Gehrz R C, McAuliffe J J, Linner K M, Kersey J H
Clin Exp Immunol. 1980 Feb;39(2):344-8.
We report a girl with severe combined immunodeficiency with functional impairment of both humoral and cellular immunity despite normal numbers of B and T lymphocytes. Immunologic studies revealed hypergammaglobulinaemia, absent migratory response by polymorphonuclear leucocytes to chemoattractants, and diminished lymphocyte proliferative responses to mitogens, antigens and allogeneic leucocytes. However, stimulation of the patient's mononuclear leucocytes with the calcium ionophore, A23187, resulted in a normal proliferative response. We therefore postulate a membrane defect as the basis for immunologic dysfunction in this child.
我们报告了一名患有严重联合免疫缺陷的女孩,尽管其B淋巴细胞和T淋巴细胞数量正常,但体液免疫和细胞免疫均存在功能障碍。免疫学研究显示,该女孩存在高球蛋白血症,多形核白细胞对趋化因子无迁移反应,淋巴细胞对有丝分裂原、抗原和同种异体白细胞的增殖反应减弱。然而,用钙离子载体A23187刺激该患者的单核白细胞可导致正常的增殖反应。因此,我们推测膜缺陷是该患儿免疫功能障碍的基础。