Warnatz K, Draeger R, Schlesier M, Peter H H
Department of Internal Medicine, University Hospital Freiburg, Germany.
Immunobiology. 2000 Aug;202(2):204-11. doi: 10.1016/S0171-2985(00)80068-6.
Idiopathic CD4+ T lymphocytopenia (ICL) has been defined by the center of disease control as a rare cause of immunodeficiency with a variable clinical course and an unknown aetiology. Here we describe a 65-year old patient with relapsing generalized herpes zoster infection due to ICL and a severe panlymphocytopenia. In vitro assays revealed an enhanced activation of CD8+ T cells and an increased sensitivity of activated CD4+ T cells for cell death. The clinical outcome was substantially improved after starting the patient on a subcutaneous therapy with IL-2.
特发性CD4 + T淋巴细胞减少症(ICL)已被疾病控制中心定义为一种罕见的免疫缺陷病因,其临床病程多变且病因不明。在此,我们描述了一名65岁因ICL导致复发性全身性带状疱疹感染并伴有严重全淋巴细胞减少症的患者。体外试验显示CD8 + T细胞激活增强,活化的CD4 + T细胞对细胞死亡的敏感性增加。在开始对该患者进行皮下注射IL-2治疗后,临床结果有了显著改善。