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肺炎球菌疫苗时代侵袭性肺炎球菌疾病患儿免疫缺陷的患病率:一项系统评价

Prevalence of Immunodeficiency in Children With Invasive Pneumococcal Disease in the Pneumococcal Vaccine Era: A Systematic Review.

作者信息

Butters Coen, Phuong Linny Kimly, Cole Theresa, Gwee Amanda

机构信息

Infectious Diseases Unit, The Royal Children's Hospital, Melbourne, Parkville, Australia.

Department of Allergy and Immunology, The Royal Children's Hospital, Melbourne, Parkville, Australia.

出版信息

JAMA Pediatr. 2019 Nov 1;173(11):1084-1094. doi: 10.1001/jamapediatrics.2019.3203.

Abstract

IMPORTANCE

Despite increasing access to vaccination, invasive pneumococcal disease (IPD) is responsible for approximately 826 000 deaths worldwide in children younger than 5 years each year. To allow early identification and prevention, an improved understanding of risk factors for IPD is needed.

OBJECTIVES

To review the literature on the prevalence of primary immunodeficiency (PID) in children younger than 18 years presenting with IPD without another predisposing condition and to inform guidelines for immunologic evaluation after the first episode of IPD based on published evidence.

EVIDENCE REVIEW

A literature search of PubMed, Embase (inception [1974] to February 28, 2019), and MEDLINE (inception [1946] to February 28, 2019) was conducted using the terms Streptococcus pneumonia, Streptococcus pneumoniae, pneumococcal infection, Streptococcus infection, pneumococcal meningitis, immunodeficiency, immune response, immunocompromised, susceptib*, precursor, predispose*, recurren*, newborn, neonat*, infan*, toddler, child, preschooler, adolescen*, and pediatric. Publications reporting original data on immunodeficiency in children with microbiologically confirmed primary or recurrent IPD were included. Strength of clinical data was graded according to the 5-point scale of the Oxford Centre for Evidence-Based Medicine.

FINDINGS

In 6022 unique children with primary IPD, 5 of 393 (1.3%) to 17 of 162 (10.5%) of all children and 14 of 53 (26.4%) of those older than 2 years had a PID identified. Higher rates of PID, up to 10 of 15 (66.7%), were found in children with recurrent IPD. Antibody deficiency was the most common immunodeficiency, followed by complement deficiency, asplenia, and rarer defects in T-cell signaling. The site of infection was a key indicator for the risk of underlying PID, with the greatest risk of PID in children with meningitis or complicated pneumonia.

CONCLUSIONS AND RELEVANCE

Results of this study suggest that invasive pneumococcal disease, and particularly recurrent IPD, is an important marker of underlying PID in children without other risk factors. The findings also suggest that children older than 2 years with pneumococcal meningitis or complicated pneumonia and all children with recurrent IPD should be referred for an immune evaluation.

TRIAL REGISTRATION

PROSPERO identifier: CRD42017075978.

摘要

重要性

尽管疫苗接种的可及性不断提高,但侵袭性肺炎球菌病(IPD)每年仍导致全球约82.6万名5岁以下儿童死亡。为了实现早期识别和预防,需要更好地了解IPD的危险因素。

目的

回顾关于无其他易感因素的18岁以下IPD患儿原发性免疫缺陷(PID)患病率的文献,并根据已发表的证据为IPD首次发作后的免疫评估指南提供参考。

证据综述

使用“肺炎链球菌”“肺炎链球菌感染”“链球菌感染”“肺炎球菌脑膜炎”“免疫缺陷”“免疫反应”“免疫受损”“易感性*”“前驱”“易患*”“复发*”“新生儿”“新生儿期*”“婴儿”“幼儿”“儿童”“学龄前儿童”“青少年*”和“儿科”等术语,对PubMed、Embase(创刊于1974年至2019年2月28日)和MEDLINE(创刊于1946年至2019年2月28日)进行文献检索。纳入报告微生物学确诊的原发性或复发性IPD患儿免疫缺陷原始数据的出版物。临床数据的强度根据牛津循证医学中心的5分制进行分级。

研究结果

在6022例原发性IPD患儿中,所有患儿中有393例中的5例(1.3%)至162例中的17例(10.5%),2岁以上患儿中有53例中的14例(26.4%)被确诊患有PID。复发性IPD患儿中PID的发生率更高,高达15例中的10例(66.7%)。抗体缺陷是最常见的免疫缺陷,其次是补体缺陷、无脾症以及T细胞信号传导方面较罕见的缺陷。感染部位是潜在PID风险的关键指标,患脑膜炎或复杂性肺炎的儿童患PID的风险最高。

结论及意义

本研究结果表明,侵袭性肺炎球菌病,尤其是复发性IPD,是无其他风险因素儿童潜在PID的重要标志。研究结果还表明,2岁以上患肺炎球菌脑膜炎或复杂性肺炎的儿童以及所有复发性IPD患儿均应转诊进行免疫评估。

试验注册

PROSPERO标识符:CRD42017075978。

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