Department of Infectious Diseases, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, Aarhus University, Aarhus, Denmark.
Br J Haematol. 2019 Aug;186(3):471-476. doi: 10.1111/bjh.15947. Epub 2019 May 20.
MonoMAC is a complex primary immunodeficiency caused by mutations in the myeloid transcription factor GATA2, characterized by multilineage cytopenia with malignant complications and severe infections, including mycobacteria and herpesviruses. We describe the clinical presentation, genetics and antiviral inflammatory responses in a small case series. Two patients presented in childhood with mycobacterial infection and were diagnosed with MonoMAC germline GATA2 variants; their healthy fathers with the same mutations were also studied. Three patients were elderly individuals with acquired GATA2 mutations and malignant haematological conditions. Overall, this study demonstrates the heterogeneous clinical presentation and variation in immunodeficiency caused by GATA2 mutations.
MonoMAC 是一种由髓系转录因子 GATA2 突变引起的复杂原发性免疫缺陷病,其特征是多谱系细胞减少症伴有恶性并发症和严重感染,包括分枝杆菌和疱疹病毒。我们描述了一个小病例系列的临床表现、遗传学和抗病毒炎症反应。两名患者在儿童期出现分枝杆菌感染,并被诊断为 MonoMAC 种系 GATA2 变异;他们携带相同突变的健康父亲也接受了研究。三名患者为老年个体,患有获得性 GATA2 突变和恶性血液学疾病。总的来说,这项研究表明 GATA2 突变引起的临床表现和免疫缺陷的异质性。