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Inhibits in Co-culture: Implications of a Mutually Antagonistic Relationship on Virulence and Inflammation in the CF Airway.共培养中的抑制作用:CF气道中相互拮抗关系对毒力和炎症的影响
Front Microbiol. 2018 Jun 5;9:1205. doi: 10.3389/fmicb.2018.01205. eCollection 2018.
2
Elevated IgG4 serum levels in patients with cystic fibrosis.囊性纤维化患者血清IgG4水平升高。
PLoS One. 2017 Sep 18;12(9):e0181888. doi: 10.1371/journal.pone.0181888. eCollection 2017.
3
Multivariate Analysis As a Support for Diagnostic Flowcharts in Allergic Bronchopulmonary Aspergillosis: A Proof-of-Concept Study.多变量分析作为变应性支气管肺曲霉病诊断流程图的支持:一项概念验证研究
Front Immunol. 2017 Aug 22;8:1019. doi: 10.3389/fimmu.2017.01019. eCollection 2017.
4
Secretory IgA response against Pseudomonas aeruginosa in the upper airways and the link with chronic lung infection in cystic fibrosis.上呼吸道对铜绿假单胞菌的分泌型 IgA 反应与囊性纤维化慢性肺部感染的关系。
Pathog Dis. 2017 Aug 31;75(6). doi: 10.1093/femspd/ftx069.
5
Global impact of bronchiectasis and cystic fibrosis.支气管扩张症和囊性纤维化的全球影响。
Breathe (Sheff). 2016 Sep;12(3):222-235. doi: 10.1183/20734735.007516.
6
Assessment of IgG antibodies to Pseudomonas aeruginosa in patients with cystic fibrosis by an enzyme-linked immunosorbent assay (ELISA).通过酶联免疫吸附测定(ELISA)评估囊性纤维化患者中针对铜绿假单胞菌的IgG抗体。
Diagn Pathol. 2014 Aug 22;9:158. doi: 10.1186/s13000-014-0158-z.
7
Adaptation of Pseudomonas aeruginosa in Cystic Fibrosis airways influences virulence of Staphylococcus aureus in vitro and murine models of co-infection.铜绿假单胞菌在囊性纤维化气道中的适应性影响金黄色葡萄球菌在体外和共感染小鼠模型中的毒力。
PLoS One. 2014 Mar 6;9(3):e89614. doi: 10.1371/journal.pone.0089614. eCollection 2014.
8
The impact of cystic fibrosis on the immunologic profile of pediatric patients.囊性纤维化对儿科患者免疫谱的影响。
J Pediatr (Rio J). 2013 Jan-Feb;89(1):40-7. doi: 10.1016/j.jped.2013.02.007.
9
Antibody orientation at bacterial surfaces is related to invasive infection.抗体在细菌表面的取向与侵袭性感染有关。
J Exp Med. 2012 Dec 17;209(13):2367-81. doi: 10.1084/jem.20120325. Epub 2012 Dec 10.
10
Secretory IgA as a diagnostic tool for Pseudomonas aeruginosa respiratory colonization.分泌型免疫球蛋白 A 作为铜绿假单胞菌呼吸道定植的诊断工具。
J Cyst Fibros. 2013 Jan;12(1):81-7. doi: 10.1016/j.jcf.2012.07.001. Epub 2012 Jul 20.

沙特阿拉伯囊性纤维化患者免疫球蛋白A、E、G和M水平的首份报告。

The first report on immunoglobulins A, E, G and M levels in cystic fibrosis patients in Saudi Arabia.

作者信息

Alothaid Hani, Banjar Hanaa, Kebir Fatuma M, Alharbi Abeer, Bin-Zuman Ghada

机构信息

Department of Basic Sciences, Faculty of Applied Medical Sciences, Al-Baha University, Al-Baha 1988, Saudi Arabia.

Department of Paediatrics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

出版信息

Saudi J Biol Sci. 2020 Oct;27(10):2617-2621. doi: 10.1016/j.sjbs.2020.05.041. Epub 2020 Jun 1.

DOI:10.1016/j.sjbs.2020.05.041
PMID:32994719
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7499114/
Abstract

BACKGROUND

Previous reports have shown that pulmonary and systemic hypergamma-globulinemia in CF patients is a reflection of chronic pulmonary infection. Infection with is known to have major prognostic significance in patients CF. This study aims to identify the incidence of immunoglobulins (especially: IgG, and IgE) in a cohort of CF patients.

METHODS

A total of 297 patients recruited all over the country's region for this study were a as part of the CF registry data from 1st January 1984 to 1st June 2016. All patients had their immunoglobulin levels measured by enzyme link immunosorbent assay (ELISA) in 3 stages, at presentation and two follow-ups.

RESULTS

Of the 297 patients recruited, 139 (46.8%) were males while 158 (53.2%) were females. IgA and IgM levels were found not to have risen above the previously reported levels in healthy individuals in all stages. On the contrary, IgE level increased from 209.51 ± 32.30 KU/L to 303.58 ± 37.11 KU/L from baseline to stage 3 while IgG level rose from 12.26 ± 0.43 mg/mL to 17.17 ± 1.68 mg/mL for baseline and stage 3 respectively all above previously reported levels in healthy individuals.

CONCLUSION

This study establishes a potential for the use of IgE and IgG in disease diagnosis as well as the prognostic implications. However, further study is needed to identify the role of infection or medications in relation to the rise of both IgE and IgG with advancement of age and progression of disease severity which may inherently confound the observed results.

摘要

背景

先前的报告表明,囊性纤维化(CF)患者的肺部和全身高丙种球蛋白血症是慢性肺部感染的一种表现。已知感染对CF患者具有重要的预后意义。本研究旨在确定一组CF患者中免疫球蛋白(尤其是IgG和IgE)的发生率。

方法

本研究共招募了来自全国该地区的297名患者,作为1984年1月1日至2016年6月1日CF登记数据的一部分。所有患者在就诊时及两次随访的3个阶段均通过酶联免疫吸附测定(ELISA)测量其免疫球蛋白水平。

结果

在招募的297名患者中,139名(46.8%)为男性,158名(53.2%)为女性。发现IgA和IgM水平在所有阶段均未高于先前报道的健康个体水平。相反,从基线到第3阶段,IgE水平从209.51±32.30 KU/L升至303.58±37.11 KU/L,而IgG水平分别从基线时的12.26±0.43 mg/mL升至第3阶段的17.17±1.68 mg/mL,均高于先前报道的健康个体水平。

结论

本研究确定了IgE和IgG在疾病诊断中的潜在用途及其预后意义。然而,需要进一步研究以确定感染或药物与随着年龄增长和疾病严重程度进展IgE和IgG升高之间的关系,这可能会固有地混淆观察结果。