因子替代对血友病患者b细胞反应的影响。

J Kekow, H Plendl, W L Gross
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引用次数: 0

摘要

血友病患者接受因子浓缩物的研究表明体外存在t细胞缺陷。最近,在艾滋病和艾滋病前期以及一些血友病患者中描述了b细胞功能障碍。为了研究血友病患者b细胞功能与因子替代的关系,我们检查了5例轻度(替代量小于20,000 U/年)和7例重度(大于100,000 U/年)血友病A患者,并将数据与正常对照个体进行了比较。体外研究了b细胞对金黄色葡萄球菌(Staphylococcus aureus Cowan I)的增殖反应(3h -胸苷摄取)和对t细胞依赖型或非依赖型多克隆b细胞激活剂(PBAs)的分化反应(Ig分泌到培养上清)。与t细胞功能障碍(与凝血因子浓度相关)相反,b细胞增殖反应不受影响。然而,PBAs刺激不能增加自发升高的IgG水平,并且在严重血友病中显示IgM水平的增加减少,而在轻度血友病中则没有。我们的数据表明,无症状血友病患者的t细胞不依赖b细胞功能障碍与因子替代相关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Influence of factor substitution on the B-cell response in hemophiliacs.

Studies in hemophiliacs receiving factor concentrates demonstrated T-cell defects in vitro. Recently, B-cell dysfunctions were described in AIDS and pre-AIDS and in some hemophiliacs. To investigate the B-cell function in hemophiliacs in relation to factor substitution, we examined five patients with mild (substitution less than 20,000 U/year) and seven with severe (greater than 100,000 U/year) hemophilia A and compared the data with normal control individuals. The B-cell proliferative response (3H-thymidine uptake) to Staphylococcus aureus Cowan I and the differentiation response (Ig secretion into culture supernatants) to T-cell-dependent or -independent polyclonal B-cell activators (PBAs) were studied in vitro. In contrast to T-cell dysfunctions, which correlate with the amount of clotting factor concentrates, the B-cell proliferative response was not affected. Stimulation with PBAs however failed to increase elevated spontaneous IgG levels and showed a diminished increase in IgM levels in severe, but not in mild, hemophilia. Our data give evidence of a T-cell-independent B-cell dysfunction in asymptomatic hemophiliacs that correlates with factor substitution.

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