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贾第虫病和常见可变免疫缺陷患者的发病率、管理经验及特征

Incidence, Management Experience and Characteristics of Patients with Giardiasis and Common Variable Immunodeficiency.

作者信息

Díaz-Alberola Irene, Gutiérrez-Bautista Juan Francisco, Espuch-Oliver Andrea, García-Aznar José María, Anderson Per, Jiménez Pilar, Hidalgo-Tenorio Carmen, López-Nevot Miguel Ángel

机构信息

Servicio de Análisis Clínicos e Inmunología, Hospital Universitario Virgen de las Nieves, 18014 Granada, Spain.

Programa de Doctorado en Biomedicina, University of Granada, 10816 Granada, Spain.

出版信息

J Clin Med. 2022 Nov 27;11(23):7007. doi: 10.3390/jcm11237007.

Abstract

Common variable immunodeficiency (CVID) is an antibody immunodeficiency with a wide variety of clinical and immunological manifestations, and whose genetic cause is found in about 25% of diagnosed cases. is one of the main causes of gastrointestinal infections in CVID. 5-Nitroimidazoles are the most used first-line treatment, but nitroimidazole-refractory giardiasis is increasing. Nevertheless, only a few cases of refractory giardiasis in CVID have been reported. This study aimed to determine the incidence of infection in our CVID cohort, shows our management experience and describes patients' phenotypic features. Clinical data collection, immunological, immunogenetics and microbiology assays were performed, and previous cases of giardiasis in CVID were reviewed. The incidence of symptomatic giardiasis was 12.9%. The main immunological features were undetectable or decreased IgA levels and reduced switched memory B cells. A probable pathogenic variant was detected in one. Three patients responded to metronidazole but suffered reinfections, and one was a refractory giardiasis eradicated with innovative quinacrine plus paromomycin combination. This work could contribute to the decision-making and therapeutic management of future patients with CVID and giardiasis, highlighting the importance of the early detection and treatment of infections in patients with CVID to ensure a good quality of life.

摘要

普通可变免疫缺陷(CVID)是一种具有多种临床和免疫表现的抗体免疫缺陷疾病,约25%的确诊病例可发现其遗传病因。[此处原文缺失一个主语,暂按原文翻译]是CVID患者胃肠道感染的主要原因之一。5-硝基咪唑类药物是最常用的一线治疗药物,但硝基咪唑难治性贾第虫病的发生率正在上升。尽管如此,CVID患者中难治性贾第虫病的报道仅少数几例。本研究旨在确定我们CVID队列中[此处原文缺失一个病原体名称,暂按原文翻译]感染的发生率,展示我们的管理经验并描述患者的表型特征。我们进行了临床数据收集、免疫学、免疫遗传学和微生物学检测,并回顾了CVID患者既往的贾第虫病病例。有症状的贾第虫病发生率为12.9%。主要免疫特征为无法检测到或IgA水平降低以及转换记忆B细胞减少。在其中一例中检测到一个可能的[此处原文缺失一个致病相关的词汇,暂按原文翻译]致病变异。三名患者对甲硝唑有反应,但遭受了再次感染,一名难治性贾第虫病患者通过创新的喹吖因加巴龙霉素联合用药得以根除。这项工作有助于未来CVID和贾第虫病患者的决策制定和治疗管理,强调了早期检测和治疗CVID患者感染以确保良好生活质量的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7a6b/9740678/ea5687c3b0b5/jcm-11-07007-g001.jpg

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