| Literature DB >> 32845010 |
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).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