Pyke K W, Dosch H, Ipp M M, Gelfand E W
N Engl J Med. 1975 Aug 28;293(9):424-8. doi: 10.1056/NEJM197508282930904.
An in vitro system has been developed to elucidate the nature of the cellular defect in primary immunodeficiency diseases. Incubation, on human thymic epithelial monolayer cultures, of peripheral blood lymphocytes and bone-marrow cells from a child with documented severe combined immunodeficiency disease resulted in the appearance of a population of cells that formed rosettes with sheep erythrocytes. The same cell preparation permitted the synthesis of antigen-specific, complement-dependent antibodies after in vitro education, as demonstrated in a plaque assay system. In addition, thymic tissue from the same child gave morphologic and functional evidence of maturation when cultured in vitro. The experimental results suggest that in this case, lymphoid precursor cells were present in the bone marrow but failed to differentiate to functional maturity due to a defect in maturation of thymic tissue.
已开发出一种体外系统,以阐明原发性免疫缺陷疾病中细胞缺陷的本质。将一名患有确诊严重联合免疫缺陷疾病儿童的外周血淋巴细胞和骨髓细胞,在人胸腺上皮单层培养物上进行孵育,结果出现了一群能与绵羊红细胞形成玫瑰花结的细胞。如在空斑测定系统中所证实的,同样的细胞制剂在体外培养后能合成抗原特异性、补体依赖性抗体。此外,同一儿童的胸腺组织在体外培养时呈现出成熟的形态学和功能证据。实验结果表明,在这种情况下,骨髓中存在淋巴样前体细胞,但由于胸腺组织成熟缺陷而未能分化至功能成熟。