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Clin Exp Immunol. 1979 Nov;38(2):306-15.
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本文引用的文献

1
Studies on the serum gamma-A-globulin level. 3. The frequency of A-gamma-A-globulinemia.血清γ-A球蛋白水平的研究。3. A-γ-A球蛋白血症的发生率。
Scand J Clin Lab Invest. 1965;17(4):316-20. doi: 10.3109/00365516509077057.
2
General methods for the study of cells and serum during the immune response: the response to dinitrophenyl in mice.免疫反应过程中细胞与血清研究的一般方法:小鼠对二硝基苯基的反应
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Differentiation capacity of cultured B lymphocytes from immunodeficient patients.免疫缺陷患者培养的B淋巴细胞的分化能力。
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A new and simple radioimmunoassay method for the determination of IgE.一种用于测定IgE的新型简易放射免疫测定方法。
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Role of suppressor T cells in pathogenesis of common variable hypogammaglobulinaemia.抑制性T细胞在常见变异型低丙种球蛋白血症发病机制中的作用。
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Cell surface markers for human T and B lymphocytes.人类T淋巴细胞和B淋巴细胞的细胞表面标志物。
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7
Cell surface immunoglobulin. XI. The appearance of an IgD-like molecule on murine lymphoid cells during ontogeny.细胞表面免疫球蛋白。XI. 小鼠淋巴样细胞个体发育过程中类IgD分子的出现。
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8
Defect in IgA secretion and in IgA specific suppressor cells in patients with selective IgA deficiency.选择性IgA缺乏症患者的IgA分泌及IgA特异性抑制细胞缺陷。
Trans Assoc Am Physicians. 1976;89:215-24.
9
The effects of purified mitogenic proteins (Pa-1 and Pa-2) from pokeweed on human T and B lymphocytes in vitro.商陆纯化促有丝分裂蛋白(Pa - 1和Pa - 2)对人T淋巴细胞和B淋巴细胞的体外作用
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10
The role of suppressor cells in the pathogenesis of common variable hypogammaglobulinemia and the immunodeficiency associated with myeloma.抑制细胞在常见变异型低丙种球蛋白血症发病机制及与骨髓瘤相关免疫缺陷中的作用。
Fed Proc. 1976 Jul;35(9):2067-72.

来自正常和选择性IgA缺乏受试者的外周血单个核细胞的IgA合成

IgA synthesis by peripheral blood mononuclear cells from normal and selectively IgA deficient subjects.

作者信息

King M A, Wells J V, Nelson D S

出版信息

Clin Exp Immunol. 1979 Nov;38(2):306-15.

PMID:527265
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1537868/
Abstract

IgA secretion and intracellular IgA synthesis by PWM-stimulated peripheral blood lymphocytes from normal and IgA deficient subjects were measured by radioimmunoassay. Cultured lymphocytes from eleven out of twelve IgA deficient subjects had impaired or undetectable IgA production. Measurement of intracellular IgA showed that the defect was more basic than simply defective secretion by IgA plasma cells. Co-culture of lymphocytes from IgA deficient and normal subjects revealed defects in both the B and T cell populations of IgA deficient subjects. In one subject the defect was in the T cells, in another the B cells, and in two others both T and B cells were defective.

摘要

通过放射免疫测定法测量了来自正常和IgA缺陷受试者的经PWM刺激的外周血淋巴细胞的IgA分泌和细胞内IgA合成。12名IgA缺陷受试者中有11名的培养淋巴细胞存在IgA产生受损或无法检测到的情况。细胞内IgA的测量表明,该缺陷比单纯的IgA浆细胞分泌缺陷更为根本。IgA缺陷和正常受试者的淋巴细胞共培养显示IgA缺陷受试者的B细胞和T细胞群体均存在缺陷。在一名受试者中缺陷存在于T细胞,在另一名受试者中存在于B细胞,在另外两名受试者中T细胞和B细胞均有缺陷。