Seeger R C, Robins R A, Stevens R H, Klein R B, Waldman D J, Zeltzer P M, Kessler S W
Clin Exp Immunol. 1976 Oct;26(1):1-10.
A 6 1/2-month-old male with severe combined immunodeficiency (SCID) had a low percentage and number of T cells (11%; 241/mm3) and a high percentage and number of B cells (52%; 1187/mm3) and null cells (37%; 868/mm3). In vitro studies were performed to determine if this child's primary defect involved differentiation of both T and B lymphocytes or if failure of B lymphocytes to differentiate into immunoglobulin producing cells was secondary to T lymphocyte abnormalities. Immunoglobulin production by lymphocytes in response to polyclonal mitogens (pokeweed mitogen and foetal calf serum) was measured by pulse-labelling cells with 3H-leucine and then precipitating cytoplasmic and secreted immunoglobulins with polyvalent anti-human immunoglobulin and S. aureus (Cowan strain I) protein A. The patient's lymphocytes did not synthesize immunoglobulins in vitro in response to mitogens. They did not suppress synthesis of immunoglobulins by normal lymphocytes. However, addition of normal purified T cells, which themselves did not synthesize immunoglobulins, enabled the patient's B lymphocytes to become immunoglobulin synthesizing and secreting cells. Gamma, mu, and light chains were secreted. This suggests that the primary abnormality was in the T-cell axis at the level of lymphoid stem cells or prothymocytes and that failure of B lymphocytes to become immunoglobulin-producing cells was secondary to this defect.
一名6个半月大的患有严重联合免疫缺陷(SCID)的男婴,其T细胞的百分比和数量较低(11%;241/mm³),B细胞的百分比和数量较高(52%;1187/mm³),裸细胞的百分比和数量也较高(37%;868/mm³)。进行了体外研究,以确定该患儿的原发性缺陷是涉及T和B淋巴细胞的分化,还是B淋巴细胞未能分化为产生免疫球蛋白的细胞是继发于T淋巴细胞异常。通过用³H-亮氨酸脉冲标记细胞,然后用多价抗人免疫球蛋白和金黄色葡萄球菌(考恩I株)蛋白A沉淀细胞质和分泌的免疫球蛋白,来测量淋巴细胞对多克隆有丝分裂原(商陆有丝分裂原和胎牛血清)的免疫球蛋白产生情况。该患者的淋巴细胞在体外对有丝分裂原无反应,不合成免疫球蛋白。它们也不抑制正常淋巴细胞的免疫球蛋白合成。然而,加入本身不合成免疫球蛋白的正常纯化T细胞后,患者的B淋巴细胞能够成为免疫球蛋白合成和分泌细胞,并分泌γ、μ和轻链。这表明原发性异常在于淋巴干细胞或原胸腺细胞水平的T细胞轴,B淋巴细胞未能成为产生免疫球蛋白的细胞是继发于这一缺陷。