Division of Rheumatology, Universidade Federal de São Paulo, Sao Paulo, Brazil.
Immunology Division, Fleury Medicine and Health Laboratory, Sao Paulo, Brazil.
Front Immunol. 2021 Nov 9;12:721289. doi: 10.3389/fimmu.2021.721289. eCollection 2021.
Inborn errors of immunity (IEI), which were previously termed primary immunodeficiency diseases, represent a large and growing heterogeneous group of diseases that are mostly monogenic. In addition to increased susceptibility to infections, other clinical phenotypes have recently been associated with IEI, such as autoimmune disorders, severe allergies, autoinflammatory disorders, benign lymphoproliferative diseases, and malignant manifestations. The IUIS 2019 classification comprises 430 distinct defects that, although rare individually, represent a group affecting a significant number of patients, with an overall prevalence of 1:1,200-2,000 in the general population. Early IEI diagnosis is critical for appropriate therapy and genetic counseling, however, this process is deeply dependent on accurate laboratory tests. Despite the striking importance of laboratory data for clinical immunologists, several IEI-relevant immunoassays still lack standardization, including standardized protocols, reference materials, and external quality assessment programs. Moreover, well-established reference values mostly remain to be determined, especially for early ages, when the most severe conditions manifest and diagnosis is critical for patient survival. In this article, we intend to approach the issue of standardization and quality control of the nonfunctional diagnostic tests used for IEI, focusing on those frequently utilized in clinical practice. Herein, we will focus on discussing the issues of nonfunctional immunoassays (flow cytometry, enzyme-linked immunosorbent assays, and turbidimetry/nephelometry, among others), as defined by the pure quantification of proteins or cell subsets without cell activation or cell culture-based methods.
先天性免疫缺陷(IEI),以前称为原发性免疫缺陷病,代表了一组庞大且不断增长的异质性疾病,这些疾病主要是单基因疾病。除了易感染外,最近还与 IEI 相关联的其他临床表型,如自身免疫性疾病、严重过敏、自身炎症性疾病、良性淋巴增生性疾病和恶性表现。IUIS 2019 分类包括 430 种不同的缺陷,尽管每种缺陷都很罕见,但它们代表了一组影响大量患者的疾病,在普通人群中的总体患病率为 1:1200-2000。早期 IEI 诊断对于适当的治疗和遗传咨询至关重要,但这一过程严重依赖于准确的实验室测试。尽管实验室数据对临床免疫学家具有重要意义,但仍有许多与 IEI 相关的免疫测定缺乏标准化,包括标准化的方案、参考物质和外部质量评估计划。此外,建立良好的参考值大多仍有待确定,特别是在年龄最小的时候,因为最严重的疾病表现出来,诊断对于患者的生存至关重要。在本文中,我们旨在探讨用于 IEI 的非功能性诊断测试的标准化和质量控制问题,重点关注那些在临床实践中经常使用的测试。在此,我们将重点讨论非功能性免疫测定(流式细胞术、酶联免疫吸附测定和比浊/散射光度法等)的问题,这些问题是通过纯蛋白质或细胞亚群的定量来定义的,而不进行细胞激活或基于细胞培养的方法。