Alhumaid Saad, Al Mutared Koblan M, Al Alawi Zainab, Sabr Zainah, Alkhars Ola, Alabdulqader Muneera, Al Dossary Nourah, ALShakhs Fatemah M, Majzoub Rabab Abbas, Alalawi Yousef Hassan, Al Noaim Khalid, Alnaim Abdulrahman A, Al Ghamdi Mohammed A, Alahmari Abdulaziz A, Albattat Sawsan Sami, Almubarak Yasin S, Al Abdulmohsen Essam Mohammed, Al Shaikh Hanan, Alobaidan Mortadah Essa, Almusallam Hadi Hassan, Alhassan Fatimah Mohammed, Alamer Mohammed Abdulhadi, Al-Hajji Jawad Ali, Al-Hajji Duaa Ali, Alkadi Anwar Ahmed, Al Mutair Abbas, Rabaan Ali A
School of Pharmacy, University of Tasmania, Hobart, 7000, Australia.
Administration of Pharmaceutical Care, Ministry of Health, 66255, Najran, Saudi Arabia.
Allergy Asthma Clin Immunol. 2023 Aug 9;19(1):69. doi: 10.1186/s13223-023-00831-1.
Inborn errors of immunity (IEIs) are considered significant challenges for children with IEIs, their families, and their medical providers. Infections are the most common complication of IEIs and children can acquire coronavirus disease 2019 (COVID-19) even when protective measures are taken.
To estimate the incidence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in children with IEIs and analyse the demographic parameters, clinical characteristics and treatment outcomes in children with IEIs with COVID-19 illness.
For this systematic review, we searched ProQuest, Medline, Embase, PubMed, CINAHL, Wiley online library, Scopus and Nature through the Preferred Reporting Items for Systematic Reviews and Meta Analyses (PRISMA) guideline for studies on the development of COVID-19 in children with IEIs, published from December 1, 2019 to February 28, 2023, with English language restriction.
Of the 1095 papers that were identified, 116 articles were included in the systematic review (73 case report, 38 cohort 4 case-series and 1 case-control studies). Studies involving 710 children with IEIs with confirmed COVID-19 were analyzed. Among all 710 IEIs pediatric cases who acquired SARS-CoV-2, some children were documented to be admitted to the intensive care unit (ICU) (n = 119, 16.8%), intubated and placed on mechanical ventilation (n = 87, 12.2%), suffered acute respiratory distress syndrome (n = 98, 13.8%) or died (n = 60, 8.4%). Overall, COVID-19 in children with different IEIs patents resulted in no or low severity of disease in more than 76% of all included cases (COVID-19 severity: asymptomatic = 105, mild = 351, or moderate = 88). The majority of children with IEIs received treatment for COVID-19 (n = 579, 81.5%). Multisystem inflammatory syndrome in children (MIS-C) due to COVID-19 in children with IEIs occurred in 103 (14.5%). Fatality in children with IEIs with COVID-19 was reported in any of the included IEIs categories for cellular and humoral immunodeficiencies (n = 19, 18.6%), immune dysregulatory diseases (n = 17, 17.9%), innate immunodeficiencies (n = 5, 10%), bone marrow failure (n = 1, 14.3%), complement deficiencies (n = 1, 9.1%), combined immunodeficiencies with associated or syndromic features (n = 7, 5.5%), phagocytic diseases (n = 3, 5.5%), autoinflammatory diseases (n = 2, 3%) and predominantly antibody deficiencies (n = 5, 2.5%). Mortality was COVID-19-related in a considerable number of children with IEIs (29/60, 48.3%). The highest ICU admission and fatality rates were observed in cases belonging to cellular and humoral immunodeficiencies (26.5% and 18.6%) and immune dysregulatory diseases (35.8% and 17.9%) groups, especially in children infected with SARS-CoV-2 who suffered severe combined immunodeficiency (28.6% and 23.8%), combined immunodeficiency (25% and 15%), familial hemophagocytic lymphohistiocytosis (40% and 20%), X-linked lymphoproliferative diseases-1 (75% and 75%) and X-linked lymphoproliferative diseases-2 (50% and 50%) compared to the other IEIs cases.
