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原发性抗体缺陷症的治疗和管理:德国跨学科循证共识指南。

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

机构信息

Institute for Medical Immunology, Charité Universitaetsmedizin Berlin, Berlin, Germany.

Department of Paediatric Pulmonology, Allergy and Neonatology, Hannover Medical School, Hannover, Germany.

出版信息

Eur J Immunol. 2020 Oct;50(10):1432-1446. doi: 10.1002/eji.202048713. Epub 2020 Sep 9.

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).

摘要

本循证临床指南为原发性抗体缺陷症(PAD)患者的治疗和护理提供了共识建议。指南小组由德国、瑞士和奥地利医疗保健系统的 20 个临床和科学专业协会以及患者代表组成。建议基于系统文献检索、数据提取以及方法学和研究质量评估的结果,结合相关代表的临床专业知识。通过名义小组技术确定基于共识的建议。PAD 是临床上最重要的原发性免疫缺陷组之一。大多数 PAD 患者易感染,但免疫失调、自身免疫和癌症也影响着大量患者,且可能先于感染发生。因此,本指南涵盖了感染(例如抗生素预防、支气管扩张症的管理)和非感染性表现(例如肉芽肿病、免疫性血细胞减少症的管理)的跨学科临床和治疗方面。将 PAD 分为具有明确、可能、可能或不太可能获益的 IgG 替代治疗的疾病实体。提供了 IgG 替代治疗的治疗指征、剂量、给药途径和不良反应的总结和共识建议。还强调了同时存在的 T 细胞功能受损的特殊方面,以及以前归类为 PAD 的某些单基因先天性免疫缺陷(APDS、CTLA-4- 和 LRBA 缺陷)的临床数据。

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