leif Hanitsch1, Ulrich Baumann2, Kaan Boztug3, Ulrike Burkhard-Meier4, Maria Fasshauer5, Pirmin Habermehl6, Fabian Hauck7, Gerd Klock8, Johannes Liese9, Oliver Meyer10, Rainer Müller11, Jana Pachlopnik-Schmid12, Dorothea Pfeiffer-Kascha13, Klaus Warnatz14,15, Claudia Wehr15,16, Kirsten Wittke1, Tim Niehues17, Horst von Bernuth18,19,20.   

Abstract

This evidence-based clinical guideline provides consensus-recommendations for the treatment and care of patients with primary antibody deficiencies (PADs). The guideline group comprised 20 clinical and scientific expert associations of the German, Swiss, and Austrian healthcare system and representatives of patients. Recommendations were based on results of a systematic literature search, data extraction, and evaluation of methodology and study quality in combination with the clinical expertise of the respective representatives. Consensus-based recommendations were determined via nominal group technique. PADs are the largest clinically relevant group of primary immunodeficiencies. Most patients with PADs present with increased susceptibility to infections, however immune dysregulation, autoimmunity, and cancer affect a significant number of patients and may precede infections. This guideline therefore covers interdisciplinary clinical and therapeutic aspects of infectious (e.g., antibiotic prophylaxis, management of bronchiectasis) and non-infectious manifestations (e.g., management of granulomatous disease, immune cytopenia). PADs are grouped into disease entities with definitive, probable, possible, or unlikely benefit of IgG-replacement therapy. Summary and consensus-recommendations are provided for treatment indication, dosing, routes of administration, and adverse events of IgG-replacement therapy. Special aspects of concomitant impaired T-cell function are highlighted as well as clinical data on selected monogenetic inborn errors of immunity formerly classified into PADs (APDS, CTLA-4-, and LRBA-deficiency).
© 2020 The Authors. European Journal of Immunology published by Wiley-VCH GmbH.

Entities:  

Keywords:  CVID; autoimmunity; hypogammaglobulinemia; immunoglobulins; primary antibody deficiency

Year:  2020        PMID: 32845010     DOI: 10.1002/eji.202048713

Source DB:  PubMed          Journal:  Eur J Immunol        ISSN: 0014-2980            Impact factor:   5.532


  5 in total

1.  Case Report: Whole-Genome Sequencing of Serially Collected Haemophilus influenzae From a Patient With Common Variable Immunodeficiency Reveals Within-Host Evolution of Resistance to Trimethoprim-Sulfamethoxazole and Azithromycin After Prolonged Treatment With These Antibiotics.

Authors:  Paul Christoffer Lindemann; Haima Mylvaganam; Oddvar Oppegaard; Inger Lill Anthonisen; Nermin Zecic; Dagfinn Skaare
Journal:  Front Cell Infect Microbiol       Date:  2022-06-01       Impact factor: 6.073

Review 2.  Genetic Predisposition and the Variable Course of Infectious Diseases.

Authors:  Axel Schmidt; Ana M Groh; Julia S Frick; Maria J G T Vehreschild; Kerstin U Ludwig
Journal:  Dtsch Arztebl Int       Date:  2022-02-25       Impact factor: 8.251

Review 3.  Future of Therapy for Inborn Errors of Immunity.

Authors:  Elena Perez
Journal:  Clin Rev Allergy Immunol       Date:  2022-01-12       Impact factor: 10.817

4.  The Immune Deficiency and Dysregulation Activity (IDDA2.1 'Kaleidoscope') Score and Other Clinical Measures in Inborn Errors of Immunity.

Authors:  Markus G Seidel; Victoria K Tesch; Linlin Yang; Fabian Hauck; Anna Lena Horn; Maria Anna Smolle; Franz Quehenberger; Martin Benesch
Journal:  J Clin Immunol       Date:  2021-11-19       Impact factor: 8.542

5.  Impact of COVID-19 pandemic on EJI and the extended immunological community.

Authors:  James Di Santo
Journal:  Eur J Immunol       Date:  2021-01       Impact factor: 5.532

  5 in total

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