Children with IEIs infected with SARS-CoV-2 may experience higher rates of ICU admission and mortality in comparison with the immunocompetent pediatric populations. Underlying immune defects does seem to be independent risk factors for severe SARS-CoV-2 infection in children with IEIs, a number of children with SCID and CID were reported to have prolonged infections-though the number of patients is small-but especially immune dysregulation diseases (XLP1 and XLP2) and innate immunodeficiencies impairing type I interferon signalling (IFNAR1, IFNAR2 and TBK1).
免疫缺陷病(IEIs)对患有免疫缺陷病的儿童、其家庭及其医疗服务提供者而言是重大挑战。感染是免疫缺陷病最常见的并发症,即使采取了防护措施,儿童仍可能感染2019冠状病毒病(COVID-19)。
评估免疫缺陷病儿童中严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染的发生率,并分析患有COVID-19疾病的免疫缺陷病儿童的人口统计学参数、临床特征和治疗结果。
对于本系统评价,我们通过系统评价和Meta分析的首选报告项目(PRISMA)指南,在ProQuest、Medline、Embase、PubMed、CINAHL、Wiley在线图书馆、Scopus和Nature中检索2019年12月1日至2023年2月28日发表的关于免疫缺陷病儿童COVID-19发病情况的研究,语言限制为英语。
在检索到的1095篇论文中,116篇文章纳入了系统评价(73篇病例报告、38篇队列研究、4篇病例系列研究和1篇病例对照研究)。对涉及710例确诊COVID-19的免疫缺陷病儿童的研究进行了分析。在所有710例感染SARS-CoV-2的免疫缺陷病儿科病例中,部分儿童被记录入住重症监护病房(ICU)(n = 119,16.8%)、接受插管并进行机械通气(n = 87,12.2%)、发生急性呼吸窘迫综合征(n = 98,13.8%)或死亡(n = 60,8.4%)。总体而言,在所有纳入病例中,超过76%的不同免疫缺陷病患儿感染COVID-19后疾病无或病情较轻(COVID-19严重程度:无症状 = 10例,轻度 = 351例,或中度 = 88例)。大多数免疫缺陷病儿童接受了COVID-19治疗(n = 579,81.5%)。免疫缺陷病儿童因COVID-19发生儿童多系统炎症综合征(MIS-C)的有103例(14.5%)。在细胞和体液免疫缺陷(n = 19,18.6%)、免疫失调疾病(n = 17,17.9%)、先天性免疫缺陷(n = 5,10%)、骨髓衰竭(n = 1,14.3%)、补体缺陷(n = 1,9.1%)、具有相关或综合征特征的联合免疫缺陷(n = 7,5.5%)、吞噬细胞疾病(n = 3,5.5%)、自身炎症性疾病(n = 2,3%)和主要抗体缺陷(n = 5,2.5%)等所有纳入的免疫缺陷病类别中,均有免疫缺陷病儿童感染COVID-19后死亡的报告。相当一部分免疫缺陷病儿童的死亡与COVID-19相关(29/60,48.3%)。在细胞和体液免疫缺陷组(26.5%和18.6%)以及免疫失调疾病组(35.8%和17.9%)的病例中,观察到最高的ICU入院率和死亡率,尤其是与其他免疫缺陷病病例相比,感染SARS-CoV--2的严重联合免疫缺陷儿童(28.6%和23.8%)、联合免疫缺陷儿童(25%和15%)、家族性噬血细胞性淋巴组织细胞增生症儿童(40%和20%)、X连锁淋巴增殖性疾病1型儿童(75%和75%)以及X连锁淋巴增殖性疾病2型儿童(50%和50%)。
与免疫功能正常的儿科人群相比,感染SARS-CoV-2的免疫缺陷病儿童可能有更高的ICU入院率和死亡率。潜在的免疫缺陷似乎是免疫缺陷病儿童发生严重SARS-CoV-2感染的独立危险因素,有报道称一些重症联合免疫缺陷(SCID)和联合免疫缺陷(CID)儿童感染时间延长,尽管患者数量较少,但尤其是免疫失调疾病(XLP1和XLP2)以及损害I型干扰素信号传导的先天性免疫缺陷(IFNAR1、IFNAR2和TBK1)。