Optimising immunisation in children with 22q11 microdeletion.

Q2 Medicine Therapeutic Advances in Vaccines and Immunotherapy Pub Date : 2020-10-16 eCollection Date: 2020-01-01 DOI:10.1177/2515135520957139
Angela Berkhout, Kahn Preece, Vanil Varghese, Vinita Prasad, Helen Heussler, Julia Clark, Sophie C H Wen
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引用次数: 2

Abstract

Background: The condition known as 22q11 microdeletion syndrome has a broad phenotypic spectrum, with many affected individuals experiencing mild-to-moderate immunodeficiency. Currently, there are significant variations in live vaccine practices and immunological testing prior to live vaccine administration due to safety concerns and limited established guidelines.

Methods: Queensland Children's Hospital (QCH) Child Development Unit, offers a state-wide 22q11 microdeletion clinic. This is a retrospective single-centre review, capturing the majority of children with 22q11 microdeletion in Queensland, Australia. We describe the live vaccination status of 134 children, age 0 to 18 years under our care between 2000 and 2018, adverse events following immunisation (AEFI) and the proportion of children who received additional pneumococcal coverage. An immunological investigation pathway prior to live vaccine administration is proposed.

Results: Of the 134 children, 124 were eligible for live vaccinations as per the Australian National Immunisation Program: 82% had received dose one of measles, mumps and rubella (MMR) vaccine, 77% had completed MMR dose two and 66% had completed varicella immunisation. There were no AEFI notifications reported. Of the total sample of children, 18% received a fourth dose of conjugate pneumococcal vaccine (Prevenar 7 or 13) and 16% received a dose of Pneumovax 23 from 4 years of age. Immunology workup practices were demonstrated to vary widely prior to live vaccine administration. Most patients' immune profiles were consistent with mild-to-moderate immunodeficiency.

Conclusion: We propose an immunological investigation and vaccination pathway with the aim of providing guidance and consistency to clinicians caring for children with 22q11 microdeletion.

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22q11微缺失儿童免疫优化
背景:22q11微缺失综合征具有广泛的表型谱,许多受影响的个体经历轻度至中度免疫缺陷。目前,由于安全问题和有限的既定指南,在活疫苗实践和接种活疫苗前的免疫检测方面存在重大差异。方法:昆士兰州儿童医院(QCH)儿童发展科,提供一个全国性的22q11微缺失诊所。这是一项回顾性单中心综述,在澳大利亚昆士兰州捕获了22q11微缺失的大多数儿童。我们描述了2000年至2018年期间在我们护理下的134名0至18岁儿童的活疫苗接种状况、免疫后不良事件(AEFI)以及获得额外肺炎球菌覆盖的儿童比例。提出了活疫苗接种前的免疫调查途径。结果:在134名儿童中,124名符合澳大利亚国家免疫计划的活疫苗接种条件:82%接种了麻疹、腮腺炎和风疹(MMR)疫苗的第一剂,77%完成了MMR疫苗的第二剂,66%完成了水痘免疫。无AEFI报告。在全部儿童样本中,18%接受了第四剂结合肺炎球菌疫苗(Prevenar 7或13),16%从4岁开始接受了一剂Pneumovax 23。在接种活疫苗之前,免疫学检查实践被证明差异很大。大多数患者的免疫特征与轻度至中度免疫缺陷一致。结论:我们提出了一种免疫学调查和疫苗接种途径,旨在为临床医生护理22q11微缺失儿童提供指导和一致性。
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来源期刊
Therapeutic Advances in Vaccines and Immunotherapy
Therapeutic Advances in Vaccines and Immunotherapy Medicine-Pharmacology (medical)
CiteScore
5.10
自引率
0.00%
发文量
15
审稿时长
8 weeks
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