Pohl W, Armbruster C, Bernhardt K, Drlicek M, Vetter N
Medizinische Abteilung, Pulmologisches Zentrum der Stadt Wien.
Wien Klin Wochenschr. 1995;107(3):95-100.
We report on two patients with idiopathic CD4+ T cell depletion. A 26 year-old woman presented to us with acute respiratory failure requiring mechanical ventilation. Despite combined antibiotic therapy parenterally the opacities increased in the chest X-ray. An open lung biopsy was performed and led to the histological diagnosis of bronchiolitis obliterans organizing pneumonia (BOOP). Respiratory function was improved impressively by high dose parenteral cortisone administration. This patient showed a general lymphocytopenia with severe CD4+ T cell depletion (60(37%)/mm3 blood). The CT4+ T cell concentration increased during a follow up period of 14 months, but did not reach normal values. The second patient was a 33 year-old homosexual. He was admitted with a mucocutaneous fungal infection which was successfully treated by antifungal drugs. This patient demonstrated a transient CD4+ T cell depletion (350(32%)/mm3 blood). In both patients HIV type 1 and 2 infections were excluded by antibody- and p 24-antigen testing, polymerase chain reaction and virus culture. CONCLUSION. Idiopathic CD4+ T lymphocytopenia differs from HIV infection in immunological profile, in the tendency to reversal of the CD4+ T cell depletion over time and in its better prognosis. It is unclear if this is a new syndrome and whether a transmissible agent, or possibly a genetically-determined reaction to noxious agents is responsible.
我们报告了两名特发性 CD4+ T 细胞耗竭患者。一名 26 岁女性因急性呼吸衰竭前来就诊,需要机械通气。尽管进行了联合静脉抗生素治疗,但胸部 X 光片上的肺部阴影仍增大。进行了开放性肺活检,组织学诊断为闭塞性细支气管炎伴机化性肺炎(BOOP)。高剂量静脉注射可的松使呼吸功能得到显著改善。该患者出现全身性淋巴细胞减少,伴有严重的 CD4+ T 细胞耗竭(血液中 CD4+ T 细胞计数为 60(37%)/mm³)。在 14 个月的随访期间,CD4+ T 细胞浓度有所增加,但未达到正常水平。第二名患者是一名 33 岁的同性恋者。他因皮肤黏膜真菌感染入院,经抗真菌药物治疗成功。该患者表现出短暂的 CD4+ T 细胞耗竭(血液中 CD4+ T 细胞计数为 350(32%)/mm³)。通过抗体和 p24 抗原检测、聚合酶链反应及病毒培养,排除了两名患者的 1 型和 2 型 HIV 感染。结论。特发性 CD4+ T 淋巴细胞减少在免疫特征、CD4+ T 细胞耗竭随时间逆转的趋势及其较好的预后方面与 HIV 感染不同。目前尚不清楚这是否是一种新综合征,以及是否由一种可传播因子或可能是对有害因子的基因决定反应所致。