Picard Capucine, Al-Herz Waleed, Bousfiha Aziz, Casanova Jean-Laurent, Chatila Talal, Conley Mary Ellen, Cunningham-Rundles Charlotte, Etzioni Amos, Holland Steven M, Klein Christoph, Nonoyama Shigeaki, Ochs Hans D, Oksenhendler Eric, Puck Jennifer M, Sullivan Kathleen E, Tang Mimi L K, Franco Jose Luis, Gaspar H Bobby
Laboratory of Human Genetics of Infectious Diseases, Necker Branch, INSERM UMR1163, Necker Hospital for Sick Children, Paris, France.
Centre d'étude des déficits immunitaires (CEDI), Hôpital Necker-Enfants Malades, AP-HP, Paris, France.
J Clin Immunol. 2015 Nov;35(8):696-726. doi: 10.1007/s10875-015-0201-1. Epub 2015 Oct 19.
We report the updated classification of primary immunodeficiencies compiled by the Primary Immunodeficiency Expert Committee (PID EC) of the International Union of Immunological Societies (IUIS). In the two years since the previous version, 34 new gene defects are reported in this updated version. For each disorder, the key clinical and laboratory features are provided. In this new version we continue to see the increasing overlap between immunodeficiency, as manifested by infection and/or malignancy, and immune dysregulation, as manifested by auto-inflammation, auto-immunity, and/or allergy. There is also an increased number of genetic defects that lead to susceptibility to specific organisms which reflects the finely tuned nature of immune defense systems. This classification is the most up to date catalogue of all known and published primary immunodeficiencies and acts as a current reference of the knowledge of these conditions and is an important aid for the genetic and molecular diagnosis of patients with these rare diseases.
我们报告了国际免疫学会联盟(IUIS)原发性免疫缺陷专家委员会(PID EC)编制的原发性免疫缺陷最新分类。自上一版发布后的两年里,本更新版报告了34种新的基因缺陷。对于每种疾病,均提供了关键的临床和实验室特征。在这个新版本中,我们继续看到免疫缺陷(表现为感染和/或恶性肿瘤)与免疫失调(表现为自身炎症、自身免疫和/或过敏)之间的重叠日益增加。导致对特定生物体易感性的基因缺陷数量也有所增加,这反映了免疫防御系统的精细调节特性。本分类是所有已知和已发表的原发性免疫缺陷的最新目录,是这些疾病知识的当前参考,也是对这些罕见病患者进行基因和分子诊断的重要辅助工具。