Lee C A, Bofill M, Janossy G, Thomas H C, Rizza C R, Kernoff P B
Br J Haematol. 1985 May;60(1):161-72. doi: 10.1111/j.1365-2141.1985.tb07397.x.
Amongst 160 English haemophiliacs treated with clotting factor concentrates, abnormalities of T lymphocyte subset distribution (characterized by low T4/T8 ratios and high total T8 counts), low in vitro phytohaemagglutinin stimulation and raised serum IgG levels, were more common in patients with haemophilia A than B, in patients who had received heavier blood product exposure, and in adults rather than children. A slight reduction in lymphocyte and platelet counts was found in 26% and 17% of patients. In the sample of patients tested, serum alpha 1-thymosin levels were often raised, but beta 2-microglobulin levels were usually normal. Fractionation procedures used to prepare clotting factor concentrates, and the amounts of concentrate used, are more likely to be causally related to these immunological abnormalities than the origins of source donor plasmas.
在160例接受凝血因子浓缩物治疗的英国血友病患者中,T淋巴细胞亚群分布异常(以低T4/T8比值和高总T8计数为特征)、体外植物血凝素刺激低下和血清IgG水平升高,在甲型血友病患者中比乙型血友病患者更常见,在接受血液制品暴露量较大的患者中更常见,在成人中比儿童更常见。26%的患者淋巴细胞计数略有减少,17%的患者血小板计数略有减少。在检测的患者样本中,血清α1-胸腺素水平常升高,但β2-微球蛋白水平通常正常。用于制备凝血因子浓缩物的分级分离程序以及所使用的浓缩物量,比源供体血浆的来源更有可能与这些免疫异常存在因果关系。