Maimaris Jesmeen, Payne Julia, Roa-Bautista Adriel, Breuer Judith, Storey Nathaniel, Morfopoulou Sofia, Bamford Alasdair, D'Arco Felice, Gilmour Kimberly, Aquilina Kristian, Hassell Jane, Hacohen Yael, Silva Adikarige H D, Merve Ashirwad, Jacques Thomas S, Rao Kanchan, Chiesa Robert, Amrolia Persis, Silva Juliana, Braggins Helen, Xu-Bayford Jinhua, Goldblatt David, Worth Austen, Booth Claire, Ip Winnie, Qasim Waseem, Kusters Maaike, Kaliakatsos Marios, Brown Julianne R, Elfeky Reem
Department of Immunology, Great Ormond Street Hospital for Children, NHS Foundation Trust, London, WC1N 3JH, UK.
University College London (UCL) Institute of Immunity and Transplantation, London, UK.
J Clin Immunol. 2025 Apr 16;45(1):86. doi: 10.1007/s10875-025-01878-y.
Unexplained neurological symptoms can pose a diagnostic challenge in patients with inborn errors of immunity (IEI) where the aetiology can be varied, and diverse pathologies may require contrasting treatments. Brain biopsy, the process of sampling brain tissue directly, has historically provided histological and microbiological information and can now be exploited for deep metagenomic next generation analysis (mNGS). We conducted a retrospective analysis of clinical and diagnostic data on paediatric patients with IEI who had a brain biopsy between 2010 and 2022 at a UK tertiary centre where 14 patients fulfilled our search criteria. We report on clinical characteristics, adverse events and the additional impact of mNGS of brain biopsies, where these were conducted. We found that brain biopsy enabled diagnostics with manageable complications in most cases, either by tissue or metagenomics analysis (n = 11/14, 79%). We found that mNGS analysis improved the diagnostic yield of brain biopsy in 29% of IEI cases (n = 4/14). Brain biopsy enabled a change in management in 71% of cases (n = 10/14). This series provides compelling evidence for the safe and purposeful use of brain biopsy in children with IEI.
不明原因的神经症状可能给先天性免疫缺陷(IEI)患者带来诊断挑战,其病因可能多种多样,不同的病理情况可能需要不同的治疗方法。脑活检,即直接获取脑组织样本的过程,历来可提供组织学和微生物学信息,现在还可用于深度宏基因组下一代分析(mNGS)。我们对2010年至2022年期间在英国一家三级中心接受脑活检的IEI儿科患者的临床和诊断数据进行了回顾性分析,其中14名患者符合我们的搜索标准。我们报告了临床特征、不良事件以及进行脑活检mNGS时的额外影响。我们发现,在大多数情况下,脑活检通过组织学或宏基因组学分析能够实现诊断,且并发症可控(n = 11/14,79%)。我们发现,mNGS分析在29%的IEI病例(n = 4/14)中提高了脑活检的诊断率。脑活检在71%的病例(n = 10/14)中促使了治疗方案的改变。该系列研究为在IEI儿童中安全且有目的地使用脑活检提供了有力证据。