Koike R, Takahashi H, Yoshida S
Division of Internal Medicine, Asahi General Hospital, Chiba.
Ryumachi. 1993 Feb;33(1):37-43.
We have studied the expression of OKT4-epitope on peripheral blood lymphocytes of 117 connective tissue disease patients and 72 normal controls. Three patients defected OKT4-epitope with a diagnosis of systemic lupus erythematosus (SLE). But they did not have any specific symptoms. The partial-deficiency patients with having as half as density of OKT4-epitope were found in SLE patients, other connective tissue disease patients and normal controls in a comparable proportion. Their mode of heredity was autosomal codominant as reported in the literature. And OKT4-epitope defective PBL reacted with mitogens normally. The relationship between OKT4-epitope deficiency and immunological disorder is not presently clarified. However, it might be relevant to study the role of OKT4-epitope in CD4 molecule in the pathogenesis of autoimmune disease.
我们研究了117例结缔组织病患者和72例正常对照者外周血淋巴细胞上OKT4表位的表达情况。3例系统性红斑狼疮(SLE)患者检测到OKT4表位缺陷,但无任何特异性症状。在SLE患者、其他结缔组织病患者和正常对照者中,发现OKT4表位密度仅为正常一半的部分缺陷患者比例相当。正如文献报道,其遗传方式为常染色体共显性。且OKT4表位缺陷的外周血淋巴细胞对有丝分裂原反应正常。目前尚不清楚OKT4表位缺陷与免疫紊乱之间的关系。然而,研究OKT4表位在CD4分子中在自身免疫性疾病发病机制中的作用可能具有相关性。