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重症联合免疫缺陷病中B淋巴细胞分化的异质性

Heterogeneity of b lymphocyte differentiation in severe combined immunodeficiency disease.

作者信息

Pahwa S G, Pahwa R N, Good R A

出版信息

J Clin Invest. 1980 Sep;66(3):543-50. doi: 10.1172/JCI109886.

Abstract

Pokeweed mitogen-induced B lymphocyte differentiation in vitro into antibody secreting plaque-forming cells (PFC) was investigated in nine patients with severe combined immunodeficiency having variable proportions of circulating B lymphocytes. When cultured by themselves, the peripheral blood mononuclear cells did not respond to stimulation with pokeweed mitogen in any patient. In the presence of irradiated allogeneic T cells as helpers, however, PFC responses were elicited in lymphocyte cultures from peripheral blood and/or bone marrow in some patients. In one of these patients, results of allogeneic co-culture experiments were suggestive of genetically restricted suppressor cells. In a single patient with deficiency of the enzyme adenosine deaminase, PFC were generated in bone marrow lymphocyte cultures only when they were supplemented with exogenous adenosine deaminase and allogeneic helper cells. A parallel study of T lymphocyte differentiation in vitro performed in fractionated bone marrow cells was suggestive of arrested differentiation at different steps along the differentiation pathway. In two patients with evidence of functional B cell precursors, deficiencies of helper T cell function could be attributed to differentiation defects at the level of the stem cells in one and the thymus in the other. The findings reported here further substantiate the heterogeneity of the severe combined immunodeficiency disease syndromes.

摘要

在9例循环B淋巴细胞比例各异的严重联合免疫缺陷患者中,研究了商陆有丝分裂原诱导B淋巴细胞在体外分化为抗体分泌性空斑形成细胞(PFC)的情况。当外周血单个核细胞单独培养时,任何患者的细胞对商陆有丝分裂原刺激均无反应。然而,在存在经照射的同种异体T细胞作为辅助细胞的情况下,部分患者外周血和/或骨髓淋巴细胞培养物中可引发PFC反应。在其中1例患者中,同种异体共培养实验结果提示存在基因限制性抑制细胞。在1例腺苷脱氨酶缺乏的患者中,骨髓淋巴细胞培养物仅在补充外源性腺苷脱氨酶和同种异体辅助细胞时才产生PFC。在对分离的骨髓细胞进行的体外T淋巴细胞分化的平行研究中,提示在分化途径的不同步骤存在分化停滞。在2例有功能性B细胞前体证据的患者中,辅助性T细胞功能缺陷在1例可归因于干细胞水平的分化缺陷,在另1例可归因于胸腺水平的分化缺陷。此处报告的研究结果进一步证实了严重联合免疫缺陷疾病综合征的异质性。

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