Luckasen J R, Sabad A, Gajl-Peczalska K J, Kersey J H
Clin Exp Immunol. 1974 Apr;16(4):535-40.
Nine patients with primary immunodeficiency diseases were studied for the presence of lymphocytes bearing surface immunoglobulins, complement receptors, and sheep erythrocyte receptors. All were found to have a normal or increased percentage of lymphocytes bearing complement receptors, often despite a deficiency of immunoglobulin-bearing lymphocytes. The results suggest that these patients have a deficiency of surface immunoglobulin synthesis but are not deficient in B lymphocytes. Unsensitized sheep erythrocyte (E) binding (T) lymphocytes were normal or decreased; the sum of E-binding (T) plus complement receptor-bearing (B) lymphocytes was generally within the normal range. One exception was a patient with combined system immunodeficiency who had a decreased total of T plus B lymphocytes.
对9例原发性免疫缺陷病患者进行了研究,以检测携带表面免疫球蛋白、补体受体和绵羊红细胞受体的淋巴细胞的存在情况。结果发现,所有患者携带补体受体的淋巴细胞百分比正常或增加,尽管携带免疫球蛋白的淋巴细胞有所缺乏。这些结果表明,这些患者存在表面免疫球蛋白合成缺陷,但B淋巴细胞并不缺乏。未致敏的绵羊红细胞(E)结合(T)淋巴细胞正常或减少;E结合(T)淋巴细胞与携带补体受体(B)淋巴细胞的总和通常在正常范围内。唯一的例外是一名患有联合系统免疫缺陷的患者,其T加B淋巴细胞总数减少。