Ersoy F, Sanal O, Tezcan I, Yel L, Metin A
Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara.
Turk J Pediatr. 1995 Apr-Jun;37(2):141-6.
Bare lymphocyte syndrome (BLS) is a rare disorder characterized by deficient expression of human leukocyte antigens (HLA antigens) and combined immunodeficiency to various degrees. Recurrent severe infections especially due to opportunistic organisms are common. Here, we present two patients with BLS who lack both class I and II antigens (Type III). They had the typical clinical and immunologic findings of BLS. The first patient showed marked improvement in pulmonary symptoms resulting from cytomegalovirus infection by means of gancyclovir treatment. However, intramuscular injections of interferon-alpha (IFN-alpha) had no beneficial effect in either the expression of HLA antigens or the clinical status. The second patient died of septicemia while being prepared for bone marrow transplantation.
裸淋巴细胞综合征(BLS)是一种罕见的疾病,其特征是人类白细胞抗原(HLA抗原)表达缺陷以及不同程度的联合免疫缺陷。反复发生严重感染,尤其是由机会性生物体引起的感染很常见。在此,我们报告两名I类和II类抗原均缺乏的BLS患者(III型)。他们具有BLS典型的临床和免疫学表现。首例患者通过更昔洛韦治疗,因巨细胞病毒感染导致的肺部症状有明显改善。然而,肌肉注射α干扰素(IFN-α)对HLA抗原表达或临床状况均无有益影响。第二例患者在准备进行骨髓移植时死于败血症。